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1134-36-7

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1134-36-7 Usage

Uses

2-Amino-4-phenylphenol is suitable as an internal standard to investigate the enzymatic activity of N-hydroxy-N-2-fluorenylacetamide (N-OH-2-FAA), a mammary gland carcinogen in the female Sprague-Dawley rat, by HPLC. It may be used as a chelating agent for metal ions.

General Description

2-Amino-4-phenylphenol is an aminoalcohol derivative. It participates in the synthesis of bisbenzoxazoles.

Check Digit Verification of cas no

The CAS Registry Mumber 1134-36-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,3 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1134-36:
(6*1)+(5*1)+(4*3)+(3*4)+(2*3)+(1*6)=47
47 % 10 = 7
So 1134-36-7 is a valid CAS Registry Number.

1134-36-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Amino-4-phenylphenol

1.2 Other means of identification

Product number -
Other names [1,1‘-Biphenyl]-4-ol, 3-amino-

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:1134-36-7 SDS

1134-36-7Relevant articles and documents

ACLY INHIBITORS AND USES THEREOF

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Paragraph 00545, (2020/06/01)

The present invention provides compounds useful as inhibitors of ATP citrate lyase (ACLY), compositions thereof, and methods of using the same.

NOVEL DXR INHIBITORS FOR ANTIMICROBIAL THERAPY

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Page/Page column 68; 76, (2011/05/05)

The present invention generally concerns particular methods and compositions for antimicrobial therapy. In particuarl embodiments, the compositions target DXR. In specific embodiments, the compositions are electron-deficient heterocyclic rings.

4-Hydroxyquinolone-(2)-azomethine copper complex pigments

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, (2008/06/13)

A compound having the formula STR1 wherein A denotes an optionally substituted aromatic, isocyclic or heterocyclic residue; R is H, an alkyl residue having from 1 to 6 carbon atoms, an aryl residue having from 6 to 10 carbon atoms or an aralkyl residue having from 7 to 10 carbon atoms; Q is H or a methyl group; X and Y are the same or different and each is a non-water solubilizing group, or X and Y together form a fused aromatic ring system; and R1 and R2 are the same or different and each is H or an alkyl radical having from 1 to 22 carbon atoms, and R3 is hydrogen, an alkyl radical having from 1 to 22 carbon atoms or an aryl radical having from 6 to 10 carbon atoms, the alkyl radicals in R1, R2 and R3 being unsubstituted and uninterrupted or being substituted by an OH, NH2 or CN group and/or being interrupted by an ethylenic group or an oxygen, sulphur or nitrogen bridge, or two or all three of R1, R2 and R3 may form, together with the nitrogen atom to which they are attached, a heterocyclic residue, is useful for pigmenting high molecular weight organic material such as a natural or synthetic polymer or copolymer, or a coating composition for application to the surface of an article, or a printing liquid medium to yield shades from greenish yellow to red brown, exhibiting good fastness properties.

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