28026-96-2

Basic information

• Product Name: 3,5-Dihydroxy-4-methylbenzoic acid
• Synonyms: DIHYDROXY-4-METHYLBENZOIC ACID,3,5-;4-METHYL-3,5-DIHYDROXY BENZOIC ACID;3,5-DIHYDROXY-4-METHYLBENZOIC ACID;3,5-Dihydroxy-4-Methyl Benzoic Acid 4-Methyl-3,5-Dihydroxy Benzoic Acid;3,5-dihydroxy-p-toluic acid;DIHYDROXY-4-METHYLBENZOIC ACID,3,5-(RG);3,5-Dihydroxy-p-toluic acid (COOH=1);Dihydroxy methylbenzoic acid
• CAS NO: 28026-96-2
• Molecular Formula: C₈H₈O₄
• Molecular Weight: 168.15
• Product Categories: Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;Benzoic acid;Organic acids;Acids & Esters;Phenols
• Mol File: 28026-96-2.mol
• Article Data: 5

Chemical Properties

• Melting Point: 267-268 C
• Boiling Point: 422.2 °C at 760 mmHg
• Flash Point: 223.3 °C
• Appearance: /
• Density: 1.46 g/cm³
• Vapor Pressure: 6.99E-08mmHg at 25°C
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: soluble in Methanol
• PKA: 4.13±0.10(Predicted)
• CAS DataBase Reference: 3,5-Dihydroxy-4-methylbenzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-Dihydroxy-4-methylbenzoic acid(28026-96-2)
• EPA Substance Registry System: 3,5-Dihydroxy-4-methylbenzoic acid(28026-96-2)

Safety Data

• Hazard Codes: C,Xi,Xn
• Statements: 36/37/38-36-22
• Safety Statements: 26-36/37/39-36
• Hazardous Substances Data: 28026-96-2(Hazardous Substances Data)

Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 46, p. 5021, 1981 DOI: 10.1021/jo00337a046

InChI:InChI=1/C8H8O4/c1-4-6(9)2-5(8(11)12)3-7(4)10/h2-3,9-10H,1H3,(H,11,12)/p-1

Upstream product

• 7664-93-9 sulfuric acid 
• 99-94-5 p-Toluic acid 
• 855955-51-0 4,6-dimethoxy-5-methyl-benzene-1,2,3-tricarboxylic acid-1-methyl ester 
• 856806-54-7 3-formyl-4,6-dimethoxy-5-methyl-phthalic acid-1-methyl ester 
• 97424-52-7 3,5-dimethoxy-4-methyl-phthalaldehyde 
• 642-27-3 quadrilineatin 
• 79200-80-9 2,6-Dibromo-3,5-dihydroxybenzoic acid 
• 99-10-5 3,5-Dihydroxybenzoic acid 
• 75238-28-7 3,5-disulphonic-4-methyl-benzoic acid 
• 858852-95-6 3-hydroxy-5-methoxy-4-methyl-phthalic acid-anhydride 
• 10034-85-2 hydrogen iodide 
• 79200-81-0 2,6-Dibromo-3,5-dihydroxy-4-<(dimethylamino)methyl>benzoic acid 
• 76447-14-8 4-Methyl-3,5-dioxocyclohexanecarboxylic Acid 
• 706785-03-7 4,6-dimethoxy-5-methyl-benzene-1,2,3-tricarboxylic acid 

Downstream Products

• 75238-29-8 3,5-dihydroxy-4-methylbenzoic acid methyl ester 
• 80368-86-1 1,3,5,7-tetrahydroxy-2,6-dimethyl-anthraquinone 
• 854178-87-3 3,5-dihydroxy-4-methylbenzyl alcohol 
• 76224-26-5 3,5-diacetoxy-4-methyl-benzoic acid 
• 60441-79-4 methyl 3,5-dimethoxy-4-methylbenzoate 
• 61040-81-1 4-methyl-3,5-dimethoxybenzoic acid 
• 117-02-2 rubiadin 
• 80368-74-7 3-hydroxymorindone 
• 76447-15-9 Benzyl 3,5-Bis(benzyloxy)-4-methylbenzoate 
• 69660-38-4 5-Hydroxy-3-methoxy-4-methylbenzoesaeure-methylester 
• 72922-69-1 methyl 3-(benzyloxy)-5-methoxy-4-methylbenzoate 
• 301530-15-4 3-(benzyloxy)-5-methoxy-4-methylbenzaldehyde 
• 301530-16-5 3-benzyloxy-5-methoxy-4-methylstyrene 
• 254966-01-3 methyl 3,5-bis(methoxycarbonylmethoxy)-4-methylbenzoate 

Relevant articles and documents

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COMPOUNDS WITH 7-MEMBER CYCLE AND THE PHARMACEUTICAL USE THEREOF FOR PREVENTING AND TREATING DIABETES AND METABOLISM SYNDROME

The invention discloses a new use of a class of heptacyclic compounds in the preparation of formulations for the prevention and treatment of diabetes and metabolic syndromes; the present invention also discloses a new class of heptacyclic compounds; the present invention also discloses a process for preparing the heptacyclic compounds and a composition containing the same. The heptacyclic compounds of the present invention can be used to effectively preventing or treating diseases such as diabetes and metabolic syndromes.

An Efficient Synthesis of 3,5-Dihydroxy-4-methylbenzoic Acid

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