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187731-65-3

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187731-65-3 Usage

General Description

2-AMINO-4-METHOXYBENZYL ALCOHOL, also known as 2-amino-4-methoxybenzyl alcohol or 4-methoxy-2-aminobenzyl alcohol, is a chemical compound with the molecular formula C8H11NO2. It is a phenolic compound with a methoxy group and an amino group attached to a benzyl alcohol moiety. 2-AMINO-4-METHOXYBENZYL ALCOHOL has potential applications in various fields, including pharmaceuticals and organic synthesis. It can be used as a building block in the synthesis of various organic compounds and can also be used as a chiral building block in the preparation of chiral ligands for asymmetric synthesis. Additionally, it exhibits antioxidant and antimicrobial properties, making it a potentially useful compound in the development of pharmaceuticals and other products.

Check Digit Verification of cas no

The CAS Registry Mumber 187731-65-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,7,7,3 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 187731-65:
(8*1)+(7*8)+(6*7)+(5*7)+(4*3)+(3*1)+(2*6)+(1*5)=173
173 % 10 = 3
So 187731-65-3 is a valid CAS Registry Number.

187731-65-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-amino-4-methoxyphenyl)methanol

1.2 Other means of identification

Product number -
Other names 2-AMINO-4-METHOXYBENZYL ALCOHOL

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:187731-65-3 SDS

187731-65-3Relevant articles and documents

The role of methoxy substituents in regulating the activity of selenides that serve as spirodioxyselenurane precursors and glutathione peroxidase mimetics

Press, David J.,Back, Thomas G.

, p. 305 - 311 (2016)

A series of o-(hydroxymethyl)phenyl selenides containing single or multiple methoxy substituents was synthesized, and the rate at which each compound catalyzed the oxidation of benzyl thiol to its disulfide with excess hydrogen peroxide was measured. This

Easy Access to Quinolin-2(1 H)-ones via a One-Pot Tandem Oxa-Michael-Aldol Sequence

Jarrige, Lucie,Merad, Jeremy,Zaied, Siwar,Blanchard, Florent,Masson, Géraldine

, p. 1724 - 1728 (2017/10/06)

An efficient strategy for the synthesis of a variety of quinolin-2(1 H)-one derivatives has been developed. The reaction proceeded from cinnamide derivatives via a tandem reaction in the presence of NaOH to afford the corresponding 2- quinolin-2(1 H)-one derivatives in good to excellent yields.

INHIBITORS OF THE FIBROBLAST GROWTH FACTOR RECEPTOR

-

Paragraph 0476; 0477; 0478, (2015/05/05)

Described herein are inhibitors of FGFR-4, pharmaceutical compositions including such compounds, and methods of using such compounds and compositions.

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