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N-[(4-methylphenyl)sulfonyl]hexanamide is a chemical compound with the molecular formula C13H21NO3S. It is a derivative of hexanamide, featuring a sulfonyl group attached to a 4-methylphenyl ring. N-[(4-methylphenyl)sulfonyl]hexanamide is characterized by its amide and sulfonyl functional groups, which contribute to its chemical reactivity and potential applications in various fields, such as pharmaceuticals and chemical synthesis. The presence of the 4-methylphenyl group provides a unique structural feature that can influence its physical and chemical properties, making it a potentially valuable building block in the development of new compounds with specific therapeutic or industrial uses.

1788-15-4

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1788-15-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1788-15-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,8 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1788-15:
(6*1)+(5*7)+(4*8)+(3*8)+(2*1)+(1*5)=104
104 % 10 = 4
So 1788-15-4 is a valid CAS Registry Number.

1788-15-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-methylphenyl)sulfonylhexanamide

1.2 Other means of identification

Product number -
Other names N-hexanoyl-4-methylbenzenesulfonamide

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:1788-15-4 SDS

1788-15-4Downstream Products

1788-15-4Relevant academic research and scientific papers

A novel and efficient solvent-free and heterogeneous method for the synthesis of primary, secondary and bis-N-acylsulfonamides using metal hydrogen sulfate catalysts

Massah, Ahmad Reza,Asadi, Beheshteh,Hoseinpour, Mahdieh,Molseghi, Azadeh,Kalbasi, Roozbeh Javad,Javaherian Naghash, Hamid

experimental part, p. 7696 - 7705 (2009/12/04)

Some metal hydrogen sulfates were used as acid catalysts in the N-acylation of different sulfonamides using carboxylic acid chlorides and anhydrides as acylating agents under both heterogeneous and solvent-free conditions. Al(HSO4)3

Sulfamidation of 2-arylaldehydes and ketones with chloramine-T

Baumann, Thomas,Bachle, Michael,Brase, Stefan

, p. 3797 - 3800 (2007/10/03)

A series of aliphatic and aromatic carbonyl compounds has been transformed into the corresponding sulfamidated products by means of amine-catalyzed nitrene transfer of chloramine-T. Depending on the residues R, either α-sulfamidation in the case of aromat

Copper-catalyzed hydrative amide synthesis with terminal alkyne, sulfonyl azide, and water

Cho, Seung Hwan,Yoo, Eun Jeong,Bae, Imhyuck,Chang, Sukbok

, p. 16046 - 16047 (2007/10/03)

It is shown for the first time that N-sulfonyl amides can be efficiently prepared by an unconventional approach of the hydrative reaction between terminal alkynes, sulfonyl azides, and water in the presence of copper catalyst and amine base under very mil

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