ChemicalBook > CAS DataBase List > ETHYL (S)-3,4-EPOXYBUTANOATE

ETHYL (S)-3,4-EPOXYBUTANOATE

Product Name
ETHYL (S)-3,4-EPOXYBUTANOATE
CAS No.
112083-63-3
Chemical Name
ETHYL (S)-3,4-EPOXYBUTANOATE
Synonyms
TB-1983;Brivanib Impurity 1;ETHYL-(S)-OXIRANE ACETATE;ethyl()-2-0xiranylacetate;Levocarnitine Impurity 46;ETHYL (S)-OXIRANE-2-ACETATE;ETHYL (S)-2-OXIRANYLACETATE;ETHYL (S)-3,4-EPOXYBUTYRATE;ETHYL (S)-3,4-EPOXYBUTANOATE;ETHYL (3S)-3,4-EPOXYBUTYRATE
CBNumber
CB4282413
Molecular Formula
C6H10O3
Formula Weight
130.14
MOL File
112083-63-3.mol
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ETHYL (S)-3,4-EPOXYBUTANOATE Property

Boiling point:
158.3±13.0 °C(Predicted)
Density 
1.099±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
Water Solubility 
Decomposes in water.
Sensitive 
Air Sensitive
CAS DataBase Reference
112083-63-3(CAS DataBase Reference)
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Safety

Hazard Codes 
Xn
Risk Statements 
20/21/22-36/37/38
Safety Statements 
26-36/37
WGK Germany 
3
10-23
HS Code 
2932990090
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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.

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

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

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

P405Store locked up.

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N-Bromosuccinimide Price

Alfa Aesar
Product number
H27891
Product name
Ethyl (S)-2-oxiranylacetate, 97%
Packaging
500mg
Price
$177
Updated
2021/12/16
Apolloscientific
Product number
OR4600
Product name
Ethyl (S)-3,4-epoxybutanoate
Purity
97%
Packaging
500mg
Price
$203
Updated
2021/12/16
SynQuest Laboratories
Product number
2123-1-S1
Product name
Ethyl (S)-3,4-epoxybutanoate
Purity
97%
Packaging
500mg
Price
$240
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
CHM0029443
Product name
ETHYL (S)-3,4-EPOXYBUTANOATE
Purity
95.00%
Packaging
500MG
Price
$817.39
Updated
2021/12/16
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ETHYL (S)-3,4-EPOXYBUTANOATE Chemical Properties,Usage,Production

Uses

Mainly employed inorganic synthesis. They are starting materials for the condensation reactions. Homoallylic alcohol is readily available from the regiospecific ring opening of commercially available ethyl (S)-oxiranyl acetate with the cuprate derived from vinylmagnesium bromide and copper bromide-dimethyl sulfide complex in 88 % yield.

Hazard

Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation.

storage

Air Sensitive. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents, excess heat, air. Store at 2-8°C.

ETHYL (S)-3,4-EPOXYBUTANOATE Preparation Products And Raw materials

Raw materials

Preparation Products

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ETHYL (S)-3,4-EPOXYBUTANOATE Suppliers

Fischer Chemicals AG
Tel
--
Fax
--
Email
contact@fischer-group.ch
Country
Switzerland
ProdList
411
Advantage
58
SIGMA-RBI
Tel
--
Fax
--
Country
Switzerland
ProdList
6896
Advantage
91

112083-63-3, ETHYL (S)-3,4-EPOXYBUTANOATERelated Search:


  • 2-Oxiraneacetic acid,ethyl ester, (2S)-
  • Ethyl (S)-2-(oxiran-2-yl)acetate
  • Ethyl (S)-3,4-epoxybutanoate 97%
  • OXIRANEACETIC ACID, ETHYL ESTER, (S)
  • ETHYL (S)-OXIRANE-2-ACETATE
  • ETHYL-(S)-OXIRANE ACETATE
  • ETHYL (3S)-3,4-EPOXYBUTYRATE
  • ETHYL (S)-3,4-EPOXYBUTANOATE
  • ETHYL (S)-(-)-3,4-EPOXYBUTYRATE
  • ETHYL (S)-3,4-EPOXYBUTYRATE
  • ETHYL (S)-2-OXIRANYLACETATE
  • (S)-Ethyl 2-(oxiran-2-yl)acetate
  • ethyl()-2-0xiranylacetate
  • (S)-1-Boc-2-pyrrolidinonitrile
  • (S)-2-Cyanopyrrolidine, N-BOC protected
  • Ethyl (S)-3,4-epoxybutyrate, Ethyl (S)-oxirane-2-acetate
  • Ethyl (S)-2-oxiraneacetate, 97%
  • ethyl 2-[(2S)-oxiran-2-yl]acetate
  • Levocarnitine Impurity 46
  • Ethyl (S)-2-oxiranylacetate, 97%,
  • TB-1983
  • Brivanib Impurity 1
  • 112083-63-3
  • Organic Building Blocks
  • Epoxides
  • Asymmetric Synthesis
  • Chiral Building Blocks
  • Chiral Compounds
  • Epoxides
  • Heterocycles