Carbamodithioic acid, (1H-indol-2-ylmethyl)-, methyl ester

Base Information

Chemical Name:Carbamodithioic acid, (1H-indol-2-ylmethyl)-, methyl ester
CAS No.:881853-68-5
Molecular Formula:C11H12N2S2
Molecular Weight:236.362
Hs Code.:
ChEMBL ID:CHEMBL220267
DSSTox Substance ID:DTXSID10470275
Wikidata:Q82298314

Synonyms:881853-68-5;Methyl ((1H-indol-2-yl)methyl)carbamodithioate;Carbamodithioic acid, (1H-indol-2-ylmethyl)-, methyl ester;CHEMBL220267;SCHEMBL12993634;DTXSID10470275;AKOS015965296;methyl (indol-2-yl)methyldithiocarbamate;2-(S-methyldithiocarbamoylaminomethyl)indole

Suppliers and Price of Carbamodithioic acid, (1H-indol-2-ylmethyl)-, methyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Carbamodithioic acid, (1H-indol-2-ylmethyl)-, methyl ester

Chemical Property:

XLogP3:2.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:236.04419074
Heavy Atom Count:15
Complexity:233

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CSC(=S)NCC1=CC2=CC=CC=C2N1

Technology Process of Carbamodithioic acid, (1H-indol-2-ylmethyl)-, methyl ester

There total 1 articles about Carbamodithioic acid, (1H-indol-2-ylmethyl)-, methyl 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: 85.0%

: 75-15-0,12122-00-8
carbon disulfide

: 21109-25-1
1-(1H-indol-2-yl)methanamine

: 74-88-4
methyl iodide

: 881853-68-5
isobrassinin

Guidance literature:: carbon disulfide; 1-(1H-indol-2-yl)methanamine; With dmap; triethylamine; In chloroform; at 0 - 20 ℃; for 2h;

methyl iodide; In chloroform; at 20 ℃; for 3h;
DOI:10.1016/j.bmcl.2006.09.016