2-Benzofurancarboxylic acid ethyl ester

2-Benzofurancarboxylic acid ethyl ester Structure
CAS No.
3199-61-9
Chemical Name:
2-Benzofurancarboxylic acid ethyl ester
Synonyms
Ethyl CouMarilate;RARECHEM AL BI 0556;Ethyl 2-benzofurancarboxylate;ethyl benzofuran-2-carboxylate;Ethyl 1-benzofuran-2-carboxylate;Ethyl benzo[b]furan-2-carboxylate;Ethyl benzo[b]furan-2-carboxylate 97%;BENZOFURAN-2-CARBOXLIC ACID ETHYL ESTER;BENZOFURAN-2-CARBOXYLIC ACID ETHYL ESTER;2-BENZOFURANCARBOXYLIC ACID, ETHYL ESTER
CBNumber:
CB4414494
Molecular Formula:
C11H10O3
Molecular Weight:
190.2
MOL File:
3199-61-9.mol
MSDS File:
SDS
Modify Date:
2024/7/9 21:58:15

2-Benzofurancarboxylic acid ethyl ester Properties

Melting point 166-170℃
Boiling point 105°/0.1mm
Density 1.1656
refractive index 1.5640 (estimate)
Flash point >110℃
storage temp. 2-8°C
CAS DataBase Reference 3199-61-9(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302-H319
Precautionary statements  P305+P351+P338
Hazard Codes  T
WGK Germany  3
HazardClass  IRRITANT
HS Code  2932190090

2-Benzofurancarboxylic acid ethyl ester price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 763632 Ethyl benzofuran-2-carboxylate 97% 3199-61-9 1G ₹5693.95 2022-06-14 Buy
Product number Packaging Price Buy
763632 1G ₹5693.95 Buy

2-Benzofurancarboxylic acid ethyl ester Chemical Properties,Uses,Production

Uses

Ethyl Coumarilate has been used as a reactant for the preparation of benzofuropyridines that have a high affinity for the α2-adrenoceptor.

Preparation

Synthesis of ethyl benzofuran-2-carboxylate: Salicylaldehyde (20.0 mL, 0.164 mol) and diethyl bromomalonate (40.0 mL, 0.168 mol) in ethyl methyl ketone (40.0 mL, 0.555 mol) was treated with anhydrous potassium carbonate (20.0 g,0.869 mol). The reaction mixture was refluxed for 18 h on steam bath. Ethyl methyl ketone was distilled off under reduced pressure and the residue formed was dissolved in 400 mL of water and cooled in an ice-bath. It was acidified with dil H2SO4. The product formed was extracted with 25 mL portion of solvent ether twice and the extract was washed with sodium bicarbonate solution. It was dried over calcium chloride. Solvent was removed and the residue ethyl benzofuran-2-carboxylate was dried.

Synthesis Reference(s)

Tetrahedron Letters, 27, p. 6315, 1986 DOI: 10.1016/S0040-4039(00)87796-5

2-Benzofurancarboxylic acid ethyl ester Preparation Products And Raw materials

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BENZOFURAN-2-CARBOXYLIC ACID ETHYL ESTER BENZOFURAN-2-CARBOXLIC ACID ETHYL ESTER Ethyl benzo[b]furan-2-carboxylate 97% RARECHEM AL BI 0556 2-BENZOFURANCARBOXYLIC ACID, ETHYL ESTER ethyl benzofuran-2-carboxylate Ethyl 2-benzofurancarboxylate 2-(Ethoxycarbonyl)benzo[b]furan, Ethyl 1-benzofuran-2-carboxylate Ethyl CouMarilate Ethyl 1-benzofuran-2-carboxylate 1-isobenzofurancarboxylic acid ethyl ester Ethyl benzo[b]furan-2-carboxylate 3199-61-9 Miscellaneous