106107-48-6

Basic information

• Product Name: Benzoic acid, 6-[[(1,1-dimethylethoxy)carbonyl]amino]-2,3-dimethoxy-
• CAS NO: 106107-48-6
• Molecular Formula: C14H19NO6
• Molecular Weight: 297.308
• Mol File: 106107-48-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 6-[[(1,1-dimethylethoxy)carbonyl]amino]-2,3-dimethoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 6-[[(1,1-dimethylethoxy)carbonyl]amino]-2,3-dimethoxy-(106107-48-6)
• EPA Substance Registry System: Benzoic acid, 6-[[(1,1-dimethylethoxy)carbonyl]amino]-2,3-dimethoxy-(106107-48-6)

Safety Data

• Hazardous Substances Data: 106107-48-6(Hazardous Substances Data)

Upstream product

• 124-38-9 carbon dioxide 
• 102421-43-2 N-((1,1-dimethylethyl)oxycarbonyl)-3,4-dimethoxyaniline 
• 109-72-8 n-butyllithium 
• 6315-89-5 3,4-dimethoxyaniline 
• 24424-99-5 di-tert-butyl dicarbonate 

Downstream Products

• 5653-51-0 6-amino-2,3-dimethoxybenzoic acid 
• 1429439-90-6 1-ethyl-5-hydroxy-6-((4-methoxybenzyl)oxy)-4-oxo-1,4-dihydroquinolin-3-carboxylic acid 
• 1429439-91-7 1-ethyl-5-hydroxy-6-((4-methoxybenzyl)oxy)-4-oxo-N-(2-(pyrrolidin-1-yl)ethyl)-1,4-dihydroquinolin-3-carboxamide 
• 1429439-89-3 ethyl 1-ethyl-5-hydroxy-6-((4-methoxybenzyl)oxy)-4-oxo-1,4-dihydroquinolin-3-carboxylate 
• 101460-34-8 (S)-2-amino-3-bromo-N-<(1-ethyl-2-pyrrolidinyl)methyl>-5,6-dimethoxybenzamide 
• 122744-80-3 6-bromo-2-carboxy-3,4-dimethoxy-N-(tert-butoxycarbonyl)aniline 
• 122744-79-0 (S)-6-amino-2,3-dimethoxy-N-<(1-ethyl-2-pyrrolidinyl)methyl>benzamide 

Relevant articles and documents

ANTIBACTERIAL COMPOUNDS

The present Invention relates to cephalosporin antibacterial compounds of Formula (!): corresponding pharmaceutically acceptable salts thereof, corresponding pharmaceutical compositions, compound preparation and treatment methods for bacterial infections, especially those caused by gram-negative bacteria.

Alkyl 2-carboalkoxy-3,4-dialkoxybenzenecarbamates and process for their preparation

A process for the preparation of alkyl 2-carboxy-3,4-dialkoxybenzenecarbamates is described. The carbamates are useful intermediates in the preparation of 8-halo-5,6-dialkoxyquinazoline-2,4-diones. The diones are useful as cardiotonic agents.