60314-07-0

Basic information

• Product Name: 2-methoxy-6-methoxycarbonylbenzoic acid
• Synonyms: 2-methoxy-6-methoxycarbonylbenzoic acid
• CAS NO: 60314-07-0
• Molecular Weight: 210.186
• Mol File: 60314-07-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-methoxy-6-methoxycarbonylbenzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methoxy-6-methoxycarbonylbenzoic acid(60314-07-0)
• EPA Substance Registry System: 2-methoxy-6-methoxycarbonylbenzoic acid(60314-07-0)

Safety Data

• Hazardous Substances Data: 60314-07-0(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 14963-97-4 3-methoxyphthalic acid 
• 32136-52-0 dimethyl 3-methoxyphthalate 

Downstream Products

• 121364-88-3 3-(2,5-dimethoxyphenyl)-3-hydroxy-4-methoxy-1(3H)-isobenzofuranone 
• 121364-89-4 2-<2,5-dimethoxybenzyl>-3-methoxybenzoic acid 
• 83344-25-6 2-Acetyl-5-(2-carbomethoxy-6-methoxybenzoyloxy)-1,2,3,4-tetrahydronaphthalene 
• 97006-25-2 2-Acetyl-5-hydroxy-6-(2-carboxy-6-methoxybenzoyl)-1,2,3,4-tetrahydronaphthalene 
• 97006-24-1 2-Acetyl-5-hydroxy-6-(2-carbomethoxy-6-methoxybenzoyl)-1,2,3,4-tetrahydronaphthalene 
• 78772-96-0 2-(6-Ethyl-1-hydroxy-5,6,7,8-tetrahydro-naphthalene-2-carbonyl)-3-methoxy-benzoic acid 
• 78772-95-9 2-(6-Ethyl-1-hydroxy-5,6,7,8-tetrahydro-naphthalene-2-carbonyl)-3-methoxy-benzoic acid methyl ester 
• 60695-85-4 2-Carbomethoxy-6-methoxy-benzoyl chloride 
• 78772-93-7 3-Methoxy-phthalic acid 2-(6-ethyl-5,6,7,8-tetrahydro-naphthalen-1-yl) ester 1-methyl ester 

Relevant articles and documents

Process for producing rhein and diacerhein

The following description sets forth a process for producing rhein, diacerhein and other diacyl derivatives thereof, which comprises the following steps: treatment of a diphenylketone STR1 in which R1 is --OR', --NR'R", --SR', where R' and R" are H, an alkyl or aromatic group; R2 is H or a protective group, R3 is --OH or C1 -C4 alkyl, with an acid or superacid to give a 1-aminoanthraquinone derivative, diazotisation, replacement of the --NH2 group by --OH, optional removal of the protective group, and acylation.

Facile Interconversion of the Isomeric Acid Chlorides Derived from Half Methyl Esters of 3-Methoxyphthalic Acid

The isomeric acid chlorides obtained by treating the half methyl esters of 3-methoxyphthalic acid with thionyl chloride interconvert so readily that it is not practical to isolate one acid chloride free of the other.At equilibrium the main isomer is the a