2-[(1H-Benzimidazole-2-sulfinyl)methyl]aniline

Base Information

Chemical Name:2-[(1H-Benzimidazole-2-sulfinyl)methyl]aniline
CAS No.:104340-34-3
Molecular Formula:C14H13N3OS
Molecular Weight:271.343
Hs Code.:
ChEMBL ID:CHEMBL20032
DSSTox Substance ID:DTXSID70543212
Nikkaji Number:J386.973C
Mol file:104340-34-3.mol

Synonyms:CHEMBL20032;104340-34-3;2-[(1H-Benzimidazole-2-sulfinyl)methyl]aniline;SCHEMBL6475609;DTXSID70543212;INGIXPMMNAFVHF-UHFFFAOYSA-N;BDBM50018873;2-(1H-Benzoimidazole-2-sulfinylmethyl)-phenylamine;2-[(1H-Benzimidazol-2-yl)sulfinylmethyl]benzenamine;2-[(1H-Benzimidazol-2-ylsulfinyl)methyl]benzenamine

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

Supply Marketing:

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

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

Chemical Property:

XLogP3:1.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:271.07793322
Heavy Atom Count:19
Complexity:339

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C(=C1)CS(=O)C2=NC3=CC=CC=C3N2)N

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

There total 9 articles about 2-[(1H-Benzimidazole-2-sulfinyl)methyl]aniline 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: 97.4%

: 104340-33-2
2-<(1H-benzimidazol-2-ylthio)methyl>aniline

: 104340-34-3
2-[(1H-benzimidazol-2-ylsulfinyl)methyl]benzenamine

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In methanol; chloroform; at -5 ℃; for 0.5h;
DOI:10.1016/0223-5234(91)90024-H

Reference yield:

: 75-18-3
dimethylsulfide

: 104340-33-2
2-<(1H-benzimidazol-2-ylthio)methyl>aniline

: 104340-34-3
2-[(1H-benzimidazol-2-ylsulfinyl)methyl]benzenamine

Guidance literature:: With m-chloroperoxybenzoic acid; In chloroform;

Reference yield:

: 5344-90-1
2-Aminobenzyl alcohol

: 104340-34-3
2-[(1H-benzimidazol-2-ylsulfinyl)methyl]benzenamine

Guidance literature:: Multi-step reaction with 2 steps

1: 20 percent / H₂SO₄ / acetic acid / 3 h / 84 °C

2: 60 percent / 85percent m-CPBA / CHCl₃ / 0.5 h / -10 °C

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