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N-(3-chloro-2-oxopropyl)-4-methylbenzenesulfonamide is a chemical compound with the molecular formula C10H10ClNO3S. It is an organic compound that features a benzene ring with a sulfonamide group attached to it, which is a common functional group in various pharmaceuticals and agrochemicals. The compound has a 4-methyl substituent on the benzene ring, indicating a methyl group attached at the 4th position. Additionally, it contains a 3-chloro-2-oxopropyl group, which is a three-carbon chain with a chloro group at the 3rd carbon and a carbonyl group at the 2nd carbon. This chemical structure may contribute to its potential reactivity and applications in chemical synthesis or as an intermediate in the production of other compounds.

4294-36-4

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4294-36-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4294-36-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,9 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4294-36:
(6*4)+(5*2)+(4*9)+(3*4)+(2*3)+(1*6)=94
94 % 10 = 4
So 4294-36-4 is a valid CAS Registry Number.

4294-36-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(3-chloro-2-oxopropyl)-4-methyl-Benzenesulfonamide

1.2 Other means of identification

Product number -
Other names -

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

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More Details:4294-36-4 SDS

4294-36-4Relevant academic research and scientific papers

Chemoselective synthesis of N-substituted α-amino-α′- chloro ketones via chloromethylation of glycine-derived Weinreb amides

Pace, Vittorio,Holzer, Wolfgang,Verniest, Guido,Alcantara, Andres R.,De Kimpe, Norbert

supporting information, p. 919 - 926 (2013/05/08)

Functionalized α-arylamino-α′-chloro ketones are obtained in high yield via a straightforward homologation reaction of Weinreb amides derived from N-arylglycines using in situ generated chloromethyllithium. The use of the Weinreb amides is essential and allows the chemoselective homologation of N-aryl-N-substituted glycine analogues, a transformation which is not possible using similar glycine esters. The procedure is promising for the large-scale preparation of α-amino-α′-chloropropanones, which are valuable precursors for a variety of bioactive compounds. Copyright

ACETOLYSIS OF α'-SULPHONAMIDO α-CHLORO AND α-DIAZO KETONES. A CONVENIENT SYNTHESIS OF 3-AZETIDINONES

Pusino, Alba,Saba, Antonio,Desole, Giuseppe,Rosnati, Vittorio

, p. 33 - 36 (2007/10/02)

Acetolysis of tertiary sulfonyl amides 1b,d leads to chlorine cinesubstitution exclusively, while in the case of the secondary amides 1a,c,e, only products of β-elimination are obtained.Acetolysis of the related diazo ketones 2b,d bearing a tertiary nitrogen atom, leads to normal substitution of the diazo group exclusively, whereas with the corresponding secondary amides 2a,c,e a concurrent cyclization to the 3-azetidinones 9, 12 and 15 is observed.By decomposition of the same diazoketones 2a,c,e in the presence of catalytic amounts of Cu(CF3COCHCOCF3)2, the above 3-azetidinones are obtained in excellent yields.

Antitumor agents: diazomethyl ketone and chloromethyl ketone analogues prepared from N-tosyl amino acids

Sajadi,Kashani,Loeffler,Hall

, p. 275 - 278 (2007/10/02)

Diazomethyl ketone and chloromethyl ketone analogues prepared from N-tosyl amino acids have been synthesized and tested for antitumor activity in Ehrlich ascites carcinoma and P-388 lymphocytic leukemia screens in mice. The N-tosyl chloromethyl ketone ana

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