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4886-29-7

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4886-29-7 Usage

General Description

1H-Benzimidazole, 5-chloro-2-(1-methylethyl) (9CI) is a chemical compound with the molecular formula C10H10ClN3. It is a benzimidazole derivative with a chloro substituent at the 5-position and an isopropyl group at the 2-position. This chemical is used in the synthesis of pharmaceuticals, particularly as a building block in the production of various drugs. It has also been studied for its potential biological activities, including its potential as an antifungal and antibacterial agent. Additionally, it has been investigated for its potential as a ligand in coordination chemistry and for its environmental impact.

Check Digit Verification of cas no

The CAS Registry Mumber 4886-29-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,8 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4886-29:
(6*4)+(5*8)+(4*8)+(3*6)+(2*2)+(1*9)=127
127 % 10 = 7
So 4886-29-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H11ClN2/c1-6(2)10-12-8-4-3-7(11)5-9(8)13-10/h3-6H,1-2H3,(H,12,13)

4886-29-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-2-propan-2-yl-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names Benzimidazole,5-chloro-2-isopropyl

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:4886-29-7 SDS

4886-29-7Downstream Products

4886-29-7Relevant articles and documents

Synthesis of 2-alkyl-substituted benzimidazoles by thermal decomposition of 2-azidobenzenamines in the presence of an aldehyde

Wallace, Jeffery M.,Soederberg, Bjoern C. G.,Hubbard, Jeremiah W.

, p. 3425 - 3439 (2007/10/03)

2-Substituted benzimidazoles were prepared by reaction of 2-azidoaminobenzenes with aldehydes under thermal conditions. The reaction probably proceeds via a sequential imine formation, azide decomposition forming a nitrene, and electrocyclization. Copyright Taylor & Francis Group, LLC.

SYNTHESIS AND PESTICIDAL ACTIVITY OF N,N'-DIACYL DERIVATIVES OF 4-CHLORO-1,2-PHENYLENDIAMINE

Molchanov, L. V.,Ayupova, A. T.,Kadyrov, Ch. Sh.,Shapkin, V. A.

, p. 196 - 198 (2007/10/02)

The acylation of 2-aminoacyl-chloroanilines with acid anhydrides has given N,N'-diacyl derivatives of 4-chloro-1,2-phenylenediamine.Their fungicidal activities have been investigated.It has been shown that in cotton plants they are converted into 2-alkyl-5-chlorobenzimidazoles.

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