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4-Piperidinecarbothioamide, also known as thiazepine, is a heterocyclic organic compound with a molecular formula of C6H12N2S. It is a sulfur-containing compound derived from piperidine and has been found to exhibit various biological activities, including antimicrobial, anticonvulsant, and analgesic properties. Its unique structure and properties make it a promising candidate for use in pharmaceuticals and agrochemicals, as well as in industrial applications as a corrosion inhibitor.

112401-09-9

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112401-09-9 Usage

Uses

Used in Pharmaceutical Industry:
4-Piperidinecarbothioamide is used as a building block for the synthesis of pharmaceuticals due to its various biological activities. Its antimicrobial, anticonvulsant, and analgesic properties make it a valuable component in the development of new drugs to treat a range of medical conditions.
Used in Agrochemical Industry:
4-Piperidinecarbothioamide is used as a building block in the synthesis of agrochemicals, where its antimicrobial properties can be utilized to develop new pesticides and other agricultural products to protect crops and enhance agricultural productivity.
Used in Industrial Applications:
4-Piperidinecarbothioamide is used as a corrosion inhibitor in industrial applications. Its ability to prevent the corrosion of metals can be applied in various industries, such as oil and gas, automotive, and construction, to extend the lifespan of metal equipment and structures, thereby reducing maintenance costs and improving safety.

Check Digit Verification of cas no

The CAS Registry Mumber 112401-09-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,4,0 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 112401-09:
(8*1)+(7*1)+(6*2)+(5*4)+(4*0)+(3*1)+(2*0)+(1*9)=59
59 % 10 = 9
So 112401-09-9 is a valid CAS Registry Number.

112401-09-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Piperidinecarbothioamide

1.2 Other means of identification

Product number -
Other names 4-thiocarbamoyl-piperidine

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:112401-09-9 SDS

112401-09-9Relevant academic research and scientific papers

PROCESSES FOR CONVERTING CARBOXAMIDES TO THIOCARBOXAMIDES

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Paragraph 0076; 0077; 0078; 0079; 0080; 0081; 0082, (2016/11/28)

Process for converting a carboxamide to a thiocarboxamide includes reacting (a) a substrate that comprises a heteroatom-containing moiety and a carboxamide moiety with (b) a dialkyl dithiophosphate and/or a salt thereof. The heteroatom-containing moiety includes a heteroatom selected from the group consisting of N, O, and S. Processes for preparing piperidine-4-thiocarboxamide are described.

PREPARATION OF PIPERIDINE-4-CARBOTHIOAMIDE

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Page/Page column 4, (2016/01/01)

The present invention describes a novel process for preparing piperidine-4-carbothioamide.

INDOLE DERIVATIVE WITH 5HT1A AFFINITY

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Page/Page column 32-33, (2008/06/13)

Novel indole derivatives of formula (I), where A , X, R1, R1' and m have the meanings given in claim 1, have a strong affinity for the 5-HT1A and partial affinity for the 5-HT1D receptors. The compounds inhibit serotonin reuptake, display serotonin agonist and antagonist properties and are suitable as antidepressants, anxiolytics and for the treatment of neurodegenerative diseases.

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