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1H-Benzimidazole, 2-[2-(methylthio)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62871-44-7

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62871-44-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62871-44-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,8,7 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 62871-44:
(7*6)+(6*2)+(5*8)+(4*7)+(3*1)+(2*4)+(1*4)=137
137 % 10 = 7
So 62871-44-7 is a valid CAS Registry Number.

62871-44-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-methylsulfanylphenyl)-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names 1H-Benzimidazole,2-[2-(methylthio)phenyl]

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:62871-44-7 SDS

62871-44-7Downstream Products

62871-44-7Relevant academic research and scientific papers

Synthesis, characterization and coordination properties of 2-(2′-(methylseleno)phenyl)benzimidazole

Dutta, Pradip Kr.,Panda, Snigdha,Zade, Sanjio S.

, p. 83 - 89 (2014/01/17)

2-(2′-(methylseleno)phenyl)benzimidazole (1) was synthesized from 2-(methylseleno)benzaldehyde and 1,2-diaminobenzene in presence of acetic acid as a catalyst. The reaction of 1 with Pd(II) and Pt(II) afforded square planar complexes 4 and 5 with metal li

N-hydroxyphthalimide/cobalt acetate, a new catalytic oxidative system for the synthesis of benzimidazoles

Coppola, Gary M.

, p. 3500 - 3507 (2008/12/23)

Benzimidazoles are readily prepared from 1,2-phenylenediamine and an aldehyde using air and catalytic N-hydroxyphthalimide/Co(OAc)2 as the oxidant. Both electron-donating and electron-withdrawing groups are tolerated. Copyright Taylor & Francis Group, LLC.

2-Pyridinyl-phenyl-sulphinyl-and-phenyl-thio-benzimidazoles having antiflammatory or gastic acid secretion inhibition activity

-

, (2008/06/13)

Compounds of formula I, STR1 in which A is a 5 or 6 membered, fully unsaturated, carbocyclic or heterocyclic ring, B is a 5 or 6 membered, fully unsaturated, nitrogen containing heterocyclic ring, X is NR19, O or S, R19 is hydrogen or alkyl optionally substituted by --OCOR, n is 0 or 1, R3, R4, R5, R6, R7, R8, R9 and R10 have various significances, R1 and R2, are hydrogen or alkyl or together with the ring carbon atoms to which they are attached, form a benzene or pyridine ring, which ring carries substituents R15, R16, R17 and R18, R15, R16, R17 and R18, have various significances, with certain provisos are described. Processes for making the compounds and pharmaceutical formulations containing them, e.g. for the treatment of conditions including excess gastric acid secretion, are also described.

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