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Acetic acid, trifluoro-, 3,3-dimethyl-1-phenylbutyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

136272-24-7

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136272-24-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136272-24-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,2,7 and 2 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 136272-24:
(8*1)+(7*3)+(6*6)+(5*2)+(4*7)+(3*2)+(2*2)+(1*4)=117
117 % 10 = 7
So 136272-24-7 is a valid CAS Registry Number.

136272-24-7SDS

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 3,3-dimethyl-1-phenylbutyl trifluoroacetate

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:136272-24-7 SDS

136272-24-7Downstream Products

136272-24-7Relevant academic research and scientific papers

Organophotoredox-Catalyzed Three-Component Coupling of Heteroatom Nucleophiles, Alkenes, and Aliphatic Redox Active Esters

Shibutani, Shotaro,Nagao, Kazunori,Ohmiya, Hirohisa

, p. 1798 - 1803 (2021)

This manuscript describes a visible-light-mediated organophotoredox catalytic process for vicinal difunctionalization of alkenes using heteroatom nucleophiles and aliphatic redox active esters. A wide range of heteroatom nucleophiles including alcohols, water, carboxylic acids, amides, and halogens can be used for this reaction. This radical relay type reaction allows forging of C(sp3)-C(sp3) with a carbon-centered radical and C(sp3)-heteroatom bonds with a benzyl cation on the vinylarenes with complete regioselectivity in a single step.

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