ethyl 3-(3-fluorophenyl)-5-methylisoxazole-4-carboxylate

Base Information

Chemical Name:ethyl 3-(3-fluorophenyl)-5-methylisoxazole-4-carboxylate
CAS No.:917388-62-6
Molecular Formula:C₁₃H₁₂FNO₃
Molecular Weight:249.242
Hs Code.:
Mol file:917388-62-6.mol

Synonyms:3-(3-fluoro-phenyl)-5-methyl-isoxazole-4-carboxylic acid ethyl ester

Suppliers and Price of ethyl 3-(3-fluorophenyl)-5-methylisoxazole-4-carboxylate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Crysdot
Ethyl3-(3-fluorophenyl)-5-methylisoxazole-4-carboxylate 97%
1g
$ 428.00

American Custom Chemicals Corporation
ETHYL-3-(3-FLUOROPHENYL)-5-METHYLISOXAZOLE-4-CARBOXYLATE 95.00%
5MG
$ 501.25

Total 3 raw suppliers

Chemical Property of ethyl 3-(3-fluorophenyl)-5-methylisoxazole-4-carboxylate

Chemical Property:

Purity/Quality:

99% ^*data from raw suppliers

Ethyl3-(3-fluorophenyl)-5-methylisoxazole-4-carboxylate 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of ethyl 3-(3-fluorophenyl)-5-methylisoxazole-4-carboxylate

There total 4 articles about ethyl 3-(3-fluorophenyl)-5-methylisoxazole-4-carboxylate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 39.0%

: 4341-76-8
Ethyl 2-butynoate

: 58606-42-1
N-hydroxy-3-fluoro-benzenecarboximidoyl chloride

: 917388-62-6
3-(3-fluoro-phenyl)-5-methyl-isoxazole-4-carboxylic acid ethyl ester

Guidance literature:: With triethylamine; In diethyl ether; at 0 - 20 ℃;

Reference yield: 39.0%

: 4341-76-8
Ethyl 2-butynoate

: (Z)-N-hydroxy-3-fluoro-benzenecarboximidoyl chloride

: 917388-62-6
3-(3-fluoro-phenyl)-5-methyl-isoxazole-4-carboxylic acid ethyl ester

Guidance literature:: With triethylamine; In diethyl ether;

Reference yield:

: 456-48-4
3-Fluorobenzaldehyde

: 917388-62-6
3-(3-fluoro-phenyl)-5-methyl-isoxazole-4-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydroxide; hydroxylamine hydrochloride / ethanol; water / -8 - 20 °C

2: N-chloro-succinimide / N,N-dimethyl-formamide / 2 h / 20 - 35 °C

3: triethylamine / diethyl ether / 0 - 20 °C

With N-chloro-succinimide; hydroxylamine hydrochloride; triethylamine; sodium hydroxide; In diethyl ether; ethanol; water; N,N-dimethyl-formamide;