ChemicalBook > CAS DataBase List > Ethyl 1,3-dithiane-2-carboxylate

Ethyl 1,3-dithiane-2-carboxylate

Product Name
Ethyl 1,3-dithiane-2-carboxylate
CAS No.
20462-00-4
Chemical Name
Ethyl 1,3-dithiane-2-carboxylate
Synonyms
Carboethoxy-1,3-dithiane;2-Carboethoxy-1,3-dithiane;2-Ethoxycarbonyl-1,3-dithiane;ETHYL 1,3-DITHIANE-2-CARBOXYLATE;Ethyl1,3-Dithiane-2-carboxylate>Ethyl 1,3-dithiane-2-carboxylate, 98+%;ETHYL-1 3-DITHIANE-2-CARBOXYLATE 99% (&;ETHYL 1,3-DITHIANE-2-CARBOXYLATE FOR SYN;2-(2-phenylimino-3-thiazolidinyl)ethanol;m-Dithiane-2-carboxylic acid, ethyl ester
CBNumber
CB6490333
Molecular Formula
C7H12O2S2
Formula Weight
192.3
MOL File
20462-00-4.mol
More
Less

Ethyl 1,3-dithiane-2-carboxylate Property

Melting point:
19-21°C
Boiling point:
75-77 °C/0.2 mmHg (lit.)
Density 
1.22 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.539(lit.)
Flash point:
130 °F
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
clear liquid
color 
Colorless to Light yellow to Light orange
Water Solubility 
Slightly miscible with water.
BRN 
1424352
InChI
InChI=1S/C7H12O2S2/c1-2-9-6(8)7-10-4-3-5-11-7/h7H,2-5H2,1H3
InChIKey
ANEDZEVDORCLPM-UHFFFAOYSA-N
SMILES
S1CCCSC1C(OCC)=O
CAS DataBase Reference
20462-00-4(CAS DataBase Reference)
NIST Chemistry Reference
Ethyl 1,3-dithiane-2-carboxylate(20462-00-4)
More
Less

Safety

Risk Statements 
10
Safety Statements 
26-36/37/39-45
RIDADR 
UN 3272 3/PG 3
WGK Germany 
3
9-13
HazardClass 
3
PackingGroup 
III
HS Code 
29349990
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H226Flammable liquid and vapour

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P233Keep container tightly closed.

P240Ground/bond container and receiving equipment.

P241Use explosion-proof electrical/ventilating/lighting/…/equipment.

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

P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.

P403+P235Store in a well-ventilated place. Keep cool.

P501Dispose of contents/container to..…

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
43749
Product name
Ethyl 1,3-dithiane-2-carboxylate
Purity
technical, ≥90% (GC)
Packaging
5ml
Price
$296
Updated
2024/03/01
TCI Chemical
Product number
D1648
Product name
Ethyl 1,3-Dithiane-2-carboxylate
Purity
>98.0%(GC)
Packaging
1g
Price
$84
Updated
2024/03/01
TCI Chemical
Product number
D1648
Product name
Ethyl 1,3-Dithiane-2-carboxylate
Purity
>98.0%(GC)
Packaging
5g
Price
$231
Updated
2024/03/01
Alfa Aesar
Product number
L00663
Product name
Ethyl 1,3-dithiane-2-carboxylate, 98+%
Packaging
5g
Price
$93.4
Updated
2024/03/01
Alfa Aesar
Product number
L00663
Product name
Ethyl 1,3-dithiane-2-carboxylate, 98+%
Packaging
25g
Price
$372
Updated
2024/03/01
More
Less

Ethyl 1,3-dithiane-2-carboxylate Chemical Properties,Usage,Production

Chemical Properties

clear yellowish liquid

Uses

Ethyl 1,3-dithiane-2-carboxylate is used in syn-selective aldol reactions. It undergoes asymmetric oxidation to give trans bis-sulfoxide. It is used to generate carbanon, which finds application in the preparation of alfa- keto esters.

Preparation

To a solution of BF3. Et2O (57.5 mL, 0.454 mmol) in CHC13 (180 mL) heated at reflux was added dropwise, over a 1h period, a solution of 1,3-propanedithiol (22.7 mL, 0.227 mmol), followed by ethyl diethoxyacetate (40 g, 0.227 mmol) in CHCl3 (40 mL). The resulting mixture was heated for 30 minutes, and then cooled to rt. The cooled solution was washed 2 times with water, once with saturated aqueous NaHC03, and then re-washed with water. The combined organic phases were dried over MgS04, then evaporated to give 41 g (94%) of Ethyl 1,3-dithiane-2-carboxylate as a yellow oi. Yield: 94%

Application

Ethyl 1,3-dithiane-2-carboxylate is a synthetic compound that is used in the synthesis of organic compounds . It is used in asymmetric synthesis to produce chiral products from achiral starting materials. The desulfurization reaction of ethyl 1,3-dithiane-2-carboxylate produces a mixture of the two possible stereoisomers of the product. This mixture can be separated by phase chromatography and then hydrolyzed to give the desired product. In dyslipidemia, ethyl 1,3-dithiane-2-carboxylate inhibits the activity of hepatic lipase and acidolysis. This inhibition leads to an increase in serum triglycerides and cholesterol levels. This compound also has been shown to have antiplatelet properties when administered orally or intravenously to rats without affecting platelet aggregation rates.

