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4059-12-5

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4059-12-5 Usage

Molecular structure

Consists of an imidazole ring with a carbonitrile group at position 5, an amino group at position 4, and a phenylmethyl group attached to the amino group.

Molecular weight

178.21 g/mol

Potential applications

Medicinal chemistry as a building block for the synthesis of pharmaceutical compounds.

Biological activity

May have biological activity and could be used as a starting material for the development of new drugs targeting specific protein receptors or enzymes in the human body.

Unique structure

Makes it a valuable intermediate for the preparation of diverse molecular entities with potential therapeutic properties.

Check Digit Verification of cas no

The CAS Registry Mumber 4059-12-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,5 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4059-12:
(6*4)+(5*0)+(4*5)+(3*9)+(2*1)+(1*2)=75
75 % 10 = 5
So 4059-12-5 is a valid CAS Registry Number.

4059-12-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-amino-1-benzylimidazole-5-carbonitrile

1.2 Other means of identification

Product number -
Other names 4-amino-1-benzyl-5-cyanoimidazole

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:4059-12-5 SDS

4059-12-5Relevant articles and documents

Synthesis of Some New Imidazole Derivatives

Ostrowski, S.

, p. 2237 - 2248 (2007/10/02)

N-Protected (CH2Ph, CH3) 4-nitroimidazoles (1) react with carbanions of tert-butyl chloroacetate, chloroacetonitrile and chloroform, affording Vicarious Nucleophilic Substitution of Hydrogen (VNS) products 2, 3, and 7, respectively.These compounds, after

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