3086-72-4

Basic information

• Product Name: 3,5-DIMETHOXY-4-HYDROXYBENZAMIDE
• Synonyms: 3,5-DIMETHOXY-4-HYDROXYBENZAMIDE;4-HYDROXY-3,5-DIMETHOXYBENZAMIDE;SYRINGAMIDE;SYRINGIC AMIDE;3,5-dimethoxy-4-hydroxy-benzamid
• CAS NO: 3086-72-4
• Molecular Formula: C₉H₁₁NO₄
• Molecular Weight: 197.19
• EINECS: 221-407-1
• Product Categories: Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
• Mol File: 3086-72-4.mol
• Article Data: 1

Chemical Properties

• Melting Point: 184-185 °C(Solv: water (7732-18-5))
• Boiling Point: 302.7 °C at 760 mmHg
• Flash Point: 136.9 °C
• Appearance: /
• Density: 1.276 g/cm³
• Vapor Pressure: 0.000543mmHg at 25°C
• Refractive Index: 1.566
• PKA: 8.67±0.23(Predicted)
• CAS DataBase Reference: 3,5-DIMETHOXY-4-HYDROXYBENZAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-DIMETHOXY-4-HYDROXYBENZAMIDE(3086-72-4)
• EPA Substance Registry System: 3,5-DIMETHOXY-4-HYDROXYBENZAMIDE(3086-72-4)

Safety Data

• Hazardous Substances Data: 3086-72-4(Hazardous Substances Data)

Usage

General Description

3,5-Dimethoxy-4-hydroxybenzamide is a synthetic compound belonging to the class of organic compounds known as dimethoxybenzenes. Its systematic name is 3,5-dimethoxy-4-hydroxybenzamide. Notably, it contains two methoxy groups, a benzene ring, and a hydroxy group, making it rich in oxygen-containing functional groups. The compound is structurally characterized by a benzamide core, which can imply potential bioactivity. The physical features of this compound such as solubility, melting point, boiling point, density, among others, along with its reactivity, are influenced by the presence of these functional groups. However, specific details about its properties or uses are not broadly documented in scientific literature.

InChI:InChI=1/C9H11NO4/c1-13-6-3-5(9(10)12)4-7(14-2)8(6)11/h3-4,11H,1-2H3,(H2,10,12)

Upstream product

• 530-57-4 3,5-dimethoxy-4-hydroxybenzoic acid 

Downstream Products

• 530-55-2 2,6-dimethoxy-p-quinone 

Relevant articles and documents

SUBSTITUTED CONDENSED THIOPHENES AS MODULATORS OF STING

A compound of formula (I), wherein: R1 is selected from (i) H, (ii) C3-6cycloalkyl, (iii) C3-7heterocyclyl optionally substituted with a group selected from: methyl and ester, and (iv) linear or branched C1-4alkyl optionally substituted with a group selected from: alkoxy, amino, amido, acylamido, acyloxy, alkyl carboxyl ester, alkyl carbamoyl, alkyl carbamoyl ester, phenyl, phosphonate ester, C3-7heterocyclyl optionally substituted with a group selected from methyl and oxo, and a naturally occurring amino acid, optionally N-substituted with a group selected from methyl, acetyl and boc; A1 is CRA or N; A2 is CRB or N; A3 is CRC or N; A4 is CRD or N; where no more than two of A1, A2, A3, and A4 may be N; one or two of RA, RB, RC, and RD, (if present) are selected from H, F, Cl, Br, Me, CF3, cyclopropyl, cyano, OMe, OEt, CH2OH, CH2OMe and CH2NMe2; the remainder of RA, RB, RC, and RD, (if present) are H; Y is O, NH or CH2; RY is selected from: (RYA) and (RYB).