2-[(1H-Benzimidazole-2-sulfinyl)methyl]-N-methylaniline

Base Information

Chemical Name:2-[(1H-Benzimidazole-2-sulfinyl)methyl]-N-methylaniline
CAS No.:104340-37-6
Molecular Formula:C15H15N3OS
Molecular Weight:285.37
Hs Code.:
ChEMBL ID:CHEMBL282226
DSSTox Substance ID:DTXSID10545972
Nikkaji Number:J386.977F
Mol file:104340-37-6.mol

Synonyms:CHEMBL282226;104340-37-6;SCHEMBL6476005;2-[(1H-Benzimidazole-2-sulfinyl)methyl]-N-methylaniline;DTXSID10545972;BDBM50018890;[2-(1H-Benzoimidazole-2-sulfinylmethyl)-phenyl]-methyl-amine

Suppliers and Price of 2-[(1H-Benzimidazole-2-sulfinyl)methyl]-N-methylaniline

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 2-[(1H-Benzimidazole-2-sulfinyl)methyl]-N-methylaniline

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:285.09358328
Heavy Atom Count:20
Complexity:352

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CNC1=CC=CC=C1CS(=O)C2=NC3=CC=CC=C3N2

Technology Process of 2-[(1H-Benzimidazole-2-sulfinyl)methyl]-N-methylaniline

There total 4 articles about 2-[(1H-Benzimidazole-2-sulfinyl)methyl]-N-methylaniline 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: 39.0%

: 104340-35-4
2-[(1H-Benzimidazol-2-yl)thiomethyl]-N-methylbenzenamine

: 104340-37-6
2-[(1H-benzimidazol-2-ylsulfinyl)methyl]-N-methylbenzenamine

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In chloroform; at -10 ℃; for 0.5h;
DOI:10.1021/jm00401a024

Reference yield:

: 100376-52-1
2-methylaminobenzyl chloride

: 104340-37-6
2-[(1H-benzimidazol-2-ylsulfinyl)methyl]-N-methylbenzenamine

Guidance literature:: Multi-step reaction with 2 steps

1: 55 percent / ethanol / 2 h

2: 39 percent / 85percent m-CPBA / CHCl₃ / 0.5 h / -10 °C

With 3-chloro-benzenecarboperoxoic acid; In ethanol; chloroform;
DOI:10.1021/jm00401a024

Reference yield:

: 134469-07-1
Benzimidazol-2-thiol

: 104340-37-6
2-[(1H-benzimidazol-2-ylsulfinyl)methyl]-N-methylbenzenamine

Guidance literature:: Multi-step reaction with 2 steps

1: 55 percent / ethanol / 2 h

2: 39 percent / 85percent m-CPBA / CHCl₃ / 0.5 h / -10 °C

With 3-chloro-benzenecarboperoxoic acid; In ethanol; chloroform;
DOI:10.1021/jm00401a024