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91793-46-3

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91793-46-3 Usage

Chemical structure

1,3-Bis(4-hydroxyphenyl)-2-propanol

Type of compound

Synthetic organic compound

Usage

Production of plastics and epoxy resins

Common products

Water bottles, food containers, dental sealants, and thermal paper

Health concerns

Potential to leach into foods and beverages

Hormonal activity

Mimics the hormone estrogen in the body

Research findings

Linked to reproductive disorders, developmental delays, and increased risk of certain cancers

Regulatory actions

Many countries have restricted the use of BPA in certain products

Industry response

Growing trend towards the development of BPA-free alternatives

Check Digit Verification of cas no

The CAS Registry Mumber 91793-46-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,7,9 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 91793-46:
(7*9)+(6*1)+(5*7)+(4*9)+(3*3)+(2*4)+(1*6)=163
163 % 10 = 3
So 91793-46-3 is a valid CAS Registry Number.

91793-46-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[2-hydroxy-3-(4-hydroxyphenyl)propyl]phenol

1.2 Other means of identification

Product number -
Other names Propterol

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:91793-46-3 SDS

91793-46-3Relevant articles and documents

Direct α-Benzylation of Methyl Enol Ethers with Activated Benzyl Alcohols: Its Rearrangement and Access to (±)-Tetrahydronyasol, Propterol A, and 1,3-Diarylpropane

Jena, Tapan Kumar,Khan, Faiz Ahmed

, p. 14270 - 14280 (2019)

Herein, we report a one-pot Lewis acid mediated synthesis of bi- and triarylpropanal derivatives and their corresponding isomeric ketones from aromatic enol ethers. This transformation takes place via nucleophilic attack of enol ethers to electron-rich be

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