24812-91-7

Basic information

• Product Name: methyl 3-amino-4-tert-butylbenzoate
• Synonyms: methyl 3-amino-4-tert-butylbenzoate
• CAS NO: 24812-91-7
• Molecular Formula: C₁₂H₁₇NO₂
• Molecular Weight: 207.26888
• Mol File: 24812-91-7.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: methyl 3-amino-4-tert-butylbenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 3-amino-4-tert-butylbenzoate(24812-91-7)
• EPA Substance Registry System: methyl 3-amino-4-tert-butylbenzoate(24812-91-7)

Safety Data

• Hazardous Substances Data: 24812-91-7(Hazardous Substances Data)

Upstream product

• 59719-78-7 4-tert-butyl-3-nitrobenzoic acid 
• 91641-96-2 methyl 4-(tert-butyl)-3-nitrobenzoate 
• 7440-66-6 zinc 

Downstream Products

• 91639-30-4 methyl 4-(tert-butyl)-3-iodobenzoate 

Relevant articles and documents

Palladium-Catalyzed Alkylation with Alkyl Halides by C(sp3)?H Activation

Utilizing halogens as traceless directing goups represents an attractive strategy for C?H functionalization. A two C?H alkylation system, initiated by the oxidative addition of organohalides to Pd0, has been developed. The first reaction involves an intermolecular alkylation of palladacycles to form C(sp3)?C(sp2) bonds followed by C(sp2)?H activation/cyclization to deliver alkylated benzocyclobutenes as the final products. In the second reaction, two C?C bonds are formed by the reaction of palladacycles with CH2Br2, and provides a facile and efficient method for the synthesis of indanes. The alkylated benzocyclobutene products can be transformed into tricyclic hyrocarbons, and the indane derivatives are essential structural motifs in bioactive and odorant molecules.

Amide derivatives having ACAT inhibitory activity, their preparation and their therapeutic and prohylactic use

Compounds of formula (I): STR1 wherein: R1 is alkyl; R2a, R2b, R2c and R2d are the same or different and each is hydrogen, optionally substituted alkyl, --(C=O)--B1 (wherein B1 i