67755-25-3

Basic information

• Product Name: 5-HYDROXY-HOMOPHTHALIC ACID
• Synonyms: 2-(CARBOXYMETHYL)-5-HYDROXYBENZOIC ACID;5-HYDROXY-HOMOPHTHALIC ACID
• CAS NO: 67755-25-3
• Molecular Formula: C₉H₈O₅
• Molecular Weight: 196.157
• Mol File: 67755-25-3.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 5-HYDROXY-HOMOPHTHALIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 5-HYDROXY-HOMOPHTHALIC ACID(67755-25-3)
• EPA Substance Registry System: 5-HYDROXY-HOMOPHTHALIC ACID(67755-25-3)

Safety Data

• Hazardous Substances Data: 67755-25-3(Hazardous Substances Data)

Usage

Properties

Chemical compound
Derivative of homophthalic acid
Metabolite of phthalates
Biomarker of exposure to certain phthalates
Potential health effects

Specific Content

Formed as a metabolite of phthalates
Identified as a biomarker of exposure to certain phthalates
Associated with adverse health outcomes including endocrine disruption and reproductive issues
Being explored as a potential biomarker for certain diseases and conditions
Ongoing research and interest in the fields of environmental health and toxicology

Upstream product

• 22901-69-5 5-amino-2-(carboxymethyl)benzoic acid 
• 586415-12-5 2-(β,β-dichloroethenyl)-5-hydroxybenzoic acid 
• 3898-66-6 2-(carboxymethyl)-5-nitrobenzoic acid 
• 89-51-0 Homophthalic acid 
• 99-06-9 3-Carboxyphenol 
• 82735-26-0 6-hydroxy-3-(trichloromethyl)isobenzofuran-1(3H)-one 
• 2516-96-3 2-chloro-5-nitrobenzoic acid 
• 118-91-2 ortho-chlorobenzoic acid 

Downstream Products

• 52962-25-1 2-(carboxymethyl)-5-methoxybenzoic acid 
• 255376-41-1 5-methoxy-2-methoxycarbonylmethyl-benzoic acid methyl ester 
• 4702-29-8 7-methoxy-1H-isochromene-1,3(4H)-dione 
• 1092801-74-5 2-benzyloxy-7-hydroxyisoquinoline-1,3(2H,4H)-dione 
• 1234693-51-6 C₁₅H₁₂O₄S 
• 1609575-79-2 C₁₃H₁₄O₇ 
• 1383786-67-1 methyl 2-{1-[(benzyloxy)amino]-3-methoxy-1,3-dioxopropan-2-yl}-5-methoxybenzoate 
• 1383786-68-2 methyl 2-(benzyloxy)-7-methoxy-1,3-dioxo-1,2,3,4-tetrahydroisoquinoline-4-carboxylate 
• 1383786-69-3 N-(4-fluorobenzyl)-2-(benzyloxy)-7-methoxy-1,3-dioxo-1,2,3,4-tetrahydroisoquinoline-4-carboxamide 
• 1383785-73-6 N-(4-fluorobenzyl)-2-hydroxy-7-methoxy-1,3-dioxo-1,2,3,4-tetrahydroisoquinoline-4-carboxamide 
• 21640-24-4 methyl 5-hydroxy-2-(2-methoxy-2-oxoethyl)benzoate 
• 99866-02-1 (4-ethoxy-2-carboxy-phenyl)-acetic acid 

Relevant articles and documents

A systematic study on the use of different organocatalytic activation modes for asymmetric conjugated addition reactions of isoindolinones

In this article we describe a series of new asymmetric Michael reactions of carboxylate-3-substituted isoindolinones used as nucleophiles in the synthesis of valuable chiral tetrasubstituted derivatives. It has been shown that the reactivity and enantiose

Total synthesis and anti-viral activities of an extract of radix isatidis

Radix isatidis (Banlangen), a famous traditional Chinese medicine, has been used for thousands of years in China due to its anti-viral activity. Through our research, we inferred that the anti-viral activity of Radix isatidis depended on the water-soluble

Design, synthesis, and biological evaluation of a series of 2-hydroxyisoquinoline-1,3(2H,4H)-diones as dual inhibitors of human immunodeficiency virus type 1 integrase and the reverse transcriptase RNase H domain

We report herein the synthesis of a series of 19 2-hydroxyisoquinoline-1, 3(2H,4H)-dione derivatives variously substituted at position 7 aimed at inhibiting selectively two-metal ion catalytic active sites. The compounds were tested against HIV-1 reverse