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105577-85-3

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105577-85-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105577-85-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,5,7 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 105577-85:
(8*1)+(7*0)+(6*5)+(5*5)+(4*7)+(3*7)+(2*8)+(1*5)=133
133 % 10 = 3
So 105577-85-3 is a valid CAS Registry Number.

105577-85-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[2-(4-prop-2-enoxyphenyl)propan-2-yl]-2-prop-2-enylphenol

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:105577-85-3 SDS

105577-85-3Downstream Products

105577-85-3Relevant articles and documents

Selective O-allylation of bisphenol A: Toward a chloride-free route for epoxy resins

Van Rijn, Jimmy A.,Guijt, Marieke C.,Bouwman, Elisabeth,Drent, Eite

experimental part, p. 207 - 211 (2012/04/23)

The O-allylation of bisphenol A (BPA) has been performed with the most selective catalysts for O-allylation of phenols reported previously. Both the cyclopentadienyl-ruthenium catalysts and the palladium-diphosphine catalysts are capable of selectively performing single and double O-allylation of BPA. An intriguing solvent effect is observed; the choice of the solvent is of key importance for both conversion and selectivity. The use of an excess of diallyl ether as allylating agent results in relatively high yields of the bisallyl ether of bisphenol A, while maintaining the high selectivity for O-allylation.

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