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1-(4-azidophenyl)-1H-imidazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71510-50-4

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71510-50-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71510-50-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,5,1 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 71510-50:
(7*7)+(6*1)+(5*5)+(4*1)+(3*0)+(2*5)+(1*0)=94
94 % 10 = 4
So 71510-50-4 is a valid CAS Registry Number.

71510-50-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-azidophenyl)imidazole

1.2 Other means of identification

Product number -
Other names 1H-Imidazole,1-(4-azidophenyl)

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:71510-50-4 SDS

71510-50-4Downstream Products

71510-50-4Relevant academic research and scientific papers

Synthesis of novel heteroarenes based [1,2,3]-triazoles via click chemistry and their evaluation for antibacterial activity

Prasad, Davinder,Aggarwal, Nisha,Kumar, Rajesh,Nath, Mahendra

experimental part, p. 731 - 738 (2012/07/02)

A series of heteroarenes based [1,2,3]-triazole derivatives 8a-h and 9a-f has been synthesized via click chemistry through Huisgen [2+3] cycloaddition reaction of heteroarylazides 7a-e with alkynes (3a-c, propargyl alcohol or phenyl acetylene) in the presence of CuSO4.5H2O and sodium ascorbate in t-butanol and water (1:1) mixture at 25°C in good to excellent yields (74-94%). All the newly synthesized compounds have been characterized on the basis of analytical and spectral data. The compounds 8a, 8e, 9a, 9b, 9c and 9e have been evaluated for their preliminary in-vitro antibacterial efficacy against a panel of two Gram-positive bacteria viz. Staphylococcus aureus and Streptococcus mutans and two Gramnegative bacteria viz. Escherichia coli and Pseudomonas aeruginosa using the Agar disc diffusion method.

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