1H-Indole-3-carboxaldehyde, 4-bromo-1-methyl-

Base Information

Chemical Name:1H-Indole-3-carboxaldehyde, 4-bromo-1-methyl-
CAS No.:338760-45-5
Molecular Formula:C10H8BrNO
Molecular Weight:238.084
Hs Code.:
Mol file:338760-45-5.mol

Synonyms:4-bromo-1-methyl-indole-3-carboxaldehyde;4-Bromo-1-methyl-1H-indole-3-carbaldehyde;

Suppliers and Price of 1H-Indole-3-carboxaldehyde, 4-bromo-1-methyl-

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

Labseeker
1H-Indole-3-carboxaldehyde,4-bromo-1-methyl- 95
10g
$ 2292.00

Crysdot
4-Bromo-1-methyl-1H-indole-3-carbaldehyde 95+%
1g
$ 772.00

Chemenu
4-bromo-1-methyl-1H-indole-3-carbaldehyde 95%
1g
$ 729.00

American Custom Chemicals Corporation
4-BROMO-1-METHYL-1H-INDOLE-3-CARBALDEHYDE 95.00%
5MG
$ 501.51

Total 3 raw suppliers

Chemical Property of 1H-Indole-3-carboxaldehyde, 4-bromo-1-methyl-

Chemical Property:

PSA：22.00000
LogP:2.75330
Storage Temp.:2-8°C

Purity/Quality:

95+% ^*data from raw suppliers

1H-Indole-3-carboxaldehyde,4-bromo-1-methyl- 95 ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses 4-Bromo-1-methyl-1H-indole-3-carbaldehyde is used in preparation of 3-substituted 1H-indoles and 1H-pyrrolopyridines as mTOR kinase and PI3 kinase inhibitors.

Technology Process of 1H-Indole-3-carboxaldehyde, 4-bromo-1-methyl-

There total 4 articles about 1H-Indole-3-carboxaldehyde, 4-bromo-1-methyl- 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: 88.0%

: 98600-34-1
4-bromo-1H-indole-3-carbaldehyde

: 74-88-4
methyl iodide

: 338760-45-5
4-bromo-1-methyl-1H-indole-3-carbaldehyde

Guidance literature:: 4-bromo-1H-indole-3-carbaldehyde; With sodium hydride; In N,N-dimethyl-formamide; at 0 ℃;

methyl iodide; In N,N-dimethyl-formamide; at 20 ℃;