ChemicalBook > Product Catalog >Organic Chemistry >Carboxylic acids and derivatives >Ethyl 5-bromothiophene-3-carboxylate

Ethyl 5-bromothiophene-3-carboxylate

Ethyl 5-bromothiophene-3-carboxylate Structure
CAS No.
170355-38-1
Chemical Name:
Ethyl 5-bromothiophene-3-carboxylate
Synonyms
Ethyl 5-bromothiophene-4-carboxylate;Ethyl 5-bromothiophene-3-carboxylate;Ethyl 5-bromothiophene-3-carboxylate 97+%;5-bromo-3-Thiophenecarboxylic acid ethyl...;PI-35048 ethyl 5-bromothiophene-3-carboxylate;5-bromo-3-Thiophenecarboxylic acid ethyl ester;5-BroMo-thiophene-3-carboxylic acid ethyl ester;3-Thiophenecarboxylic acid, 5-bromo-, ethyl ester;5-Bromothiophene-3-carboxylic acid ethyl ester, >=98%;5-bromo-3-Thiophenecarboxylic acid ethyl ester (9CI ACI)
CBNumber:
CB62514598
Molecular Formula:
C7H7BrO2S
Molecular Weight:
235.1
MOL File:
170355-38-1.mol
MSDS File:
SDS
Modify Date:
2024/3/7 10:46:57

Ethyl 5-bromothiophene-3-carboxylate Properties

Boiling point 65-66 °C
Density 1.572±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
form liquid
color Colourless to yellow
InChI InChI=1S/C7H7BrO2S/c1-2-10-7(9)5-3-6(8)11-4-5/h3-4H,2H2,1H3
InChIKey LUYMKCLOYODOEI-UHFFFAOYSA-N
SMILES C1SC(Br)=CC=1C(OCC)=O

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319
Precautionary statements  P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330
HS Code  2934999090

Ethyl 5-bromothiophene-3-carboxylate Chemical Properties,Uses,Production

Synthesis

20 g (147 mmol) of aluminum chloride are added portion-wise to a solution of 10 g (67 mmol) of ethyl thiophene-3-carboxylate in 160 ml of dichloro-methane, cooled to 0oC. The reaction medium is warmed to room temperature, and a solution of 4 ml (73 mmol) of bromine in 10 ml of dichloromethane is added. After reaction for 50 minutes at room temperature, the reaction medium is poured into a water + ice mixture and extracted with dichloromethane. The organic phase is dried over magnesium sulfate, filtered, and evaporated under vacuum. The residue obtained is purified by chromatography on a column of silica eluted with a 9/1 HEPTANE/ETHYL acetate mixture. 9 g (57percent) of ethyl 5-bromothiophene-3-carboxylate are obtained.

Uses

Ethyl 5-bromothiophene-3-carboxylate is an important organic reagent that can be used as a building block for the synthesis of many organic compounds. After hydrolysis, it can synthesize 5-Bromothiophene-3-carboxylic acid.

Ethyl 5-bromothiophene-3-carboxylate Preparation Products And Raw materials

Raw materials

Preparation Products

Ethyl 5-bromothiophene-3-carboxylate Suppliers

Global( 86)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
A.J Chemicals 91-9810153283 New Delhi, India 6124 58 Inquiry
Shanxi Tihondan Pharmaceutical Technology Co., Ltd +8618235132063 China 3725 58 Inquiry
CONIER CHEM AND PHARMA LIMITED +8618523575427 China 49391 58 Inquiry
career henan chemical co +86-0371-86658258 +8613203830695 China 29826 58 Inquiry
Finetech Industry Limited +86-27-87465837 +8618971612321 China 9624 58 Inquiry
Huida Pharmaceutical Technology (Shanghai) Co., Ltd. +8613601750004 China 439 58 Inquiry
Henan Allgreen Chemical Co.,LTD +86-37155567971 +86-13633837469 China 5986 58 Inquiry
Henan Fengda Chemical Co., Ltd +86-371-86557731 +86-13613820652 China 20308 58 Inquiry
Shanghai Acmec Biochemical Technology Co., Ltd. +undefined18621343501 China 33350 58 Inquiry
Nanjing Bicbiotechnology Co., Ltd +86-2552131256 +86-18251840740 China 6000 58 Inquiry

Ethyl 5-bromothiophene-3-carboxylate Spectrum

Ethyl 5-bromothiophene-3-carboxylate 5-BroMo-thiophene-3-carboxylic acid ethyl ester 5-Bromothiophene-3-carboxylic acid ethyl ester, >=98% 5-bromo-3-Thiophenecarboxylic acid ethyl ester PI-35048 ethyl 5-bromothiophene-3-carboxylate Ethyl 5-bromothiophene-3-carboxylate 97+% 3-Thiophenecarboxylic acid, 5-bromo-, ethyl ester Ethyl 5-bromothiophene-4-carboxylate 5-bromo-3-Thiophenecarboxylic acid ethyl... 3-Thiophenecarboxylic acid, 5-bromo-, ethyl ester (9CI, ACI) 5-bromo-3-Thiophenecarboxylic acid ethyl ester (9CI ACI) 170355-38-1