346725-77-7

Basic information

• Product Name: 4-tert-butyl-N-(3,5-dimethylphenyl)benzamide
• Synonyms: 4-tert-butyl-N-(3,5-dimethylphenyl)benzamide
• CAS NO: 346725-77-7
• Molecular Formula: C19H23NO
• Molecular Weight: 281.39202
• Mol File: 346725-77-7.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-tert-butyl-N-(3,5-dimethylphenyl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-tert-butyl-N-(3,5-dimethylphenyl)benzamide(346725-77-7)
• EPA Substance Registry System: 4-tert-butyl-N-(3,5-dimethylphenyl)benzamide(346725-77-7)

Safety Data

• Hazardous Substances Data: 346725-77-7(Hazardous Substances Data)

Upstream product

• 54132-75-1 3,5-dimethylphenyl isocyanate 
• 203321-89-5 (3,5-dimethylphenyl)carbamic acid 1,1-dimethylethyl ester 
• 123324-71-0 p-tert-butylphenylboronic acid 
• 1370412-35-3 2-(4-(tert-butyl)phenyl)-1,3,2-dioxaborinane 

Relevant articles and documents

Direct Amidation of N-Boc- and N-Cbz-Protected Amines via Rhodium-Catalyzed Coupling of Arylboroxines and Carbamates

N-Boc- and N-Cbz-protected amines are directly converted into amides by a novel rhodium-catalyzed coupling of arylboroxines and carbamates, replacing the traditional two-step deprotection-condensation sequence. Both protected anilines and aliphatic amines are efficiently transformed into a wide variety of secondary benzamides, including sterically hindered and electron-deficient amides, as well as in the presence of acid-labile and reducible functional groups.

Pharmaceutical compositions containing phenylamides

Pharmaceutical compositions for inhibiting the aggregation of erthyrocytes or thrombocytes which include phenylamides which conform to the formula: STR1 with R1-6, X, A and B being as defined. Processes for the preparation of novel phenylamides