Methyl 3-methyl-1H-indole-2-carboxylate

Base Information

Chemical Name:Methyl 3-methyl-1H-indole-2-carboxylate
CAS No.:104711-29-7
Molecular Formula:C11H11NO2
Molecular Weight:189.214
Hs Code.:
DSSTox Substance ID:DTXSID10396486
Nikkaji Number:J2.988.758F
Wikidata:Q82197230
Mol file:104711-29-7.mol

Synonyms:Methyl 3-methyl-1H-indole-2-carboxylate;104711-29-7;SCHEMBL5508274;DTXSID10396486;MFCD00159878;Methyl3-methyl-1H-indole-2-carboxylate;CS-0311593;3-Methyl-1H-indole-2-carboxylic acid methyl ester

Suppliers and Price of Methyl 3-methyl-1H-indole-2-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

Total 3 raw suppliers

Chemical Property of Methyl 3-methyl-1H-indole-2-carboxylate

Chemical Property:

XLogP3:2.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:189.078978594
Heavy Atom Count:14
Complexity:229

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(NC2=CC=CC=C12)C(=O)OC

Technology Process of Methyl 3-methyl-1H-indole-2-carboxylate

There total 1 articles about Methyl 3-methyl-1H-indole-2-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: 90.0%

: 67-56-1
methanol

: 83-34-1
3-Methylindole

: 558-13-4
carbon tetrabromide

: 104711-29-7
methyl 3-methyl-1H-indole-2-carboxylate

Guidance literature:: With Ru(2,2'-bipyridine)3(PF₆)2*H₂O; diisopropylamine; at 20 ℃; for 6h; Reagent/catalyst; Concentration; Wavelength; regioselective reaction; Schlenk technique; Inert atmosphere; Irradiation;
DOI:10.1002/chem.201503787

Reference yield: 100.0%

: 104711-29-7
methyl 3-methyl-1H-indole-2-carboxylate

: 10590-73-5
3-methylindole-2-carboxylic acid

Guidance literature:: With sodium hydroxide; In 1,4-dioxane; at 20 ℃;

Reference yield:

: 104711-29-7
methyl 3-methyl-1H-indole-2-carboxylate

: 100-39-0
benzyl bromide

: 1-benzyl-3-methylindole-2-carboxylic acid

Guidance literature:: methyl 3-methyl-1H-indole-2-carboxylate; With sodium hydride; In tetrahydrofuran; N,N-dimethyl-formamide; mineral oil; at 80 ℃; for 0.0833333h; Microwave irradiation;

benzyl bromide; In tetrahydrofuran; N,N-dimethyl-formamide; mineral oil; at 80 ℃; for 0.5h; regioselective reaction; Microwave irradiation;
DOI:10.1039/d0ob02185g