5-methyl-7-nitro-1H-indole-2-carboxylic acid

Base Information

Chemical Name:5-methyl-7-nitro-1H-indole-2-carboxylic acid
CAS No.:90771-56-5
Molecular Formula:C10H8N2O4
Molecular Weight:220.185
Hs Code.:
DSSTox Substance ID:DTXSID301256338
Mol file:90771-56-5.mol

Synonyms:5-methyl-7-nitro-1H-indole-2-carboxylic acid;90771-56-5;5-Methyl-7-nitroindole-2-carboxylic acid;SCHEMBL2768879;DTXSID301256338;DB-242476;CS-0282027;5-methyl-7-nitro-1H-indole-2-carboxylicacid;EN300-99186

Suppliers and Price of 5-methyl-7-nitro-1H-indole-2-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

Crysdot
5-Methyl-7-nitro-1H-indole-2-carboxylicacid 97%
1g
$ 528.00

Chemenu
5-Methyl-7-nitro-1H-indole-2-carboxylicacid 95%+
1g
$ 498.00

Alichem
5-Methyl-7-nitro-1H-indole-2-carboxylicacid
1g
$ 567.62

Total 6 raw suppliers

Chemical Property of 5-methyl-7-nitro-1H-indole-2-carboxylic acid

Chemical Property:

PSA：98.91000
LogP:2.60590
XLogP3:2.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:220.04840674
Heavy Atom Count:16
Complexity:314

Purity/Quality:

98% ^*data from raw suppliers

5-Methyl-7-nitro-1H-indole-2-carboxylicacid 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC2=C(C(=C1)[N+](=O)[O-])NC(=C2)C(=O)O

Technology Process of 5-methyl-7-nitro-1H-indole-2-carboxylic acid

There total 3 articles about 5-methyl-7-nitro-1H-indole-2-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: 94.0%

: 1120345-02-9
5-methyl-7-nitro-1H-indol-2-carboxylic acid methyl ester

: 90771-56-5
5-methyl-7-nitro-1H-indol-2-carboxylic acid

Guidance literature:: 5-methyl-7-nitro-1H-indol-2-carboxylic acid methyl ester; With lithium hydroxide monohydrate; water; In tetrahydrofuran; methanol; at 20 ℃; for 8h;

With hydrogenchloride; In tetrahydrofuran; methanol; water;