Synthesis Reference(s)

Synthetic Communications, 11, p. 343, 1981 DOI: 10.1080/00397918108063615

General Description

Ethyl 1,3-dithiane-2-carboxylate is an α-keto acid equivalent and bulky equivalent of acetate. It participates in syn-selective aldol reactions. It can be prepared from the reaction of ethyl diethoxyacetate and 1,3-propanedithiol in the presence of BF3/Et2O. Asymmetric oxidation of ethyl 1,3-dithiane-2-carboxylate by Modena protocol has been reported to afford trans bis-sulfoxide in 60% yield. Carbanion from ethyl 1,3-dithiane-2-carboxylate may be employed for the preparation of α-keto esters.

Purification Methods

Dissolve the ester in CHCl3, wash with aqueous K2CO3, twice with H2O, dry over MgSO4, filter, evaporate and distil the residue. [Eliel & Hartman J Org Chem 37 505 1972, Seebach Synthesis 1 17 1969, Beilstein 19/7 V 227.]

Ethyl 1,3-dithiane-2-carboxylate Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Ethyl 1,3-dithiane-2-carboxylate Suppliers

Alchem Pharmtech,Inc.
Tel
8485655694
Email
sales@alchempharmtech.com
Country
United States
ProdList
63687
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
Fluorochem Ltd.
Tel
--
Fax
--
Email
enquiries@fluorochem.co.uk
Country
United States
ProdList
4583
Advantage
58
Alichem Inc.
Tel
--
Fax
--
Email
sales@alichem.com
Country
United States
ProdList
6167
Advantage
58
TCI America, Inc. (Tokyo Chemical Industry Co., Ltd.)
Tel
--
Fax
--
Email
.Crew@tcichemicals.com
Country
United States
ProdList
3164
Advantage
58
OChem Incorporation
Tel
--
Fax
--
Email
sales@ocheminc.com
Country
United States
ProdList
6501
Advantage
60
VWR International, LLC.
Tel
--
Fax
--
Email
@sargentwelch.com
Country
United States
ProdList
6262
Advantage
58
United States Biological
Tel
--
Fax
--
Email
chemicals@usbio.net
Country
United States
ProdList
6214
Advantage
80
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
Matrix Scientific
Tel
--
Fax
--
Email
sales@matrixscientific.com
Country
United States
ProdList
6632
Advantage
80
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6962
Advantage
56
Waterstone Technology, LLC
Tel
--
Fax
--
Email
sales@waterstonetech.com
Country
United States
ProdList
6786
Advantage
30
Alfa Aesar
Tel
--
Fax
--
Email
tech@alfa.com
Country
United States
ProdList
6814
Advantage
81
2A PharmaChem USA
Tel
--
Fax
--
Email
sales@2apharmachem.com
Country
United States
ProdList
6137
Advantage
39
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6718
Advantage
47
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
ChemPacific Corporation
Tel
--
Fax
--
Email
sales@chempacific.com
Country
United States
ProdList
6891
Advantage
51
BOSCHE SCIENTIFIC, LLC
Tel
--
Fax
--
Email
Sales@BoscheSci.com
Country
United States
ProdList
6477
Advantage
55
More
Less

View Lastest Price from Ethyl 1,3-dithiane-2-carboxylate manufacturers

Huida Pharmaceutical Technology (Shanghai) Co., Ltd.
Product
Ethyl 1,3-dithiane-2-carboxylate 20462-00-4
Price
US $0.00-0.00/kg
Min. Order
0.1kg
Purity
98%
Supply Ability
100kg
Release date
2023-03-07
Huida Pharmaceutical Technology (Shanghai) Co., Ltd.
Product
Ethyl 1,3-dithiane-2-carboxylate 20462-00-4
Price
US $0.00-0.00/kg
Min. Order
0.1kg
Purity
98%
Supply Ability
100kg
Release date
2023-03-12
Zhengzhou Gecko Scientific Inc.
Product
Ethyl 1,3-dithiane-2-carboxylate 20462-00-4
Price
US $0.00-0.00/g
Min. Order
10g
Purity
98%
Supply Ability
10kg
Release date
2022-09-29

20462-00-4, Ethyl 1,3-dithiane-2-carboxylateRelated Search:


  • ETHYL-1 3-DITHIANE-2-CARBOXYLATE 99% (&
  • Ethyl 1,3-dithiane-2-carboxylate, 98+%
  • 2-Ethoxycarbonyl-1,3-dithiane
  • Ethyl Glyoxylate Trimethylene Dithioacetal
  • ETHYL 1,3-DITHIANE-2-CARBOXYLATE FOR SYN
  • m-Dithiane-2-carboxylic acid, ethyl ester
  • 2-Carboethoxy-1,3-dithiane
  • Carboethoxy-1,3-dithiane
  • GLYOXYLIC ACID ETHYL ESTER TRIMETHYLENEMERCAPTAL
  • ETHYL 1,3-DITHIANE-2-CARBOXYLATE
  • 1,3-DITHIANE-2-CARBOXYLIC ACID ETHYL ESTER
  • 2-(2-phenylimino-3-thiazolidinyl)ethanol
  • Ethyl1,3-Dithiane-2-carboxylate&gt
  • 20462-00-4
  • C7H12O2S2
  • Others
  • Sulfur Compounds (for Synthesis)
  • Building Blocks
  • Heterocyclic Building Blocks
  • S-Containing
  • Heterocyclic Compounds
  • Sulfur Compounds (for Synthesis)
  • Synthetic Organic Chemistry
  • Sulfur compounds