177531-95-2

Basic information

• Product Name: Benzenemethanol, 2-amino-6-methoxy- (9CI)
• Synonyms: Benzenemethanol, 2-amino-6-methoxy- (9CI);(2-Amino-6-methoxyphenyl)methanol
• CAS NO: 177531-95-2
• Molecular Formula: C₈H₁₁NO₂
• Molecular Weight: 153.17844
• Product Categories: METHOXY
• Mol File: 177531-95-2.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzenemethanol, 2-amino-6-methoxy- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, 2-amino-6-methoxy- (9CI)(177531-95-2)
• EPA Substance Registry System: Benzenemethanol, 2-amino-6-methoxy- (9CI)(177531-95-2)

Safety Data

• Hazardous Substances Data: 177531-95-2(Hazardous Substances Data)

Usage

Class

Aromatic compounds

Components

Benzene ring, amino group, methoxy group

Applications

Pharmaceutical, agrochemical, industrial

Potential effects

Human health and environmental impact should be carefully evaluated before use

Upstream product

• 53600-33-2 6-methoxyanthranilic acid 

Downstream Products

• 151585-95-4 2-amino-6-methoxybenzaldehyde 
• 335672-28-1 tert-butyl N-(2-formyl-3-methoxyphenyl)carbamate 

Relevant articles and documents

Construction of a benzo[b]azepine skeleton through decarboxylative ylide [6+1] annulations with modified vinyl benzoxazinanones

A Lewis acid-promoted [6+1] annulation between sulfur ylides and modified vinyl benzoxazinanones was described. In this reaction, the newly designed vinyl benzoxazinanones could serve as a novel six-atom synthon, and the key to success is the installation of an electron-withdrawing group on the alkene moiety of the benzoxazinanones. A broad range of substrates are compatible with this mild reaction system, thereby providing a facile and practical approach for constructing a benzo[b]azepine skeleton.

Palladium-catalyzed oxidative cyclization of aniline-tethered alkylidenecyclopropanes with O2: a facile protocol to selectively synthesize 2- and 3-vinylindoles

A novel palladium-catalyzed oxidative cyclization of aniline-tethered alkylidenecyclopropanes using molecular oxygen as the terminal oxidant through β-carbon elimination of aminopalladation intermediates is disclosed. The reaction opens up an effective way to obtain a series of 2- and 3-vinylindoles which are important synthetic intermediates in many natural indole derivatives.

DIHYDROQUINAZOLINONE ANALOGUES

The present invention encompasses compounds of general formula (I) wherein the groups R1 to R4 and A1 to A5 have the meanings given in the claims and in the specification. The compounds of the invention are suitable for the treatment of diseases characterized by excessive or abnormal cell proliferation pharmaceutical preparations containing such compounds and their uses as a medicament.