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(2S)-(+)-Glycidyl tosylate

Product Name
(2S)-(+)-Glycidyl tosylate
CAS No.
70987-78-9
Chemical Name
(2S)-(+)-Glycidyl tosylate
Synonyms
(S)-GLYCIDYL TOSYLATE;(S)-Glycidyl;(+)-glycidyltosylate;(2S)-(+)-Glycidyl to;(S)-Glycidil Tosylate;(S)-(+)-GLYCIDYL TOSYLATE;(2S)-(+)-Lucidly tosylate;(2S)-(+)-GLYCIDYL TOSYLATE;Levodropropizine Impurity 38;(S)-Glycidyl Tosylate,99%e.e.
CBNumber
CB8494744
Molecular Formula
C10H12O4S
Formula Weight
228.26
MOL File
70987-78-9.mol
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(2S)-(+)-Glycidyl tosylate Property

Melting point:
46-49 °C(lit.)
alpha 
17 º (c=2.5, CHCl3)
Boiling point:
340.07°C (rough estimate)
Density 
1.3749 (rough estimate)
refractive index 
1.5400 (estimate)
Flash point:
>230 °F
storage temp. 
2-8°C
solubility 
Dioxane (Slightly), DMSO (Slightly), Methanol (Slightly)
form 
Fluffy Powder
color 
White
Water Solubility 
decomposes
BRN 
3592143
CAS DataBase Reference
70987-78-9(CAS DataBase Reference)
NIST Chemistry Reference
(2S)-glycidyl tosylate(70987-78-9)
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Safety

Hazard Codes 
T,N,Xi
Risk Statements 
45-41-43-51/53-68
Safety Statements 
53-45-61
RIDADR 
UN 3077 9/PG 3
WGK Germany 
3
RTECS 
RR0510050
F 
3-10-21
HazardClass 
9
PackingGroup 
III
HS Code 
29109000
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H317May cause an allergic skin reaction

H318Causes serious eye damage

H341Suspected of causing genetic defects

H350May cause cancer

H411Toxic to aquatic life with long lasting effects

Precautionary statements

P201Obtain special instructions before use.

P273Avoid release to the environment.

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

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

P308+P313IF exposed or concerned: Get medical advice/attention.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
540129
Product name
(2S)-(+)-Glycidyl tosylate
Purity
98%
Packaging
5g
Price
$37.5
Updated
2024/03/01
Sigma-Aldrich
Product number
540129
Product name
(2S)-(+)-Glycidyl tosylate
Purity
98%
Packaging
25g
Price
$124
Updated
2023/06/20
TCI Chemical
Product number
T1612
Product name
(2S)-(+)-Glycidyl p-Toluenesulfonate
Purity
>98.0%(GC)
Packaging
5g
Price
$62
Updated
2024/03/01
TCI Chemical
Product number
T1612
Product name
(2S)-(+)-Glycidyl p-Toluenesulfonate
Purity
>98.0%(GC)
Packaging
25g
Price
$182
Updated
2024/03/01
Alfa Aesar
Product number
H56000
Product name
(2S)-(+)-Glycidyl p-toluenesulfonate, 99%
Packaging
1g
Price
$28.9
Updated
2021/12/16
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(2S)-(+)-Glycidyl tosylate Chemical Properties,Usage,Production

Chemical Properties

white to light yellow crystal powde

Uses

Used in the first enantioselective synthesis of (R)- and (S)-4-acetyl-3-(hydroxymethyl)-3,4-dihydro-2H-pyrido[3,2-b]oxazines.

Uses

(2S)-(+)-Glycidyl tosylate is protected Glycidol, used as an intermediate in the preparation of neurochemicals.

(2S)-(+)-Glycidyl tosylate Preparation Products And Raw materials

Raw materials

Preparation Products

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(2S)-(+)-Glycidyl tosylate Suppliers

Belgium 3 Canada 2 China 136 Europe 4 France 1 Germany 4 India 6 Japan 8 Slovakia 1 South Korea 2 Switzerland 1 United Kingdom 12 United States 41 Global 221
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Europe
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ecochem international chemical broker
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Camida
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Europe
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View Lastest Price from (2S)-(+)-Glycidyl tosylate manufacturers

Hebei Weibang Biotechnology Co., Ltd
Product
(2S)-(+)-Glycidyl tosylate 70987-78-9
Price
US $0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
500000kg
Release date
2024-10-30
Hebei Mojin Biotechnology Co., Ltd
Product
(2S)-(+)-Glycidyl tosylate 70987-78-9
Price
US $0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
50000KG/month
Release date
2023-10-24
Career Henan Chemical Co
Product
(2S)-(+)-Glycidyl tosylate 70987-78-9
Price
US $1.00/KG
Min. Order
1KG
Purity
98%
Supply Ability
1kg,5kg,100kg
Release date
2019-07-04

