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Phenol, 3-(1,1-dimethylethyl)-, acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13189-51-0

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13189-51-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13189-51-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,8 and 9 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13189-51:
(7*1)+(6*3)+(5*1)+(4*8)+(3*9)+(2*5)+(1*1)=100
100 % 10 = 0
So 13189-51-0 is a valid CAS Registry Number.

13189-51-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name acetic acid,3-tert-butylphenol

1.2 Other means of identification

Product number -
Other names 3-t-butylphenyl acetate

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:13189-51-0 SDS

13189-51-0Relevant academic research and scientific papers

Steric control of site selectivity in the Pd-catalyzed C-H acetoxylation of simple arenes

Cook, Amanda K.,Emmert, Marion H.,Sanford, Melanie S.

supporting information, p. 5428 - 5431 (2013/11/19)

This report describes the use of an oxidant and a ligand to control site selectivity in the Pd(OAc)2-catalyzed C-H acetoxylation of simple arenes. The use of MesI(OAc)2 as the terminal oxidant in combination with acridine as the ligand results in primarily sterically controlled selectivity. In contrast, with Pd(OAc)2 as the catalyst and PhI(OAc)2 as the oxidant, electronic effects dominate the selectivity of arene C-H acetoxylation.

Antagonists of the Vanilloid Receptor Subtype 1 (VR1) and Uses Thereof

-

Page/Page column 14, (2008/06/13)

The present invention is directed to compounds of formula (I) wherein variables X1, X2, Y, R1a, R1b, R2a, R2b, A1, A2, A3, and A4 are as defined

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