6512-25-0

Basic information

• Product Name: dimethyl 2,4-dihydroxy-6-(2-methoxy-2-oxoethyl)benzene-1,3-dicarboxylate
• Synonyms: 1,3-benzenedicarboxylic acid, 2,4-dihydroxy-6-(2-methoxy-2-oxoethyl)-, dimethyl ester; 2,4-Dihydroxy-6-methoxycarbonylmethyl-isophthalic acid dimethyl ester; Dimethyl 2,4-dihydroxy-6-(2-methoxy-2-oxoethyl)isophthalate; Phenylacetic acid, 2,4-dimethoxycarbonyl-3,5-dihydroxy-, methyl ester
• CAS NO: 6512-25-0
• Molecular Formula: C₁₃H₁₄O₈
• Molecular Weight: 298.2455
• Mol File: 6512-25-0.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 421.6°C at 760 mmHg
• Flash Point: 155.4°C
• Density: 1.387g/cm³
• Vapor Pressure: 1.05E-07mmHg at 25°C
• Refractive Index: 1.56
• CAS DataBase Reference: dimethyl 2,4-dihydroxy-6-(2-methoxy-2-oxoethyl)benzene-1,3-dicarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: dimethyl 2,4-dihydroxy-6-(2-methoxy-2-oxoethyl)benzene-1,3-dicarboxylate(6512-25-0)
• EPA Substance Registry System: dimethyl 2,4-dihydroxy-6-(2-methoxy-2-oxoethyl)benzene-1,3-dicarboxylate(6512-25-0)

Safety Data

• Hazardous Substances Data: 6512-25-0(Hazardous Substances Data)

Upstream product

• 1830-54-2 3-oxopentanedioic acid dimethyl ester 
• 100813-80-7 3-(Aminomethylen)-3,4-dihydro-1,2-benzoxathiin-4-on-2,2-dioxid 
• 17094-36-9 dimethyl acetylmalonate 

Downstream Products

• 4670-09-1 2-(3,5-dihydroxyphenyl)acetic acid 
• 4724-10-1 methyl 2-(3,5-dihydroxyphenyl)acetate 
• 4721-07-7 oxyresveratrol 
• 124793-01-7 methyl 3,5-diacetoxy-2-acetyl-4-methoxycarbonylphenylacetate 
• 124793-02-8 methyl 2-crotonyl-3,5-dihydroxy-4-methoxycarbonylphenylacetate 
• 76008-80-5 4-carboxy-3,5-dimethoxyphenylacetic acid dimethyl ester 
• 124793-00-6 methyl 3,5-dihydroxy-4-methoxycarbonylphenylacetate 
• 15495-31-5 methyl 2-acetyl-3,5-dihydroxy-4-methoxycarbonylphenylacetate 
• 124792-99-0 4-carboxy-3,5-dihydroxyphenylacetic acid 
• 6121-79-5 dimethyl 4-carboxy-3,5-dihydroxyhomophthalate 
• 108724-83-0 4-carboxymethyl-2,6-dihydroxy-isophthalic acid dimethyl ester 

Relevant articles and documents

Xylochemical synthesis and biological evaluation of shancigusin c and bletistrin g

The biological activities of shancigusin C (1) and bletistrin G (2), natural products isolated from orchids, are reported along with their first total syntheses. The total synthesis of shancigusin C (1) was conducted by employing the Perkin reaction to forge the central stilbene core, whereas the synthesis of bletistrin G (2) was achieved by the Wittig olefination followed by several regiose-lective aromatic substitution reactions. Both syntheses were completed by applying only renewable starting materials according to the principles of xylochemistry. The cytotoxic properties of shancigusin C (1) and bletistrin G (2) against tumor cells suggest suitability as a starting point for further structural variation.

1,2- and 1,4-additions of methylene-active compounds to a heterocyclic enaminone

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Reaction of Dimethyl 3-Oxoglutarate with 1,3-Dicarbonyl Compounds

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