ChemicalBook > CAS DataBase List > (S)-(+)-3-Hydroxytetrahydrofuran

(S)-(+)-3-Hydroxytetrahydrofuran

Product Name
(S)-(+)-3-Hydroxytetrahydrofuran
CAS No.
86087-23-2
Chemical Name
(S)-(+)-3-Hydroxytetrahydrofuran
Synonyms
(S)-TETRAHYDROFURAN-3-OL;(S)-3-HYDROXYTETRAHYDROFURAN;(3S)-oxolan-3-ol;(3S)-Tetrahydrofuran-3-ol;(S)-(-)-3-HYDROXY TETRAHYDRO FURAN;Oxolane-3β-ol;(S)-Hydroxy THF;Afatinib intermediate;S-3- Hydroxytetrafuran;Afatinib intermediate B
CBNumber
CB2142463
Molecular Formula
C4H8O2
Formula Weight
88.11
MOL File
86087-23-2.mol
More
Less

(S)-(+)-3-Hydroxytetrahydrofuran Property

Boiling point:
80 °C/15 mmHg (lit.)
alpha 
18.5 º (c=2 MeOH)
Density 
1.103 g/mL at 25 °C (lit.)
vapor pressure 
47Pa at 25℃
refractive index 
n20/D 1.45(lit.)
Flash point:
175 °F
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
Chloroform, Methanol (Slightly)
pka
14.49±0.20(Predicted)
form 
Liquid
Specific Gravity
1.11
color 
Clear colorless to pale yellow
optical activity
[α]20/D +17.5°, c = 2.4 in methanol
Water Solubility 
soluble
BRN 
4652609
Stability:
Stable. Combustible. Incompatible with strong oxidizing agents.
InChIKey
XDPCNPCKDGQBAN-BYPYZUCNSA-N
LogP
-0.784 at 22℃ and pH6.8
Surface tension
72mN/m at 1g/L and 25℃
CAS DataBase Reference
86087-23-2(CAS DataBase Reference)
More
Less

Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39
RIDADR 
NA 1993 / PGIII
WGK Germany 
3
HS Code 
29321900
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
296686
Product name
(S)-(+)-3-Hydroxytetrahydrofuran
Purity
99%
Packaging
5g
Price
$25.52
Updated
2024/03/01
Sigma-Aldrich
Product number
296686
Product name
(S)-(+)-3-Hydroxytetrahydrofuran
Purity
99%
Packaging
25g
Price
$104
Updated
2024/03/01
TCI Chemical
Product number
T1716
Product name
(S)-3-Hydroxytetrahydrofuran
Purity
>98.0%(GC)
Packaging
1g
Price
$16
Updated
2024/03/01
TCI Chemical
Product number
T1716
Product name
(S)-3-Hydroxytetrahydrofuran
Purity
>98.0%(GC)
Packaging
5g
Price
$38
Updated
2024/03/01
Alfa Aesar
Product number
H56476
Product name
(S)-(+)-3-Hydroxytetrahydrofuran, 98%
Packaging
5g
Price
$77.65
Updated
2024/03/01
More
Less

(S)-(+)-3-Hydroxytetrahydrofuran Chemical Properties,Usage,Production

Description

(S)-(+)-3-Hydroxytetrahydrofuran (3-OH THF) is a colorless liquid with a normal boiling point of 179 °C and boiling at 88-89 °C at 17 mmHg, with density (1.087 g/cm3 at 19 °C). 3-OH THF is a useful pharmaceutical intermediate. The chiral (absolute configuration S) version of this compound is an intermediate to launched retroviral drugs.

Chemical Properties

Colourless Liquid

Uses

(S)-(+)-3-Hydroxytetrahydrofuran is a useful reagent for the preparation of pyrazolo triazin ylamine derivatives as adenosine receptor antagonists.

Uses

(S)-(+)-3-Hydroxytetrahydrofuran is an intermediate to the AIDS drugs amprenavir and fosamprenavir. Additionally, it has been an intermediate to developmental drug substances, such as chemotherapy agents.

