1H-Indole-1-carboxylic acid, 7-(bromomethyl)-, 1,1-dimethylethyl ester

Base Information

Chemical Name:1H-Indole-1-carboxylic acid, 7-(bromomethyl)-, 1,1-dimethylethyl ester
CAS No.:442910-45-4
Molecular Formula:C₁₄H₁₆BrNO₂
Molecular Weight:310.191
Hs Code.:2933990090
Mol file:442910-45-4.mol

Synonyms:1H-Indole-1-carboxylic acid, 7-(broMoMethyl)-, 1,1-diMethylethyl ester

Suppliers and Price of 1H-Indole-1-carboxylic acid, 7-(bromomethyl)-, 1,1-dimethylethyl ester

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
tert-Butyl7-(bromomethyl)-1H-indole-1-carboxylate 95+%
250mg
$ 625.00

Chemenu
tert-Butyl7-(bromomethyl)-1H-indole-1-carboxylate 95%
1g
$ 729.00

American Custom Chemicals Corporation
TERT-BUTYL-7-(BROMOMETHYL)-1H-INDOLE-1-CARBOXYLATE 95.00%
5MG
$ 495.72

Alichem
tert-Butyl7-(bromomethyl)-1H-indole-1-carboxylate
1g
$ 621.72

Total 12 raw suppliers

Chemical Property of 1H-Indole-1-carboxylic acid, 7-(bromomethyl)-, 1,1-dimethylethyl ester

Chemical Property:

PSA：31.23000
LogP:4.31940
Storage Temp.:2-8°C

Purity/Quality:

97% ^*data from raw suppliers

tert-Butyl7-(bromomethyl)-1H-indole-1-carboxylate 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 1H-Indole-1-carboxylic acid, 7-(bromomethyl)-, 1,1-dimethylethyl ester

There total 6 articles about 1H-Indole-1-carboxylic acid, 7-(bromomethyl)-, 1,1-dimethylethyl ester 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: 94.0%

: 24424-99-5
di-tert-butyl dicarbonate

: 15936-71-7
ethyl 5-chloro-7-methyl-1H-indole-2-carboxylate

: 442910-45-4
tert-butyl 7-(bromomethyl)-1H-indole-1-carboxylate

Guidance literature:: With dmap; triethylamine; In dichloromethane;

Reference yield: 89.0%

: 442910-62-5
7-methylindole-1-carboxylic acid tert-butyl ester

: 442910-45-4
tert-butyl 7-(bromomethyl)-1H-indole-1-carboxylate

Guidance literature:: With N-Bromosuccinimide; benzoic peroxyanhydride; In tetrachloromethane; at 80 ℃; for 2h; Concentration; Temperature;

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 442910-45-4
tert-butyl 7-(bromomethyl)-1H-indole-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine; dmap / dichloromethane / 2 h / 20 °C

2: N-Bromosuccinimide; benzoic peroxyanhydride / tetrachloromethane / 2 h / 80 °C

With dmap; N-Bromosuccinimide; triethylamine; benzoic peroxyanhydride; In tetrachloromethane; dichloromethane;