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4,4'-dihydroxy-3,5-di-(hydroxymethyl)diphenylmethane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

98711-09-2

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98711-09-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98711-09-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,7,1 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 98711-09:
(7*9)+(6*8)+(5*7)+(4*1)+(3*1)+(2*0)+(1*9)=162
162 % 10 = 2
So 98711-09-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H16O4/c16-8-12-6-11(7-13(9-17)15(12)19)5-10-1-3-14(18)4-2-10/h1-4,6-7,16-19H,5,8-9H2

98711-09-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-Hydroxybenzyl)-2,6-bis(hydroxymethyl)phenol

1.2 Other means of identification

Product number -
Other names -

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:98711-09-2 SDS

98711-09-2Downstream Products

98711-09-2Relevant academic research and scientific papers

Synthesis of new benzylic di-, tri-, and tetraphosphonic acids as potential chelating agents

Aliouane, Nabila,Helesbeux, Jean-Jacques,Douadi, Tahar,Khan, Mustayeen A.,Bouet, Gilles,Chafaa, Salah,Duval, Olivier

experimental part, p. 354 - 364 (2011/04/24)

Chemical Equation Presented New di-, tri-, and tetraphosphonic acids were synthesized starting from four o-hydroxymethyl phenol derivatives and obtained in three steps in good overall yield. The phosphonic acids were isolated and purified using semi-preparative C18 HPLC column. The new compounds were characterized using different spectroscopic methods (1H, 13C, and 31P NMR; ESI MS; and MSn, IR). Copyright Taylor & Francis Group, LLC.

Spectral assignments and reference data: A 13C NMR study of the methylol derivatives of 2,4′- and 4,4′-dihydroxydiphenylmethanes found in resol phenol-formaldehyde resins

Fisher, Thomas H.,Chao, Ping,Upton, Cindy G.,Day, Anthony J.

, p. 747 - 751 (2007/10/03)

A total of 13 of the 16 possible methylol derivatives of 2,4′- and 4,4′-dihydroxydiphenylmethane have been synthesized, isolated, and identified. These compounds are found as intermediates in the cure process of resol phenol-formaldehyde (PF) resins. Analysis of the 13C NMR spectra (in acetone-d6) of these compounds provided a way to evaluate the seven methylolphenol ring types (methylol derivatives of 2-hydroxyphenyl and 4-hydroxyphenyl rings) found in typical resol PF resins using the ipso carbon region from 150 to 160 ppm. A simple diagnostic test was developed using the chemical shift values of the methylol methylene carbon atoms to identify the presence of intermediates containing either a 2-hydroxyphenyl or a 4-hydroxyphenyl ring. Using these data it is now possible to analyze the major components in extracted prepreg PF resins. Copyright

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