Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Thiophene compounds >  ETHYL 5-CHLOROTHIOPHENE-2-CARBOXYLATE

ETHYL 5-CHLOROTHIOPHENE-2-CARBOXYLATE

Basic information Safety Supplier Related

ETHYL 5-CHLOROTHIOPHENE-2-CARBOXYLATE Basic information

Product Name:
ETHYL 5-CHLOROTHIOPHENE-2-CARBOXYLATE
Synonyms:
  • RARECHEM AL BI 0303
  • Ethyl 5-chloro-2-thiophenecarboxylate
  • 5-Chlorothiophene-2-carboxylic acid ethyl ester
  • Ethyl 5-chlorothiophene-2-carboxlate
  • Ethyl 5-chlorothiophene-2-carboxylate, 98+%
  • 2-Thiophenecarboxylic acid, 5-chloro-, ethyl ester
  • 2- chlorinethiophene -5-ethyl forMate
  • Rivaroxaban impurity P2-O
CAS:
5751-82-6
MF:
C7H7ClO2S
MW:
190.65
Mol File:
5751-82-6.mol
More
Less

ETHYL 5-CHLOROTHIOPHENE-2-CARBOXYLATE Chemical Properties

Boiling point:
70-71°C 1mm
Density 
1.312±0.06 g/cm3(Predicted)
refractive index 
1.5380
Flash point:
70-71°C/1mm
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
form 
clear liquid
color 
Colorless to Light yellow
BRN 
128707
CAS DataBase Reference
5751-82-6
More
Less

Safety Information

Risk Statements 
36/38
Safety Statements 
26-36-37
HS Code 
29349990

MSDS

  • Language:English Provider:ALFA
More
Less

ETHYL 5-CHLOROTHIOPHENE-2-CARBOXYLATE Usage And Synthesis

Chemical Properties

Colorless to light yellow liquid

Synthesis

24065-33-6

64-17-5

5751-82-6

Concentrated sulfuric acid (15 mL) was slowly added to a stirring solution of 5-chlorothiophene-2-carboxylic acid (15 g, 0.0925 mol) in ethanol (300 mL) at room temperature. The reaction mixture was stirred continuously under anhydrous conditions for 16 hours. Upon completion of the reaction, the reaction mixture was concentrated by distillation under reduced pressure. The concentrate was diluted with ethyl acetate (300 mL) and the organic layer was subsequently washed sequentially with water (3 x 100 mL), saturated sodium bicarbonate solution (3 x 100 mL) and saturated saline (100 mL). The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to give ethyl 5-chlorothiophene-2-carboxylate (14 g, 80% yield) as a colorless liquid.

References

[1] Patent: WO2015/18534, 2015, A1. Location in patent: Page/Page column 39
[2] Journal of the American Chemical Society, 1954, vol. 76, p. 5131
[3] Journal of the American Chemical Society, 1954, vol. 76, p. 5131
[4] Chemistry - A European Journal, 2016, vol. 22, # 1, p. 211 - 221

ETHYL 5-CHLOROTHIOPHENE-2-CARBOXYLATE Preparation Products And Raw materials

Raw materials

ETHYL 5-CHLOROTHIOPHENE-2-CARBOXYLATESupplier

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
PharmaBlock Sciences (Nanjing),Inc.
Tel
025-86918202 4000255188
Email
sales@pharmablock.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Email
market03@meryer.com
future industrial shanghai co., ltd
Tel
400-0066400 13621662912
Email
sales@jonln.com
New Energy Chemicals
Tel
0515-82159099 13770142076
Email
info@njuchem.com