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434326-06-4

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434326-06-4 Usage

Chemical Class

Imidazole

Nitro group

Yes

Phenylmethyl group

Yes

Dichloromethyl groups

Two

Industrial and research applications

Pharmaceuticals, agrochemicals, organic synthesis building block

Utilized in

Synthesis of bioactive compounds, chemical transformations reagent

Safety precautions

Potential skin and eye irritation, hazardous if ingested or inhaled

Check Digit Verification of cas no

The CAS Registry Mumber 434326-06-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,4,3,2 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 434326-06:
(8*4)+(7*3)+(6*4)+(5*3)+(4*2)+(3*6)+(2*0)+(1*6)=124
124 % 10 = 4
So 434326-06-4 is a valid CAS Registry Number.

434326-06-4SDS

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 1-benzyl-4-(dichloromethyl)-5-nitroimidazole

1.2 Other means of identification

Product number -
Other names 1-benzyl-4-dichloromethyl-5-nitroimidazole

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:434326-06-4 SDS

434326-06-4Relevant articles and documents

Vicarious nucleophilic substitution of 1-benzyl-5-nitroimidazole, application to the synthesis of 6,7-dihydroimidazo[4,5-d][1,3]diazepin-8(3H)-one

Chen, Bang-Chi,Chao, Sam T.,Sundeen, Joseph E.,Tellew, John,Ahmad, Saleem

, p. 1595 - 1596 (2007/10/03)

Reaction of 1-benzyl-5-nitroimidazole with carbanion generated from chloroform and potassium tert-butoxide afforded 1-benzyl-4-dichloromethyl-5-nitroimidazole in 72% yield. This vicarious nucleophilic substitution reaction was successfully applied to the synthesis of 6,7-dihydroimidazo[4,5-d][1,3]diazepin-8(3H)-one, an important intermediate in the synthesis of natural and biologically active compounds.

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