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Phenol, 2-[[(4-hydroxyphenyl)amino]methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13174-45-3

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13174-45-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13174-45-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,7 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13174-45:
(7*1)+(6*3)+(5*1)+(4*7)+(3*4)+(2*4)+(1*5)=83
83 % 10 = 3
So 13174-45-3 is a valid CAS Registry Number.

13174-45-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(4-hydroxyanilino)methyl]phenol

1.2 Other means of identification

Product number -
Other names 4-hydroxyphenylaminomethyl phenol

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:13174-45-3 SDS

13174-45-3Relevant academic research and scientific papers

A study on the co-reaction of benzoxazine and triazine through a triazine-containing benzoxazine

Lin, Ching Hsuan,Chou, Yu-Chun,Wang, Meng Wei,Jeng, Ru Jong

, p. 17539 - 17545 (2016)

To study the co-reaction of benzoxazine and triazine, a triazine-containing benzoxazine (P-tta) was prepared through nucleophilic substitution of 4-(2H-benzo[e][1,3]oxazin-3(4H)-yl)phenol (P-ap) with 2,4,6-trichloro-1,3,5-triazine. DSC thermograms show th

Synthesis and Characterization of Cyanate Ester Functional Benzoxazine and Its Polymer

Ohashi, Seishi,Kilbane, John,Heyl, Tyler,Ishida, Hatsuo

, p. 8412 - 8417 (2015)

The first benzoxazine incorporating cyanate ester group in its structure has been synthesized. The polymerization process investigated by differential scanning calometry (DSC) exhibits two clearly separated exotherm maxima, corresponding to cyanate ester

Concise synthesis and characterization of unsymmetric 1,3-benzoxazines by tandem reactions

Imran, Muhammad,Kiskan, Baris,Yagci, Yusuf

, p. 4966 - 4969 (2013)

A new synthetic protocol for the preparation of unsymmetric 1,3-bisbenzoxazines using the combination of three-step synthesis and classical one-step benzoxazine synthesis strategies is described. For this purpose, 4-hydroxyphenylaminomethyl phenol (HPAMP)

Synthesis and characterization of ion-imprinted resin for selective removal of UO2(II) ions from aqueous medium

Monier,Alatawi, Raedah A. S.,Abdel-Latif

, p. 306 - 315 (2015)

In this work, uranyl ion-imprinted resin based on 2-(((4-hydroxyphenyl)amino)methyl)phenol was synthesized by condensation polymerization of its uranyl complex in presence of resorcinol and formaldehyde cross-linkers. Numerous instrumental techniques incl

The benzoxazine compounds, its manufacturing method and a benzoxazine resin

-

Paragraph 0054; 0057-0059, (2021/06/03)

The present invention provides a novel benzoxazine compound represented by formula (1), from which a highly heat-resistant cured product can be obtained. The present invention also provides a method for producing a benzoxazine compound, the method includi

Flame retardant containing phosphazene ring structure, preparation method and supercapacitor electrolyte solution

-

Paragraph 0022; 0024, (2017/12/09)

The invention specifically relates to a flame retardant containing a phosphazene ring structure, a preparation method and a supercapacitor electrolyte solution using the flame retardant. The preparation method includes: under nitrogen protection, and unde

Triazacycle-containing benzoxazine and preparation method thereof

-

Paragraph 0032, (2016/12/16)

The invention discloses a triazacycle-containing benzoxazine and a preparation method thereof. The method is easy to implement and high in yield, and solves the problem of storage unstability of benzoxazine and cyanate ester; in addition, by using a hardening reaction of the benzoxazine compound having a triazacycle structure, a thermosetting polymer cured material with excellent properties can be obtained, and the dimensional stability and the thermal stability of the cured material are excellent.

Synthesis of 3,4-dihydro-2H-1,3-benzoxazines by condensation of 2-hydroxyaldehydes and primary amines: Application to the synthesis of hydroxy-substituted and deuterium-labeled compounds

Andreu,Ronda

, p. 2316 - 2329 (2008/09/21)

We report the synthesis of several substituted 3,4-dihydro-2H-1,3- benzoxazines by simple ring closure of 2-hydroxybenzylamines with paraformaldehyde. The facile synthesis of the benzylamine precursors from commercially available salicylaldehyde derivativ

Method of topically treating inflammation

-

, (2008/06/13)

This invention describes a method of treating inflammation in warmblooded animals by topically administering an effective amount of benzylamine and its derivatives.

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