1256493-72-7

Basic information

• Product Name: tert-butyl 3-(2-(4-methylphenylsulfonamido)phenyl)-3-oxopropanoate
• Synonyms: tert-butyl 3-(2-(4-methylphenylsulfonamido)phenyl)-3-oxopropanoate
• CAS NO: 1256493-72-7
• Molecular Weight: 389.472
• Mol File: 1256493-72-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: tert-butyl 3-(2-(4-methylphenylsulfonamido)phenyl)-3-oxopropanoate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl 3-(2-(4-methylphenylsulfonamido)phenyl)-3-oxopropanoate(1256493-72-7)
• EPA Substance Registry System: tert-butyl 3-(2-(4-methylphenylsulfonamido)phenyl)-3-oxopropanoate(1256493-72-7)

Safety Data

• Hazardous Substances Data: 1256493-72-7(Hazardous Substances Data)

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 134-20-3 2-carbomethoxyaniline 
• 540-88-5 acetic acid tert-butyl ester 
• 50998-74-8 methyl N-tosylanthranilate 

Downstream Products

• 1256493-46-5 (Z)-tert-butyl 2-(2-(4-methylphenylsulfonamido)benzoyl)-3-p-tolylacrylate 
• 1256493-45-4 (Z)-tert-butyl 3-(4-chlorophenyl)-2-(2-(4-methylphenylsulfonamido)benzoyl)acrylate 
• 1256493-41-0 (Z)-tert-butyl 2-(2-(4-methylphenylsulfonamido)benzoyl)-3-phenylacrylate 
• 1256493-48-7 (Z)-tert-butyl 3-(4-bromophenyl)-2-(2-(4-methylphenylsulfonamido)benzoyl)acrylate 
• 1256493-52-3 (Z)-tert-butyl 2-(2-(4-methylphenylsulfonamido)benzoyl)-3-(naphthalen-2-yl)acrylate 
• 1256493-53-4 (Z)-tert-butyl 4-methyl-2-(2-(4-methylphenylsulfonamido)benzoyl)pent-2-enoate 
• 1256493-51-2 (Z)-tert-butyl 2-(2-(4-methylphenylsulfonamido)benzoyl)-3-o-tolylacrylate 
• 1256493-50-1 (Z)-tert-butyl 3-(4-ethylphenyl)-2-(2-(4-methylphenylsulfonamido)benzoyl)acrylate 
• 1256493-47-6 (Z)-tert-butyl 2-(2-(4-methylphenylsulfonamido)benzoyl)-3-m-tolylacrylate 
• 1256493-49-8 (Z)-tert-butyl 3-(3-fluorophenyl)-2-(2-(4-methylphenylsulfonamido)benzoyl)acrylate 

Relevant articles and documents

Stereoselective synthesis of fluorinated 2,3-dihydroquinolin-4(1 H)-ones via a one-pot multistep transformation

A new organocatalytic one-pot multistep transformation via Knoevenagel condensation/aza-Michael addition/electrophilic fluorination has been developed. Simple starting materials were used under mild conditions to construct fluorinated 2,3-dihydroquinolin-