89984-23-6

Basic information

• Product Name: Benzaldehyde, 2-amino-4-hydroxy-3-methoxy-
• Synonyms: Benzaldehyde, 2-amino-4-hydroxy-3-methoxy-;2-Amino-4-hydroxy-3-methoxybenzaldehyde;2-aMino-4-hydroxy-3-Methoxy-
• CAS NO: 89984-23-6
• Molecular Formula: C₈H₉NO₃
• Molecular Weight: 167.16
• Mol File: 89984-23-6.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 341.6°C at 760 mmHg
• Flash Point: 160.4°C
• Appearance: /
• Density: 1.328g/cm³
• Vapor Pressure: 4.03E-05mmHg at 25°C
• Refractive Index: 1.648
• CAS DataBase Reference: Benzaldehyde, 2-amino-4-hydroxy-3-methoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 2-amino-4-hydroxy-3-methoxy-(89984-23-6)
• EPA Substance Registry System: Benzaldehyde, 2-amino-4-hydroxy-3-methoxy-(89984-23-6)

Safety Data

• Hazardous Substances Data: 89984-23-6(Hazardous Substances Data)

Usage

General Description

Benzaldehyde, 2-amino-4-hydroxy-3-methoxy- is a chemical compound with a molecular formula C9H9NO3. It is an aromatic aldehyde that contains a benzene ring with a formyl group attached. The compound also has an amino group and hydroxyl group attached to the benzene ring, as well as a methoxy group at the para position. Benzaldehyde, 2-amino-4-hydroxy-3-methoxy- is used in various industrial processes, including the production of pharmaceuticals, dyes, and perfumes. It also has potential applications in the food industry as a flavoring agent. Additionally, it has been studied for its potential biological activities and has shown promise in various medicinal applications.

InChI:InChI=1/C8H9NO3/c1-12-8-6(11)3-2-5(4-10)7(8)9/h2-4,11H,9H2,1H3

Upstream product

• 2450-26-2 2-nitrovanillin 
• 2698-69-3 4-formyl-2-methoxy-3-nitrophenyl acetate 
• 881-68-5 vanillin acetate 
• 121-33-5 vanillin 

Downstream Products

• 82668-20-0 2-Chlorovanillin 
• 89984-24-7 2-bromo-4-hydroxy-3-methoxy-benzaldehyde 
• 89942-36-9 2-iodo-4-hydroxy-3-methoxybenzaldehyde 
• 499218-04-1 4-(benzyloxy)-2-bromo-3-methoxybenzaldehyde 
• 620167-53-5 2-(4-benzyloxy-2-bromo-3-methoxy-benzyl)-3,3-dimethyl-cyclohexanone 
• 620167-54-6 1-benzyloxy-3-bromo-4-(2,2-dimethyl-6-methylene-cyclohexylmethyl)-2-methoxy-benzene 
• 620167-52-4 2-(4-benzyloxy-2-bromo-3-methoxy-benzyl)-3-methyl-4-oxo-cyclohex-2-enone 
• 859172-24-0 2-iodo-3-methoxy-4-(2-methoxy-ethoxymethoxy)-benzylamine 
• 859171-91-8 [2-iodo-3-methoxy-4-(2-methoxy-ethoxymethoxy)-phenyl]-methanol 
• 859172-25-1 nonanoic acid 2-iodo-3-methoxy-4-(2-methoxy-ethoxymethoxy)-benzylamide 
• 55171-60-3 2-bromo-3,4-dimethoxybenzylaldehyde 
• 71568-87-1 2-bromo-3,4-dimethoxybenzoic acid 
• 92351-94-5 deuterated vanillin 
• 110038-86-3 2-Chloro-4-hydroxy-3-methoxybenzenemethanol 

Relevant articles and documents

BORON-CONTAINING SMALL MOLECULES

Compounds, pharmaceutical formulations, and methods of treating bacterial infections are disclosed.

Electronic control of product distribution in the [5+5]-coupling of ortho-alkynylbenzaldehyde derivatives and γ,δ-unsaturated carbene complexes

The coupling of highly oxygenated ortho-alkynylbenzaldehyde derivatives with γ,δ-carbene complexes was evaluated systematically. In all of the electron-rich systems investigated the exclusive product of the reaction is the dihydrophenanthrene derivative.

General route to 4a-methylhydrofluorene diterpenoids: Total syntheses of (±)-taiwaniaquinones D and H, (±)-taiwaniaquinol B, (±)-dichroanal B, and (±)-dichroanone

A general and convergent route for the synthesis of the 4a-methylhydrofluorene diterpenoids has been established through a common hexahydrofluorenone intermediate (10) obtained via Pd(0)-catalyzed reductive cyclization of a substituted 2-(2-bromobenzyl) methylene cyclohexane (13). The strategy has been successfully utilized for the synthesis of (±)-taiwaniaquinones D (3) and H (5), (±)-taiwaniaquinol B (1), (±)-dichroanal B (7), and (±)-dichroanone (8).