37991-83-6

Basic information

• Product Name: 4-(phenylsulfonyl)benzoyl chloride
• Synonyms: 4-(phenylsulfonyl)benzoyl chloride
• CAS NO: 37991-83-6
• Molecular Weight: 280.732
• Mol File: 37991-83-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4-(phenylsulfonyl)benzoyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(phenylsulfonyl)benzoyl chloride(37991-83-6)
• EPA Substance Registry System: 4-(phenylsulfonyl)benzoyl chloride(37991-83-6)

Safety Data

• Hazardous Substances Data: 37991-83-6(Hazardous Substances Data)

Upstream product

• 28525-13-5 4-(phenylsulfonyl)benzonitrile 
• 873-55-2 sodium benzenesulfonate 
• 1194-02-1 4-fluorobenzonitrile 
• 5361-54-6 4-(phenylsulfonyl)benzoic acid 

Downstream Products

• 103167-58-4 bis-(4-benzenesulfonyl-phenyl)-[1,2,4]oxadiazole 
• 66-39-7 4-(phenylsulfonyl)benzaldehyde 
• 618462-01-4 4-benzenesulfonylhippuric acid 
• 20721-07-7 p-(Phenylsulphonyl) benzoic acid hydrazide 
• 1363155-27-4 N-(imidazo[1,2-a]pyridin-6-ylmethyl)-4-(phenylsulfonyl)benzamide 
• 7705-65-9 2-(4-Benzenesulfonyl-benzyl)-2,3-bis-(4-benzenesulfonyl-phenyl)-propionitrile 
• 7705-67-1 2,3-Bis-<4-benzolsulfonyl-phenyl>-propionsaeure-methylester 
• 7705-66-0 4-Benzolsulfonyl-phenylessigsaeure-methylester 
• 7721-90-6 (4-benzenesulfonyl-phenyl)-acetic acid 
• 7705-63-7 1-(bromomethyl)-4-(phenylsulfonyl)benzene 
• 7705-68-2 (4-(phenylsulfonyl)phenyl)methyl methyl ether 
• 7718-66-3 4-Benzolsulfonyl-benzyljodid 
• 618462-06-9 2-aza-1-(4-benzenesulfonylphenyl)-4-mesityl-1,4-butanedione 

Relevant articles and documents

KDM1A INHIBITORS FOR THE TREATMENT OF DISEASE

Disclosed herein are new compounds and compositions and their application as pharmaceuticals for the treatment of diseases. Methods of inhibition of KDM1A, methods of increasing gamma globin gene expression, and methods to induce differentiation of cancer cells in a human or animal subject are also provided for the treatment of diseases such as acute myelogenous leukemia.

Flow-vacuum pyrolysis of polycyclic compounds. 251. Pyrolysis of some 3-mercapto-5-substituted-1,2,4-triazoles

The flow-vacuum pyrolysis (FVP) of the 3-mercapto-5-substituted-1,2,4- triazoles 5a-c, between 475°C - 750°C, at 2 mm Hg, in inert atmosphere (4mL/min argon flow rate) and quartz pyrolysis tube (60 cm length, 1 cm internal diameter, quartz chips filling 30 mm long) afforded a complex mixture with cyano-diphenyl-sulphones 12a-c and corresponding diphenylsulphones 13a-c as main products. The reaction products were identified by GC/MS. A radical mechanism is suggested in order to explain the formation of the main reaction products.