80003-86-7

Basic information

• Product Name: Benzoic acid, 3,4-dihydroxy-, phenylMethyl ester
• Synonyms: Benzoic acid, 3,4-dihydroxy-, phenylMethyl ester
• CAS NO: 80003-86-7
• Molecular Formula: C₁₄H₁₂O₄
• Molecular Weight: 244.24268
• Mol File: 80003-86-7.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzoic acid, 3,4-dihydroxy-, phenylMethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 3,4-dihydroxy-, phenylMethyl ester(80003-86-7)
• EPA Substance Registry System: Benzoic acid, 3,4-dihydroxy-, phenylMethyl ester(80003-86-7)

Safety Data

• Hazardous Substances Data: 80003-86-7(Hazardous Substances Data)

Upstream product

• 99-50-3 3,4-Dihydroxybenzoic acid 
• 100-51-6 benzyl alcohol 
• 100-39-0 benzyl bromide 
• 144-55-8 sodium hydrogencarbonate 

Downstream Products

• 953037-17-7 5-carboxy-2-hydroxyphenyl-β-D-glucopyranosiduronic acid 
• 121379-64-4 4-carboxy-2-hydroxyphenyl-β-D-glucopyranosiduronic acid 
• 1376575-40-4 3-hydroxy-4-sulfooxybenzoic acid monoammonium salt 
• 1376575-16-4 benzyl 3-hydroxy-4-(2,2,2-trichloroethoxysulfonyloxy)benzoate 

Relevant articles and documents

SUBSTITUTED PYRIDINE CARBOXYLIC ACIDS, THEIR PREPARATION METHOD AND COMPOSITIONS THEREOF

The present invention relates to novel substituted pyridine carboxylic acid derivatives and their preparation methods. This invention is also directed to pharmaceutical compositions containing such compounds and combinations thereof with at least one ther

Flavonoid metabolism: The synthesis of phenolic glucuronides and sulfates as candidate metabolites for bioactivity studies of dietary flavonoids

Epidemiological studies indicate that flavonoid intake is inversely associated with the risk of coronary heart disease, yet the mechanisms responsible for their bioactivity are still a matter of debate. Based on the rapid and extensive metabolism of most flavonoids, their health effects most likely result from the biological activity of their metabolites. However, a lack of commercially available compounds/standards has prevented the study of metabolite bioactivity and resulted in a focus on non-physiologically relevant precursor/parent structures. This paper details the synthesis of a series of phenolic glucuronide 1a-e and sulfate 2a-e derivates as candidate metabolites for use as reference compounds in metabolic profiling studies and for the exploration of flavonoid bioactivity.

Thermosensitive recording material and color developer compound therefor

A thermosensitive recording material has a support and a thermosensitive coloring layer formed thereon containing a leuco dye and a color developer capable of inducing color formation in the leuco dye upon application of heat thereto, with the color developer including at least one compound (A) having in a molecule thereof at least two aromatic ring moieties with specific structures, selected from the group consisting of an aromatic ring moiety having at least one carboxyl group and electron-attracting functional group, an aromatic ring moiety having at least one carboxyl group and electron-donating functional group, and an aromatic ring moiety having at least one carboxyl group, free of the electron-attracting and electron-donating functional groups. An aromatic carboxylic acid compound serving as the above-mentioned compound (A) and the producing method thereof are also disclosed.