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31684-63-6

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31684-63-6 Usage

General Description

The chemical "(4-amino-3-hydroxyphenyl)(phenyl)methanone" is an organic compound that belongs to the class of benzophenones. It is composed of a benzoyl group attached to a phenyl ring, which is further linked to an amino group and a hydroxy group. (4-amino-3-hydroxyphenyl)(phenyl)methanone is often used as a building block in the synthesis of various pharmaceuticals, particularly those that have antibacterial, anti-inflammatory, or anticancer properties. It has also been studied for its potential use as a sunscreen ingredient due to its ability to absorb UV radiation. "(4-amino-3-hydroxyphenyl)(phenyl)methanone" has been the subject of research to explore its potential applications in medicine, materials science, and other industries.

Check Digit Verification of cas no

The CAS Registry Mumber 31684-63-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,6,8 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 31684-63:
(7*3)+(6*1)+(5*6)+(4*8)+(3*4)+(2*6)+(1*3)=116
116 % 10 = 6
So 31684-63-6 is a valid CAS Registry Number.

31684-63-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-amino-3-hydroxyphenyl)-phenylmethanone

1.2 Other means of identification

Product number -
Other names 3-Hydroxy-4-aminobenzophenone

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:31684-63-6 SDS

31684-63-6Relevant articles and documents

On the reaction of Meldrum's acid with N- trimethylsilylanilines substituted by electron withdrawing groups

Roche, Sandrine,Yous, Said,Couturier, Daniel,Rigo, Benoit

, p. 1073 - 1075 (2007/10/03)

The reaction of Meldrum's acid with silylated anilines substituted by an electron withdrawing group easily yields the corresponding N-phenyl malonamic acid, when the reaction is performed under high vacuum in dichlorobenzene.

Unequivocal Preparation of 4- and 5-Acyl-2-aminophenols

Aichaoui, Hocine,Lesieur, Isabelle,Henichart, Jean-Pierre

, p. 679 - 680 (2007/10/02)

Unequivocal methods for the specific preparation of 4- or 5-acyl-2-aminophenols are reported. 5-Acyl-2-aminophenols are obtained by ring opening with dilute sodium hydroxide of 2(3H)-benzoxazolinones acylated at position 6. 4-Acyl-2-aminophenols are obtai

Amides and amines with analgesic and anti-inflammatory activity.

Artini,Buttinoni,Dradi,Logemann,Mandelli,Melloni,Tommasini,Tosolini,Vita

, p. 30 - 36 (2007/10/05)

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