1042978-66-4

Basic information

• Product Name: 2-aMino-5-(benzyloxy)-4-Methoxybenzaldehyde
• Synonyms: 2-aMino-5-(benzyloxy)-4-Methoxybenzaldehyde
• CAS NO: 1042978-66-4
• Molecular Formula: C₁₅H₁₅NO₃
• Molecular Weight: 257.2845
• Mol File: 1042978-66-4.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-aMino-5-(benzyloxy)-4-Methoxybenzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 2-aMino-5-(benzyloxy)-4-Methoxybenzaldehyde(1042978-66-4)
• EPA Substance Registry System: 2-aMino-5-(benzyloxy)-4-Methoxybenzaldehyde(1042978-66-4)

Safety Data

• Hazardous Substances Data: 1042978-66-4(Hazardous Substances Data)

Usage

Chemical Class

Benzaldehydes

Physical State

White to off-white powder

Solubility

Soluble in organic solvents

Main Use 1

Versatile building block in organic synthesis

Main Use 2

Reagent for synthesizing pharmaceutical compounds and other organic molecules

Potential Medical Application

Inhibitor of monoamine oxidase

Medical Potential

Development of medications for neurological disorders and diseases

This compound's properties and applications make it valuable in various fields, particularly in organic chemistry and pharmaceutical research.

Upstream product

• 58662-50-3 2-aldehyde-4-benzyloxy-5-methoxy nitrobenzene 
• 100-44-7 benzyl chloride 
• 621-59-0 isovanillin 
• 6346-05-0 3-benzyloxy-4-methoxybenzaldehyde 
• 100-39-0 benzyl bromide 

Downstream Products

• 1042978-67-5 6-benzyloxy-7-methoxy-2-(phenylthio)methyl-3-quinolinecarboxylic acid ethyl ester 
• 1387641-82-8 6-benzyloxy-7-methoxy-2-oxo-1,2-dihydro-quinoline-3-carboxylic acid methyl ester 
• 1426813-91-3 6-(benzyloxy)-7-methoxy-2-methyl-N-(benzyl)quinoline-3-carboxamide 
• 1427216-11-2 6-(benzyloxy)-7-methoxy-2-methyl-N-(4-methylphenyl)quinoline-3-carboxamide 
• 1426814-47-2 6-benzyloxy-7-methoxy-2-methyl-N-(2-(thiophen-2-yl)ethyl)quinoline-3-carboxamide 
• 1426814-28-9 6-benzyloxy-7-methoxy-2-methyl-N-(tert-butyl)quinoline-3-carboxamide 
• 1426813-87-7 6-benzyloxy-7-methoxy-2-methyl-N-(n-pentyl)quinoline-3-carboxamide 
• 883251-16-9 6-benzyloxy-7-methoxy-2-methylquinoline-3-carboxylic acid 

Relevant articles and documents

Synthesis and Anti-Hepatitis B Virus Evaluation of 7-Methoxy-3-heterocyclic quinolin-6-ols

A series of novel 7-methoxy-3-heterocyclic quinolin-6-ol derivatives were synthesized and evaluated for their anti-hepatitis B virus (HBV) activities and cytotoxicities in the HepG2.2.15 cell line. Five compounds, 14a, 15c, 15e, 16b, and 16f, displayed ex

Facile and efficient oxidation of quinazolines into quinazolin-4(3 H)-ones by peracetic acid

A new approach to synthesize quinazoline-4(3H)-ones was achieved by oxidation of quinazolines using peracetic acid, which possesses some advantages of economic reagents, simplified operation, high efficiency, and environmental friendliness. Application of this method allowed us to synthesize a series of quinazolin-4(3H)-ones with different substituents at 6 and 7 positions in good to excellent yields, including the key intermediates of tyrosine kinase inhibitors such as PD153035, Erlotinib, and Gefitinib. [Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications for the following free supplemental resource(s): Full experimental and spectral details.]

CARBOXYLIC ACID ARYL AMIDES

Compounds of formula and pharmaceutically acceptable salts thereof are described, as well as the pharmaceutical compositions containing said compounds and their pharmaceutically acceptable salts, and the use of said compounds and pharmaceutical compositions for the treatment, control or amelioration of proliferative diseases, including cancer.