1H-Benzimidazole, 2-[(phenylmethyl)sulfinyl]-

Base Information

Chemical Name:1H-Benzimidazole, 2-[(phenylmethyl)sulfinyl]-
CAS No.:104340-32-1
Molecular Formula:C14H12N2OS
Molecular Weight:256.328
Hs Code.:
DSSTox Substance ID:DTXSID50545971
Nikkaji Number:J2.597.989C
Mol file:104340-32-1.mol

Synonyms:104340-32-1;1H-Benzimidazole, 2-[(phenylmethyl)sulfinyl]-;2-benzylsulfinyl-1h-benzimidazole;2-(Phenylmethanesulfinyl)-1H-benzimidazole;SCHEMBL636639;DTXSID50545971

Suppliers and Price of 1H-Benzimidazole, 2-[(phenylmethyl)sulfinyl]-

Supply Marketing:

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

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Chemical Property of 1H-Benzimidazole, 2-[(phenylmethyl)sulfinyl]-

Chemical Property:

XLogP3:2.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:256.06703418
Heavy Atom Count:18
Complexity:304

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

Technology Process of 1H-Benzimidazole, 2-[(phenylmethyl)sulfinyl]-

There total 12 articles about 1H-Benzimidazole, 2-[(phenylmethyl)sulfinyl]- 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: 96.0%

: 51290-77-8
2-(benzylthio)-1H-benzo[d]imidazole

: 104340-32-1
(benzimidazol-2-yl) benzyl sulfoxide

Guidance literature:: With chloro-trimethyl-silane; dihydrogen peroxide; In water; acetonitrile; at 25 ℃; for 0.166667h; chemoselective reaction;
DOI:10.1016/j.tetlet.2010.10.171

Reference yield:

: 134469-07-1
Benzimidazol-2-thiol

: 104340-32-1
(benzimidazol-2-yl) benzyl sulfoxide

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydroxide / ethanol; H₂O / 2.5 h / Heating

2: m-chloroperbenzoic acid / CHCl₃ / 0.17 h / 0 - 5 °C

With sodium hydroxide; 3-chloro-benzenecarboperoxoic acid; In ethanol; chloroform; water;
DOI:10.1021/jo00229a039

Reference yield:

: 7152-24-1
2-methylsulfanylbenzimidazole

: 104340-32-1
(benzimidazol-2-yl) benzyl sulfoxide

Guidance literature:: Multi-step reaction with 3 steps

1: m-chloroperbenzoic acid / CHCl₃ / 0.17 h / 0 - 5 °C

2: aq. ethanol / 25 °C

3: m-chloroperbenzoic acid / CHCl₃ / 0.17 h / 0 - 5 °C

With 3-chloro-benzenecarboperoxoic acid; In ethanol; chloroform;
DOI:10.1021/jo00229a039