70987-78-9, (2S)-(+)-Glycidyl tosylateRelated Search:

ETHYLENE OXIDE Methanol Sodium p-toluenesulfonate 4-CHLOROBENZOYLACETONITRILE Sorafenib tosylate Sodium xylenesulfonate Glycidyl acrylate p-Toluenesulfonic acid 1,2-EPOXYTETRADECANE (R)-(+)-Glycidol PROPYL P-TOLUENESULFONATE (S)-Oxiranemethanol (2R)-(-)-Glycidyl tosylate (S)-(+)-2-HYDROXYPROPYL P-TOLUENESULFONATE 1,6:3,4-DIANHYDRO-2-O-TOSYL-BETA-D-GALACTOPYRANOSE GLYCIDYL 4-TOLUENESULFONATE R(-)or S(+) glycidyl tosylate (2S)-(+)-Glycidyl tosylate

  • (2S)-Oxiran-2-ylmethyl 4-methylbenzenesulphonate 98%
  • (S)-Glycidyl Tosylate,99%e.e.
  • 2-Oxiranylmethyl 4-methylbenzenesulfonate
  • 4-methylbenzenesulfonate,(s)-oxiranemethano
  • (S)-Oxiran-2-ylMethyl 4-Methylbenzenesulfonate
  • (2S)-2-OxiraneMethanol 2-(4-Methylbenzenesulfonate)
  • (S)-(2,3-Epoxypropan-1-yl) 4-Methylbenzenesulfonate
  • (S)-Oxiran-2-ylMethyl Toluene-4-sulfonate
  • (S)-Toluene-4-sulfonic Scid OxiranylMethyl Ester
  • (2S)-(+)-Glycidyl Tosylate p-Toluenesulfonic Acid (2S)-(+)-Glycidyl Ester
  • (S)-Glycidil Tosylate
  • (S)-Glycidyl toluene-4-sulphonate
  • (+)-glycidyltosylate
  • (S)-(+)-Oxirane-2-methanol-4-toluenesulfonate
  • (2S)-(+)-Glycidyl tosylate, 99+%
  • (S)-Glycidyl
  • (S)-glycidyl toluene-4-sulfonate
  • (2S)-(+)-GLYCIDYL TOSYLATE ((S)-(+)-OXIRANE-2-METHANOL)
  • oxiranemethanol, 4-methylbenzene-sulfonate, (S)-
  • (S)-(+)-Glycidyl p-toluenesulfonate, (S)-(+)-Oxirane-2-methanol p-toluenesulfonate
  • (2S)-(+)-Glycidyl tosylate ,98%
  • (2S)-(+)-Glycidyl to
  • (2S)-(+)-GLYCIDYL P-TOLUENESULFONATE
  • (2S)-GLYCIDYL TOLUENESULFONATE
  • (2S)-(+)-GLYCIDYL TOSYLATE
  • 2-(S)-OXIRAN-2-YLMETHYL-4-METHYL BENZENE SULPHONATE
  • P-TOLUENESULFONIC ACID (2S)-(+)-GLYCIDYL ESTER
  • (S)-(+)-OXIRANE-2-METHANOL P-TOLUENESULFONATE
  • (S)-OXIRANE-2-METHANOL P-TOLUENESULFONATE
  • S(+)-OXIRANE-2-METHANOL TOLUENE-4-SULFONATE
  • (S)-(+)-GLYCIDYL P-TOLUENESULFONATE
  • (S)-(+)-GLYCIDYL TOSYLATE
  • (S)-GLYCIDYL TOSYLATE
  • (S)-2,3-EPOXY-1-PROPYL P-TOLUENESULFONATE
  • OXIRANEMETHANOL, 4-METHYLBENZENESULFONATE, (2S)-
  • (2S)-(+)-Glycidyl tosylate, 98.5%
  • 2-Oxiranemethanol, 2-(4-methylbenzenesulfonate), (2S)-
  • (2S)-(+)-Lucidly tosylate
  • Levodropropizine Impurity 38
  • 70987-78-9
  • C10H12O4S
  • C10H12O4S1
  • Chiral Building Blocks
  • Epoxides
  • Organic Building Blocks
  • Asymmetric Synthesis
  • Carbohydrates & Derivatives
  • Sulfur & Selenium Compounds
  • Phenyls & Phenyl-Het
  • chiral
  • CHIRAL COMPOUNDS
  • Aromatics
  • Chiral Compound
  • Phenyls & Phenyl-Het