33927-05-8

Basic information

• Product Name: METHYL 3,5-DINITRO-4-HYDROXYBENZOATE
• Synonyms: METHYL 4-HYDROXY-3,5-DINITROBENZOATE;METHYL 3,5-DINITRO-4-HYDROXYBENZOATE;4-HYDROXY-3,5-DINITROBENZOIC ACID METHYL ESTER;3 5-DINITRO-4-HYDROXYBENZOIC ACID METHYL ESTER;3 5-DINITRO-4-HYDROXYBENZOIC ACID METHYL ESTER 97%;4-HYDROXY-3,5-DINITROBENZOIC ACID METHYL ESTER 97%
• CAS NO: 33927-05-8
• Molecular Formula: C₈H₆N₂O₇
• Molecular Weight: 242.14
• Product Categories: Aromatic Esters
• Mol File: 33927-05-8.mol
• Article Data: 1

Chemical Properties

• Melting Point: 108-110°C
• Boiling Point: 331.8°Cat760mmHg
• Flash Point: 154.5°C
• Appearance: /
• Density: 1.62g/cm³
• Vapor Pressure: 7.89E-05mmHg at 25°C
• Refractive Index: 1.627
• CAS DataBase Reference: METHYL 3,5-DINITRO-4-HYDROXYBENZOATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL 3,5-DINITRO-4-HYDROXYBENZOATE(33927-05-8)
• EPA Substance Registry System: METHYL 3,5-DINITRO-4-HYDROXYBENZOATE(33927-05-8)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 33927-05-8(Hazardous Substances Data)

Usage

Description

METHYL 3,5-DINITRO-4-HYDROXYBENZOATE is an organic compound characterized by its molecular structure featuring a methyl group, two nitro groups, and a hydroxyl group attached to a benzoate backbone. It is known for its potential applications in various fields, particularly due to its chemical properties and reactivity.

Uses

Used in Pharmaceutical Industry:
METHYL 3,5-DINITRO-4-HYDROXYBENZOATE is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows it to be a key component in the development of new drugs with specific therapeutic properties.
Used in Anticancer Applications:
METHYL 3,5-DINITRO-4-HYDROXYBENZOATE is used as an anticancer agent to reduce susceptibility to tumor formation. Its chemical properties enable it to interact with cellular components and potentially inhibit the growth and progression of cancer cells.
Used in Chemical Research:
METHYL 3,5-DINITRO-4-HYDROXYBENZOATE is utilized as a research compound in the field of organic chemistry. Its reactivity and structural features make it a valuable tool for understanding various chemical reactions and mechanisms, which can lead to the discovery of new compounds and applications.

InChI:InChI=1/C8H6N2O7/c1-17-8(12)4-2-5(9(13)14)7(11)6(3-4)10(15)16/h2-3,11H,1H3

Upstream product

• 67-56-1 methanol 
• 1019-52-9 4-hydroxy-3,5-dinitrobenzoic acid 
• 99-76-3 methyl 4-hydroxylbenzoate 
• 7697-37-2 nitric acid 
• 99-96-7 4-hydroxy-benzoic acid 

Downstream Products

• 2552-45-6 methyl 4-chloro-3,5-dinitrobenzoate 
• 1019-52-9 4-hydroxy-3,5-dinitrobenzoic acid 
• 33927-08-1 4-(4-methoxy-phenoxy)-3,5-dinitro-benzoic acid methyl ester 
• 412020-13-4 4-(4-methoxy-phenoxy)-3,5-dinitro-benzoyl chloride 
• 267014-44-8 3-amino-4-hydroxy-5-nitro-benzoic acid 
• 34043-77-1 3,5-diiodo-4-(4-methoxy-phenoxy)-benzoic acid 
• 33927-09-2 methyl 3,5-diiodo-4-(4'-methoxyphenoxy)-benzoate 
• 34043-76-0 3,5-diamino-4-(4-methoxy-phenoxy)-benzoic acid methyl ester 
• 92061-04-6 4-(4-methoxy-phenoxy)-3,5-dinitro-benzoic acid 

Relevant articles and documents

Amino-benzoic acids and derivatives, and methods of use

The present invention relates to compounds, compositions and methods for inhibiting nonenzymatic cross-linking (protein aging). Accordingly, a composition is disclosed which comprises an agent capable of inhibiting the formation of advanced glycosylation endproducts of target proteins by reacting with a carbonyl moiety of the early glycosylation product of such target proteins formed by their initial glycosylation. The method comprises contacting the target protein with the composition. Both industrial and therapeutic applications for the invention are envisioned, as food spoilage and animal protein aging can be treated.