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4H-1,2,4-Triazol-3-amine, N,4,5-triphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15129-16-5

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15129-16-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15129-16-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,1,2 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15129-16:
(7*1)+(6*5)+(5*1)+(4*2)+(3*9)+(2*1)+(1*6)=85
85 % 10 = 5
So 15129-16-5 is a valid CAS Registry Number.

15129-16-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (4,5-diphenyl-4H-[1,2,4]triazol-3-yl)-phenyl-amine

1.2 Other means of identification

Product number -
Other names (4,5-Diphenyl-4H-[1,2,4]triazol-3-yl)-phenyl-amin

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:15129-16-5 SDS

15129-16-5Relevant academic research and scientific papers

I2-Mediated Oxidative C-N and N-S Bond Formation in Water: A Metal-Free Synthesis of 4,5-Disubstituted/N-Fused 3-Amino-1,2,4-triazoles and 3-Substituted 5-Amino-1,2,4-thiadiazoles

Jatangi, Nagesh,Tumula, Nagaraju,Palakodety, Radha Krishna,Nakka, Mangarao

, p. 5715 - 5723 (2018/05/15)

An environmentally benign and convenient strategy for the synthesis of 4,5-disubstituted/N-fused 3-amino-1,2,4-triazoles and 3-substituted 5-amino-1,2,4-thiadiazoles from isothiocyanates has been developed. This metal-free method involves I2-me

A facile one-pot synthetic method for 1,2,4-triazoles and 1,3-disubstituted thioureas

Singh, Okram Mukherjee,Singh, Sarangthem Joychandra

, p. 483 - 485 (2007/10/03)

The reaction of arylisothiocyanates with triethylamine and acylhydrazides in the presence of mercuric acetate has been studied. The reaction proceeds through the formation of thiourea, followed by a sequential addition-dehydration with acylhydrazides. The initial detection of thiourea, which mediates the formation of disubstituted 1,2,4-triazoles, is explained by a plausible mechanism.

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