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Phenol, 4-(1-methyl-1-phenylethyl)-, carbonate (2:1) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

33524-49-1

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33524-49-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33524-49-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,5,2 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 33524-49:
(7*3)+(6*3)+(5*5)+(4*2)+(3*4)+(2*4)+(1*9)=101
101 % 10 = 1
So 33524-49-1 is a valid CAS Registry Number.

33524-49-1SDS

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 carbonic acid,4-(2-phenylpropan-2-yl)phenol

1.2 Other means of identification

Product number -
Other names di-PCP carbonate

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:33524-49-1 SDS

33524-49-1Downstream Products

33524-49-1Relevant academic research and scientific papers

Method for Making Carbonates and Esters

-

Page/Page column 7, (2010/06/13)

A method for forming a monomeric carbonate includes the step of combining a monofunctional alcohol or a difunctional diol with an ester-substituted diaryl carbonate to form a reaction mixture. Similarly, a method for forming a monomeric ester includes the step of combining a monofunctional carboxylic acid or ester with an ester-substituted diaryl carbonate to form a reaction mixture. These methods further include the step of allowing the reaction mixtures to react to form a monomeric carbonate or a monomeric ester, respectively.

NOVEL CATALYSIS OF o-NITROPHENYL CARBONATES BY p-DIMETHYLAMINOPYRIDINE

Brunelle, Daniel J.

, p. 1739 - 1742 (2007/10/02)

Transesterification reactions of o-nitrophenyl carbonates have been found to be greatly facilitated by use of p-dialkylaminopyridines as catalysts.A 20-fold rate increase is observed using 0.01 eq. of p-dimethylaminopyridine in place of 2.00 eq. of triethylamine.Such rate enhancement is not observed with p-nitrophenyl carbonates: 2.00 eq. of Et3N causes reaction to occur 8.5 times faster than 0.01 eq. of DMAP.DMAP catalyzed reactions of o-nitrophenyl carbonate have been used to prepare aromatic carbonates at 0 deg C in high yields, and avoid the necessity of using 2 equiv. of base.

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