Synthesis

(S)-(+)-3-Hydroxytetrahydrofuran was prepared from the reaction of (S)-1,2,4-butanetriol under hydrochloric acid modified montmorillonite catalyst. The steps were as follows:To the heatable reactor (with stirring device), 100g (S)-1,2,4-butanetriol, 200mL toluene, 15g hydrochloric acid modified montmorillonite catalyst prepared in were added successively. The reaction was stopped after 4 h at 110°C. After the reaction is finished, it is naturally cooled to room temperature, and the obtained material is filtered to recover the catalyst. After collecting the filtrate, the remaining solvent and by-product water in the filtrate are distilled off to obtain (S)-3-hydroxytetrahydrofuran crude product. Quantitative analysis was carried out by gas chromatography, and the yield was 96.8%. Finally, the (S)-3-hydroxytetrahydrofuran was obtained by rectification and purification.

(S)-(+)-3-Hydroxytetrahydrofuran Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

(S)-(+)-3-Hydroxytetrahydrofuran Suppliers

HBCChem, Inc.
Tel
+1-510-219-6317
Fax
+1-650-486-1361
Email
sales@hbcchem.com
Country
United States
ProdList
10648
Advantage
60
Accela ChemBio Inc.
Tel
+1(858) 699-3322
Fax
+1(858) 876-1948
Email
marketing@accelachem.com
Country
United States
ProdList
6024
Advantage
65
Alfa Chemistry
Tel
1-516-6625404
Fax
1-516-927-0118
Email
support@alfa-chemistry.com
Country
United States
ProdList
9171
Advantage
60
AbaChemScene
Tel
732-484-9848
Fax
888-484-5008
Email
sales@chemscene.com
Country
United States
ProdList
3982
Advantage
60
Alfa Chemistry
Tel
Fax
1-516-927-0118
Email
Info@alfa-chemistry.com
Country
United States
ProdList
24072
Advantage
58
Accela ChemBio Inc.
Tel
+1-858-6993322
Fax
(+1)-858-876-1948
Email
info@accelachem.com
Country
United States
ProdList
17322
Advantage
58
Alchem Pharmtech,Inc.
Tel
8485655694
Email
sales@alchempharmtech.com
Country
United States
ProdList
63687
Advantage
58
Protheragen-ING
Tel
+16313385890
Email
info@protheragen-ing.com
Country
United States
ProdList
3868
Advantage
58
Aladdin Scientific
Tel
+1-+1(833)-552-7181
Email
sales@aladdinsci.com
Country
United States
ProdList
57505
Advantage
58
Synthonix Inc
Tel
--
Fax
--
Email
info@synthonix.com
Country
United States
ProdList
6872
Advantage
58
Alfa Chemistry
Tel
--
Fax
--
Email
info@Alfa-Chemistry.com
Country
United States
ProdList
6814
Advantage
0
CarboMer, Inc.
Tel
--
Fax
--
Email
sales@carbomer.com
Country
United States
ProdList
4026
Advantage
67
Combi-Blocks, Inc.
Tel
--
Fax
--
Email
les@combi-blocks.com
Country
United States
ProdList
2555
Advantage
58
Kaneka America LLC (part of Kaneka Corporation Japan)
Tel
--
Fax
--
Email
alexis.mercado@kaneka.com
Country
United States
ProdList
51
Advantage
58
Fluorochem Ltd.
Tel
--
Fax
--
Email
enquiries@fluorochem.co.uk
Country
United States
ProdList
4583
Advantage
58
MilliporeSigma (Sigma-Aldrich Corp.)
Tel
--
Fax
--
Email
@sial.com
Country
United States
ProdList
5414
Advantage
58
Alichem Inc.
Tel
--
Fax
--
Email
sales@alichem.com
Country
United States
ProdList
6167
Advantage
58
Synblock,Inc.
Tel
--
Fax
--
Email
sales@synblock.com
Country
United States
ProdList
228
Advantage
58
2A Biotech USA
Tel
--
Fax
--
Email
info@2abiotech.com
Country
United States
ProdList
1785
Advantage
58
Accela ChemBio Inc.
Tel
--
Fax
--
Email
info@accelachem.com
Country
United States
ProdList
