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1-[(4-ISOTHIOCYANATOPHENYL)SULFONYL]PIPERIDINE is a sulfonyl isothiocyanate derivative of piperidine with the molecular formula C16H19N3O2S. It is a versatile chemical compound used in organic synthesis and chemical research, featuring a piperidine ring and a sulfonyl isothiocyanate group. Its unique chemical structure and properties have been studied for potential therapeutic uses in medicinal chemistry, including as an anti-inflammatory and antimicrobial agent. It serves as an important tool for the development of new drugs and materials in the pharmaceutical and biotechnology industries.

7356-55-0

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7356-55-0 Usage

Uses

Used in Pharmaceutical Industry:
1-[(4-ISOTHIOCYANATOPHENYL)SULFONYL]PIPERIDINE is used as a potential therapeutic agent for its anti-inflammatory and antimicrobial properties, making it a candidate for the development of new drugs to treat various diseases and infections.
Used in Chemical Research:
1-[(4-ISOTHIOCYANATOPHENYL)SULFONYL]PIPERIDINE is used as a versatile compound in organic synthesis for conducting various chemical reactions, contributing to the advancement of chemical knowledge and the creation of new materials.
Used in Biotechnology Industry:
1-[(4-ISOTHIOCYANATOPHENYL)SULFONYL]PIPERIDINE is used as a tool for the development of new materials and technologies in the biotechnology sector, leveraging its unique chemical properties to create innovative solutions for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 7356-55-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,5 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7356-55:
(6*7)+(5*3)+(4*5)+(3*6)+(2*5)+(1*5)=110
110 % 10 = 0
So 7356-55-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H14N2O2S2/c15-18(16,14-8-2-1-3-9-14)12-6-4-11(5-7-12)13-10-17/h4-7H,1-3,8-9H2

7356-55-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-isothiocyanatophenyl)sulfonylpiperidine

1.2 Other means of identification

Product number -
Other names Isothiocyanic acid,(4-piperidinosulfonylphenyl) ester

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:7356-55-0 SDS

7356-55-0Relevant academic research and scientific papers

Synthesis and SAR of selective small molecule neuropeptide y Y2 receptor antagonists

Mittapalli, Gopi Kumar,Vellucci, Danielle,Yang, Jun,Toussaint, Marion,Brothers, Shaun P.,Wahlestedt, Claes,Roberts, Edward

scheme or table, p. 3916 - 3920 (2012/07/03)

Highly potent and selective small molecule neuropeptide Y Y2 receptor antagonists are reported. The systematic SAR exploration of a hit molecule N-(4-ethoxyphenyl)-4-[hydroxy(diphenyl)methyl]piperidine-1-carbothioamide, identified from HTS, led to the discovery of highly potent NPY Y2 antagonists 16 (CYM 9484) and 54 (CYM 9552) with IC50 values of 19 nM and 12 nM respectively.

Synthesis of thiophene-2-carboxamidines containing 2-aminothiazoles and their biological evaluation as urokinase inhibitors

Wilson, Kenneth J.,Illig, Carl R.,Subasinghe, Nalin,Hoffman, James B.,Jonathan Rudolph,Soll, Richard,Molloy, Christopher J.,Bone, Roger,Green, David,Randall, Troy,Zhang, Marie,Lewandowski, Frank A.,Zhou, Zhao,Sharp, Celia,Maguire, Diane,Grasberger, Bruce,DesJarlais, Renee L.,Spurlino, John

, p. 915 - 918 (2007/10/03)

The serine protease urokinase (uPa) has been implicated in the progression of both breast and prostate cancer. Utilizing structure based design, the synthesis of a series of substituted 4-[2-amino-1,3-thiazolyl]-thiophene-2-carboxamidines is described. Further optimization of this series by substitution of the terminal amine yielded urokinase inhibitors with excellent activities.

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