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38345-23-2

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38345-23-2 Usage

General Description

3-PHENYL-4H-1,2,4-TRIAZOL-4-AMINE is a chemical compound belonging to the triazole class of organic compounds. It is a derivative of 1,2,4-triazole and is also known as 3-phenyl-1,2,4-triazol-4-amine. 3-PHENYL-4H-1,2,4-TRIAZOL-4-AMINE has a phenyl group attached to the triazole ring and is commonly used in the synthesis of pharmaceuticals and agrochemicals. It has potential biological activity and may exhibit anti-cancer, anti-inflammatory, and anti-microbial properties. Its chemical structure and reactivity make it an important intermediate for the development of various organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 38345-23-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,3,4 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 38345-23:
(7*3)+(6*8)+(5*3)+(4*4)+(3*5)+(2*2)+(1*3)=122
122 % 10 = 2
So 38345-23-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H8N4/c9-12-6-10-11-8(12)7-4-2-1-3-5-7/h1-6H,9H2

38345-23-2SDS

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 3-phenyl-1,2,4-triazol-4-amine

1.2 Other means of identification

Product number -
Other names 4-amino-3-phenyl-1,2,4-triazole

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:38345-23-2 SDS

38345-23-2Relevant articles and documents

Thermal rearrangement of allyl substituted unsymmetric 4H-1,2,4-triazoles to the corresponding 1H-1,2,4-triazoles

Jorgensen, Kare B.,Olsen, Ragnhild B.,Carlsen, Per H.J.

, p. 481 - 495 (2007/10/03)

A series of neat 4-(2-alkenyl) substituted 5-methyl-3-phenyl-4H-1,2,4- triazoles were thermolyzed at 320°C producing a rearrangement products, of which the regioisomeric 1- and 2-substituted triazoles were the main products. The group migrations were rationalized in terms of consecutive S N2-type reactions. This mechanism was supported by a study of the alkylations of the triazoles which gave similar product mixtures. 4-(2-alkenyl) substituted 3-phenyl-4H-1,2,4-triazoles, on the other hand, gave predominantly elimination products.

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