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N-Benzyloxycarbonyl-4-piperidinesulfonyl chloride is a chemical compound that plays a significant role in the field of organic chemistry. As a sulfonamide type organic compound, it is involved in various chemical reactions, particularly in the synthesis of other complex organic compounds. N-BENZYLOXYCARBONYL-4-PIPERIDINESULFONYL CHLORIDE is also notable for containing the benzyloxycarbonyl (also known as the carbobenzoxy or Cbz) protective group, which is commonly used in peptide synthesis. Its properties and applications in chemical reactions render it a valuable substance in pharmaceutical and biochemical research. However, due to its potential reactivity and toxicity, it is essential to handle and store N-BENZYLOXYCARBONYL-4-PIPERIDINESULFONYL CHLORIDE with caution.

287953-54-2

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287953-54-2 Usage

Uses

Used in Pharmaceutical and Biochemical Research:
N-Benzyloxycarbonyl-4-piperidinesulfonyl chloride is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its presence in chemical reactions facilitates the creation of complex organic molecules, which are crucial for the development of new drugs and therapeutic agents.
Used in Organic Chemistry:
In the realm of organic chemistry, N-Benzyloxycarbonyl-4-piperidinesulfonyl chloride is used as a reagent in the formation of new chemical bonds and the synthesis of complex organic molecules. Its role in these reactions is essential for advancing the field and discovering new chemical entities.
Used in Peptide Synthesis:
Due to the presence of the benzyloxycarbonyl protective group, N-Benzyloxycarbonyl-4-piperidinesulfonyl chloride is used as a protecting agent in peptide synthesis. This group helps prevent unwanted side reactions during the synthesis process, ensuring the formation of the desired peptide sequence.

Check Digit Verification of cas no

The CAS Registry Mumber 287953-54-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,7,9,5 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 287953-54:
(8*2)+(7*8)+(6*7)+(5*9)+(4*5)+(3*3)+(2*5)+(1*4)=202
202 % 10 = 2
So 287953-54-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H16ClNO4S/c14-20(17,18)12-6-8-15(9-7-12)13(16)19-10-11-4-2-1-3-5-11/h1-5,12H,6-10H2

287953-54-2SDS

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 benzyl 4-chlorosulfonylpiperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names N-Benzoyloxycarbonyl-4-piperidine sulfonyl chloride

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:287953-54-2 SDS

287953-54-2Relevant academic research and scientific papers

NOVEL SULFONAMIDE CARBOXAMIDE COMPOUNDS

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, (2019/01/21)

The present invention relates to compounds of formula (I) wherein Q is selected from O or S; R1 is a non-aromatic heterocyclic group comprising at least one ring nitrogen atom, wherein R1 is attached to the sulfur atom of the sulfonylurea group by a ring carbon atom, and wherein R1 may optionally be substituted; and R2 is a cyclic group substituted at the α-position, wherein R2 may optionally be further substituted. The present invention further relates to salts, solvates and prodrugs of such compounds, to pharmaceutical compositions comprising such compounds, and to the use of such compounds in the treatment and prevention of medical disorders and diseases, most especially by the inhibition of NLRP3.

A library of conformationally restricted saturated heterocyclic sulfonyl chlorides

Zhersh, Sergey,Buryanov, Volodymyr V.,Karpenko, Oleksandr V.,Grygorenko, Oleksandr O.,Tolmachev, Andrey A.

, p. 3669 - 3674 (2011/12/16)

An approach to the synthesis of conformationally restricted saturated heterocyclic sulfonyl chlorides is described. Being guided by the principle of diversity-oriented conformational restriction, a mini-library of saturated heterocyclic sulfonyl chlorides

1-(4-PIPERIDINYL) BENZIMIDAZOLONES AS HISTAMINE H3 ANTAGONISTS

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Page 44-45, (2010/02/04)

Disclosed are histamine H3 antagonists of the formula (I) wherein R1 is benzimidazolone derivative, M1 and M2 are optionally substituted carbon or nitrogen, R2 includes optionally substituted aryl or heteroaryl, and the remaining variables are as defined

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