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75918-79-5

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75918-79-5 Usage

Family

Triazole family

Heterocycle

Five-membered ring containing three nitrogen atoms and two carbon atoms

Phenyl groups

Attached to the 1 and 4 positions of the triazole ring

Carbaldehyde group

Attached to the 5 position of the triazole ring

Organic chemistry

Used in the synthesis of various compounds

Pharmaceuticals

Potential use in the development of new drugs

Agrochemicals

Potential use in the development of new pesticides or fertilizers

Materials science

Potential use in the development of new materials

Coordination chemistry

Potential use in the formation of coordination complexes

Building block

Can be used as a starting point for the synthesis of more complex organic molecules

Check Digit Verification of cas no

The CAS Registry Mumber 75918-79-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,9,1 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75918-79:
(7*7)+(6*5)+(5*9)+(4*1)+(3*8)+(2*7)+(1*9)=175
175 % 10 = 5
So 75918-79-5 is a valid CAS Registry Number.

75918-79-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-diphenyltriazole-4-carbaldehyde

1.2 Other means of identification

Product number -
Other names 1,4-diphenyl-1h-1,2,3-triazole-5-carbaldehyde

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:75918-79-5 SDS

75918-79-5Relevant articles and documents

Cycloaddition of organic azides to α,β-acetylenic aldimines

Piterskaya,Khramchikhin,Stadnichuk,Bel'skii,Stash

, p. 1150 - 1157 (2007/10/03)

The reaction selectivity of aryl azides with α,β-acetylenic aldimines R1C≡C-CH=NR2 is independent of R1 and R2: the addition always occurs chemospecifically at the triple bond and results in formation of 1-aryl-

Reaction of a Triazolylcarbene with the Xylenes and Mesitylene and the Resulting Norcaradiene-Tropilidene Rearrangements

Bedford, C. D.,Bruckmann, E. M.,Smith, P. A. S.

, p. 679 - 686 (2007/10/02)

An improved synthesis of 5-(diazomethyl)-1,4-diphenyl-1,2,3-triazole (1) has been developed.It fragments to a carbene at 40-50 deg C and reacts with o-, m-, or p-xylene or indan at 40-50 deg C to give high yields of cycloheptatriene products, presumably t

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