1H-Indole-5-carboxylic acid

Base Information

Chemical Name:1H-Indole-5-carboxylic acid
CAS No.:142396-03-0
Molecular Formula:C9H7NO2
Molecular Weight:161.15738
Hs Code.:
Mol file:142396-03-0.mol

Synonyms:1H-Indole-5-carboxylic acid, radical ion(1+);

Suppliers and Price of 1H-Indole-5-carboxylic acid

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

Atlantic Research Chemicals
1H-Indole-5-carboxylicacid 95%
10gm:
$ 95.43

Total 12 raw suppliers

Chemical Property of 1H-Indole-5-carboxylic acid

Chemical Property:

PSA：53.09000
LogP:1.86610

Purity/Quality:

98%min ^*data from raw suppliers

1H-Indole-5-carboxylicacid 95% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Statements: 21/22-36/37/38
Safety Statements: 26-36/37/39

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 1H-Indole-5-carboxylic acid

There total 17 articles about 1H-Indole-5-carboxylic acid 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: 100.0%

: 1011-65-0
5-methoxycarbonylindole

: 1670-81-1,142396-03-0
1H-Indole-5-carboxylic acid

Guidance literature:: With lithium hydroxide monohydrate; In tetrahydrofuran; water; at 20 ℃; for 90h;
DOI:10.1021/acs.jmedchem.5b00585

Reference yield: 92.0%

: 10075-50-0
5-bromo-1H-indole

: 2258-42-6
formyl acetic anhydride

: 1670-81-1,142396-03-0
1H-Indole-5-carboxylic acid

Guidance literature:: 5-bromo-1H-indole; formyl acetic anhydride; With 1,1'-bis-(diphenylphosphino)ferrocene; palladium diacetate; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 80 - 90 ℃; for 2.5h; Inert atmosphere;

With hydrogenchloride; In water; pH=Ca. 4 - 6;
DOI:10.1080/00397911.2010.528851

Reference yield: 83.0%

: 614-96-0
5-methyl-1H-indole

: 1670-81-1,142396-03-0
1H-Indole-5-carboxylic acid

Guidance literature:: With dipotassium peroxodisulfate; oxygen; CrH₆Mo₆O₂₄^(3-)*3H₃N*3H⁽¹⁺⁾; In water; at 50 ℃; for 24h; under 760.051 Torr; Green chemistry;
DOI:10.1039/d1dt01967h