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2,5-Bis(hydroxymethyl)phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

42934-01-0

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42934-01-0 Usage

Also known as

2,5-Dimethylolphenol

Chemical Class

Phenols

Appearance

Colorless to slightly yellow solid at room temperature

Usage in Production

Resins and adhesives
Plywood, laminates, and other wood products (due to phenol-formaldehyde resins)

Functional Groups

Two hydroxymethyl groups

Applications

Cross-linking agent in manufacturing of phenol-formaldehyde resins
Flame retardant
Curing agent in the production of epoxy resins

Industrial Importance

Crucial role in a wide range of industrial applications

Check Digit Verification of cas no

The CAS Registry Mumber 42934-01-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,9,3 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 42934-01:
(7*4)+(6*2)+(5*9)+(4*3)+(3*4)+(2*0)+(1*1)=110
110 % 10 = 0
So 42934-01-0 is a valid CAS Registry Number.

42934-01-0SDS

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 2,5-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:42934-01-0 SDS

42934-01-0Relevant academic research and scientific papers

Nonproteinogenic Amino Acids, IV. - EPC Synthesis of L-(+)-Forphenicine

Weinges, Klaus,Reinel, Ute,Maurer, Wolfgang,Gaessler, Norbert

, p. 833 - 838 (2007/10/02)

Enantiomerically pure L-(+)-forphenicine (12) is synthesized starting from purchasable 3-methoxybenzaldehyde (1) by the use of (4S,5S)-(+)-5-amino-2,2-dimethyl-4-phenyl-1,3-dioxane (2) as a chiral auxiliary and prussic acid. 12 is identical with the natural product which has been isolated from the culture broth of an Actinomyces species and which is known to be a potent inhibitor of alkaline phosphatase.

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