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3H-1,2,4-Triazole-3-thione, 2,4-dihydro-2-methyl-4-phenyl- is a chemical compound with the molecular formula C9H9N3S. It is a derivative of 1,2,4-triazole, a five-membered heterocyclic ring containing three nitrogen atoms and one sulfur atom. This specific compound features a methyl group at the 2-position and a phenyl group at the 4-position, which are both attached to the triazole ring. The compound is classified as a 3H-1,2,4-triazole-3-thione, indicating the presence of a thione group (a sulfur analog of a ketone) at the 3-position. This chemical is primarily used in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity.

2360-40-9

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2360-40-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2360-40-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,6 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2360-40:
(6*2)+(5*3)+(4*6)+(3*0)+(2*4)+(1*0)=59
59 % 10 = 9
So 2360-40-9 is a valid CAS Registry Number.

2360-40-9SDS

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 2-methyl-4-phenyl-2,4-dihydro-[1,2,4]triazole-3-thione

1.2 Other means of identification

Product number -
Other names 2-Methyl-4-phenyl-2,4-dihydro-[1,2,4]triazol-3-thion

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:2360-40-9 SDS

2360-40-9Relevant academic research and scientific papers

A Study of the Behaviour of 2,4-Substituted Thiosemicarbazides toward Orthoesters: Formation of Mesoionic Compounds

Buccheri, Francesco,Cusmano, Giuseppe,Gruttadauria, Michelangelo,Noto, Renato,Werber, Giuseppe

, p. 1447 - 1451 (2007/10/03)

The reactions beetwen 2,4-disubstituted thiosemicarbazides and orthoesters in refluxing xylene led to the formation of the 1,2,4-triazoline-5-thione ring and to the 1,2,4-triazolium-5-thiolate ring. The formation of the mesoionic componds is due to rearrangement of the easily available 2,4-disubstituted thiosemicarbazides to 1,4-disubstituted thiosemicarbazides under the reaction conditions adopted. This method can be usefully used for the synthesis of mesoionic compounds, especially in the case of the 2-methyl-4-phenylthiosemicarbazide.

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