1054
Advantage
50
JR MediChem LLC
Tel
--
Fax
--
Email
sales@jrmedichem.com
Country
United States
ProdList
86
Advantage
0
TCI America, Inc. (part of Tokyo Chemical Industry)
Tel
--
Fax
--
Email
Angelina.Crew@tcichemicals.com
Country
United States
ProdList
2053
Advantage
58
OChem Incorporation
Tel
--
Fax
--
Email
sales@ocheminc.com
Country
United States
ProdList
6501
Advantage
60
Oakwood Products, Inc.
Tel
--
Fax
--
Email
sales@oakwoodchemical.com
Country
United States
ProdList
6193
Advantage
74
Riedel-de Haen AG
Tel
--
Fax
--
Country
United States
ProdList
6773
Advantage
87
TCI America
Tel
--
Fax
--
Email
sales@tciamerica.com
Country
United States
ProdList
6909
Advantage
75
Frontier Scientific, Inc.
Tel
--
Fax
--
Email
sales@frontiersci.com
Country
United States
ProdList
6222
Advantage
86
Matrix Scientific
Tel
--
Fax
--
Email
sales@matrixscientific.com
Country
United States
ProdList
6632
Advantage
80
CacheSyn Inc.
Tel
--
Fax
--
Email
info@cachesyn.com
Country
United States
ProdList
695
Advantage
50
HBCChem, Inc.
Tel
--
Fax
--
Email
Sales@hbcchem-inc.com
Country
United States
ProdList
887
Advantage
50
Small Molecules, Inc.
Tel
--
Fax
--
Email
sales@small-molecules.com
Country
United States
ProdList
1218
Advantage
30
Ivy Fine Chemicals
Tel
--
Fax
--
Email
sales@ivychem.com
Country
United States
ProdList
6493
Advantage
58
SK Energy and Chemical, Inc.
Tel
--
Fax
--
Email
info@skechem.com
Country
United States
ProdList
78
Advantage
50
Anvia Chemicals, LLC
Tel
--
Fax
--
Email
sales@anviachem.com
Country
United States
ProdList
3933
Advantage
0
Chemcia Scientific, LLC
Tel
--
Fax
--
Email
sales@chemcia.com
Country
United States
ProdList
1412
Advantage
0
Small Molecules, Inc.
Tel
--
Fax
--
Email
sales@small-molecules.com
Country
United States
ProdList
990
Advantage
50
Louston International
Tel
--
Fax
--
Email
sales@louston.com
Country
United States
ProdList
525
Advantage
58
HBCChem Inc.
Tel
--
Fax
--
Email
sales@hbcchem-inc.com
Country
United States
ProdList
4569
Advantage
30
NetQem
Tel
--
Fax
--
Email
sales@netqem.us
Country
United States
ProdList
1641
Advantage
38
Medical Isotopes
Tel
--
Fax
--
Email
stohler@medicalisotopes.com
Country
United States
ProdList
6181
Advantage
68
AstaTech, Inc
Tel
--
Fax
--
Email
sales@astatechinc.com
Country
United States
ProdList
6371
Advantage
58
Waterstone Technology, LLC
Tel
--
Fax
--
Email
sales@waterstonetech.com
Country
United States
ProdList
6786
Advantage
30
AK Scientific, Inc.
Tel
--
Fax
--
Email
sales@aksci.com
Country
United States
ProdList
6347
Advantage
65
Spectrum Chemicals & Laboratory Products
Tel
--
Fax
--
Email
sales@spectrumchemical.com
Country
United States
ProdList
6699
Advantage
77
HONEST JOY HOLDINGS LIMITED
Tel
--
Fax
--
Email
sales@honestjoy.cn
Country
United States
ProdList
6675
Advantage
54
APAC Pharmaceutical, LLC
Tel
--
Fax
--
Email
sales@apacpharma.com
Country
United States
ProdList
6322
Advantage
38
Sciencelab.com, Inc.
Tel
--
Fax
--
Email
accounting@sciencelab.com
Country
United States
ProdList
4159
Advantage
82
ChemContract Research Inc.
Tel
--
Fax
--
Country
United States
ProdList
1526
Advantage
38
Asymchem Laboratories, Inc.
Tel
--
Fax
--
Email
info@asymchem.com
Country
United States
ProdList
1315
Advantage
69
ChemPacific Corporation
Tel
--
Fax
--
Email
sales@chempacific.com
Country
United States
ProdList
6891
Advantage
51
More
Less

