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4-methyl-N-phenylpiperazine-1-carbothioamide is a chemical compound with the molecular formula C12H17N3S. It is a derivative of piperazine, featuring a methyl group at the 4-position and a phenyl group attached to the nitrogen atom. The carbothioamide group is present at the 1-position, which is a thioamide functional group. 4-methyl-N-phenylpiperazine-1-carbothioamide is known for its potential applications in the pharmaceutical industry, particularly as a building block for the synthesis of various drugs. It is also used in the synthesis of certain psychoactive substances. Due to its chemical structure, it can interact with various receptors in the body, which is why it is studied for its potential therapeutic effects and side effects. The compound's properties and reactivity are influenced by the presence of the thioamide group, which can participate in various chemical reactions, making it a versatile intermediate in organic synthesis.

6336-69-2

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6336-69-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6336-69-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6336-69:
(6*6)+(5*3)+(4*3)+(3*6)+(2*6)+(1*9)=102
102 % 10 = 2
So 6336-69-2 is a valid CAS Registry Number.

6336-69-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-piperazine-1-carbodithioic acid methyl ester

1.2 Other means of identification

Product number -
Other names 4-Methyl-piperazin-1-dithiocarbonsaeure-methylester

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:6336-69-2 SDS

6336-69-2Relevant academic research and scientific papers

Synthesis of N-substituted-N-acylthioureas of 4-substituted piperazines endowed with local anaesthetic, antihyperlipidemic, antiproliferative activities and antiarrythmic, analgesic, antiaggregating actions

Ranise, Angelo,Spallarossa, Andrea,Bruno, Olga,Schenone, Silvia,Fossa, Paola,Menozzi, Giulia,Bondavalli, Francesco,Mosti, Luisa,Capuano, Annalisa,Mazzeo, Filomena,Falcone, Giuseppe,Filippelli, Walter

, p. 765 - 780 (2007/10/03)

Three series of N-acyl and N-cyclohexyl- or N-methyl or N-phenyl-thioureas of 4-substituted (methyl, phenyl, 2-pyridyl)piperazines (4-12) were synthesised according to a highly convergent one-pot procedure and tested in vivo (local anaesthetic, anti-hyper

A New Convenient Method of Desulphurisation of Thioureas and Thioamides

Abuzar, Syed,Sharma, Satyavan,Iyer, R. N.

, p. 211 - 212 (2007/10/02)

The action of thiophosgene on thioureas and thioamides provides a convenient method of desulphurisation of these compounds to ureas and amides respectively.

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