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3-Chloro-propane-1-sulfonic acid tert-butylamide, a chemical compound with the formula C7H16ClNO3S, is a derivative of propane sulfonic acid. It is a white to off-white solid with a high melting point and is soluble in both water and organic solvents. This versatile compound is often used as a reagent in organic synthesis and serves as an intermediate in the production of pharmaceuticals and agrochemicals.

63132-85-4

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63132-85-4 Usage

Uses

Used in Organic Synthesis:
3-Chloro-propane-1-sulfonic acid tert-butylamide is used as a reagent in organic synthesis for its ability to participate in various chemical reactions, contributing to the formation of a wide range of compounds.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 3-chloro-propane-1-sulfonic acid tert-butylamide is utilized as an intermediate in the manufacturing process of various drugs, playing a crucial role in the synthesis of active pharmaceutical ingredients.
Used in Agrochemical Production:
Similarly, in the agrochemical sector, 3-CHLORO-PROPANE-1-SULFONIC ACID TERT-BUTYLAMIDE is employed as an intermediate for the production of various agrochemicals, aiding in the development of substances used in agriculture to protect crops and enhance yields.
Used in Dye and Pigment Manufacturing:
3-Chloro-propane-1-sulfonic acid tert-butylamide is also used in the manufacturing of dyes and pigments, where its chemical properties contribute to the creation of a diverse palette of colors for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 63132-85-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,1,3 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 63132-85:
(7*6)+(6*3)+(5*1)+(4*3)+(3*2)+(2*8)+(1*5)=104
104 % 10 = 4
So 63132-85-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H16ClNO2S/c1-7(2,3)9-12(10,11)6-4-5-8/h9H,4-6H2,1-3H3

63132-85-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-tert-butyl-3-chloropropane-1-sulfonamide

1.2 Other means of identification

Product number -
Other names 3-chloro-N-(1,1-dimethylethyl)-1-propanesulfonamide

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:63132-85-4 SDS

63132-85-4Relevant articles and documents

Toward the Synthesis of Fluorinated Analogues of HCV NS3/4A Serine Protease Inhibitors Using Methyl α-Amino-β-fluoro-β-vinylcyclopropanecarboxylate as Key Intermediate

Milanole, Ga?lle,Andriessen, Floris,Lemonnier, Gérald,Sebban, Muriel,Coadou, Ga?l,Couve-Bonnaire, Samuel,Bonfanti, Jean-Fran?ois,Jubault, Philippe,Pannecoucke, Xavier

supporting information, p. 2968 - 2971 (2015/06/30)

Synthesis of fluorocyclopropyl building blocks, which constitute the core of various therapeutic agents against the hepatitis C virus, is described. The relevant methyl α-amino-β-fluoro-β-vinylcyclopropanecarboxylate has been used as a key intermediate for the total synthesis of a fluorinated analogue of Simeprevir (TMC 435), a HCV NS3/4A protease inhibitor.

Preparation of cyclopropyl sulfonylamides

-

Page/Page column 2-3, (2009/05/28)

A novel process for the preparation of cyclopropyl sulfonamide of the formula I is described. Cyclopropyl sulfonamide is a versatile building block for many biologically active compounds.

Hepatitis C Virus Inhibitors

-

Page/Page column 26, (2008/06/13)

Hepatitis C virus inhibitors having the general formula are disclosed. Compositions comprising the compounds and methods for using the compounds to inhibit HCV are also disclosed.

Inhibitors of Hepatitis C Virus

-

Page/Page column 24-25, (2008/12/04)

Macrocyclic peptides are disclosed having the general formula: wherein R3, R3′, R4, R6, R′, X, Q and W are described. Compositions comprising the compounds and methods for using the compounds to inhibit HCV are also disclosed.

MACROCYCLIC PEPTIDES AS HEPATITIS C VIRUS INHIBITORS

-

Page/Page column 50-51, (2008/12/05)

Macrocyclic peptides having the general formula (I): are disclosed. Compositions comprising the compounds and methods for using the compounds to inhibit HCV are also disclosed.

Inhibitors of Hepatitis C Virus

-

Page/Page column 24, (2008/12/04)

Macrocyclic peptides are disclosed having the general formula: wherein R3, R3′, R4, R6, R′, X, Q and W are described. Compositions comprising the compounds and methods for using the compounds to inhibit HCV are also disclosed.

Inhibitors of Hepatitis C Virus

-

Page/Page column 24-25, (2008/12/04)

Macrocyclic peptides are disclosed having the general formula: wherein R3, R′3, R4, R6, R′, X, Q and W are described. Compositions comprising the compounds and methods for using the compounds to inhibit HCV are also disclosed.

Hepatitis C Virus Inhibitors

-

Page/Page column 23-24, (2008/12/05)

Hepatitis C virus inhibitors having the general formula are disclosed. Compositions comprising the compounds and methods for using the compounds to inhibit HCV are also disclosed.

MACROCYCLIC PEPTIDES AS HEPATITIS C VIRUS INHIBITORS

-

Page/Page column 49; 50, (2008/12/05)

Macrocyclic peptides having the general formula are disclosed. Compositions comprising the compounds and methods for using the compounds to inhibit HCV are also disclosed.

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