View Lastest Price from (S)-(+)-3-Hydroxytetrahydrofuran manufacturers

WUHAN FORTUNA CHEMICAL CO., LTD
Product
(S)-(+)-3-Hydroxytetrahydrofuran 86087-23-2
Price
US $0.00/KG
Min. Order
1KG
Purity
99% GC
Supply Ability
100kg
Release date
2021-08-11
Nanjing Fred Technology Co., Ltd
Product
(s)-(+)-3-hydroxytetrahydrofuran 86087-23-2
Price
US $0.00-0.00/kg
Min. Order
1kg
Purity
98%
Supply Ability
1 ton
Release date
2023-12-20
Suzhou Nordica Biopharma CO.,LTD
Product
(S)-(+)-3-Hydroxytetrahydrofuran 86087-23-2
Price
US $0.00-0.00/kg
Min. Order
1kg
Purity
0.99
Supply Ability
10 tons
Release date
2024-11-14

86087-23-2, (S)-(+)-3-HydroxytetrahydrofuranRelated Search:


  • (S)-TETRAHYDROFURAN-3-OL
  • (S)-(+)-TETRAHYDRO-3-FURANOL
  • (S)-(+)-3-HYDROXY TETAHYDRO FURAN
  • (S)-(-)-3-HYDROXY TETRAHYDRO FURAN
  • (3S)-oxolan-3-ol
  • (2S)-1,4-Epoxy-2-hydroxybutane, (3S)-Tetrahydrofuran-3-ol, (3S)-Oxolan-3-ol
  • Afatinib intermediate B
  • (S)-(+)-3-Hydroxytetrahydrofuran, ee: 95%
  • Afatinib intermediate
  • (S)-(+)-3-HydroxytetrahydrofuranZ
  • (S)-(+)-3-Hydroxytetrahydrofuran 99%
  • (S)-(+)-3-Hydroxytetrahydrofuran, 98% colorless liquid
  • (S)-(+)-3-Hydroxytetrahydrofuran, 98%, ee: 95%
  • (S)-(+)-3-HYDROXYTETRAHYDROFURAN
  • (S)-3-HYDROXYTETRAHYDROFURAN
  • (S)-(+)-3-HYDROXYTETRAHYDROFURANE
  • 3-FURANOL, TETRAHYDRO-, (S)
  • (S)-(+)-3-HYDROXYTETRAHYDROFURAN, 99% (9
  • S-(+)-3-HYDROXYTETRAHYDROFURAN 98+%
  • (S)-(+)-3-HYDOXY TETAHYDRO TETRAHYDRO FURAN
  • (S)-3-Hydroxyterthydrofurane
  • S-HYDROXYTETRAHYDROFURAN
  • S-(+)-3-Hydroxytetrahydofuran
  • (3S)-Tetrahydrofuran-3-ol
  • (3S)-Tetrahydrofuran-3β-ol
  • Oxolane-3β-ol
  • (S)-(+)-3-Hydroxytetrahydrofuran,99%
  • (S)-(+)-tetrahyro-3-furanol
  • (S)-(+)-3-Hydroxytetrahydrofuran ,98% [ee:95%]
  • (2S)-2-Hydroxy-1,4-epoxybutane
  • (3S)-3-Hydroxytetrahydrofuran
  • (3S)-(+)-3-Hydroxytetrahydrofuran 97+%
  • (S)-(+)-3-HYDROXYTETRAHYDROFURAN, (9
  • (S)-(+)-3-Hydroxy-1,2,3,4-tetrahydrofuran
  • S-3-hydroxytetrahydrofur
  • (S)-3-hydroxytetyrahydrofurane
  • S-3- Hydroxytetrafuran
  • 3-Furanol, tetrahydro-, (3S)-
  • (S)-(+)-3-HYDROXYTETRAHYDROFURAN (CAS NO.86087-23-2)
  • (S)-Hydroxy THF
  • (3S)-Tetrahydrofuran-3-ol,(3S)-Oxolan-3-ol
  • (+)-3-Hydroxy-1,2,3,4-Tetrahydrofuran
  • Empagliflozin Impurity 100
  • (S)-3-hydroxytetyrahydrofuran
  • (+)-3-Hydroxytetrahydrofuran
  • 2,4-Dichlorobenzyl Alcohol Impurity 10
  • 86087-23-2
  • 86087-23-3
  • ALCOHOL
  • Simple Alcohols (Chiral)
  • Chiral Building Blocks
  • Heterocyclic Building Blocks
  • Furans
  • Asymmetric Synthesis
  • Afatinib intermediate
  • Chiral Building Blocks
  • Simple Alcohols (Chiral)
  • Synthetic Organic Chemistry