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4-Methylbenzophenone-d3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

109339-64-2

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109339-64-2 Usage

Uses

Labelled 4-Methylbenzophenone. Benzophenone estrogenicity toxicity structure activity.

Check Digit Verification of cas no

The CAS Registry Mumber 109339-64-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,3,3 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 109339-64:
(8*1)+(7*0)+(6*9)+(5*3)+(4*3)+(3*9)+(2*6)+(1*4)=132
132 % 10 = 2
So 109339-64-2 is a valid CAS Registry Number.

109339-64-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name phenyl-[4-(trideuteriomethyl)phenyl]methanone

1.2 Other means of identification

Product number -
Other names Phenyl(4-tolyl)methanone-d3

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:109339-64-2 SDS

109339-64-2Relevant academic research and scientific papers

Nickel and Nucleophilic Cobalt-Catalyzed Trideuteriomethylation of Aryl Halides Using Trideuteriomethyl p-Toluenesulfonate

Komeyama, Kimihiro,Yamahata, Yuta,Osaka, Itaru

supporting information, p. 4375 - 4378 (2018/07/29)

Herein, a novel approach for the trideuteriomethylation of aryl halides using nickel and nucleophilic cobalt catalysts and the readily available trideuteriomethyl p-toluenesulfonate (CD3OTs) is described. This method provides access to a wide r

Development of a Rhodium(II)-Catalyzed Chemoselective C(sp3)-H Oxygenation

Lin, Yun,Zhu, Lei,Lan, Yu,Rao, Yu

supporting information, p. 14937 - 14942 (2015/10/19)

We report the first example of RhII-catalyzed chemoselective double C(sp3)-H oxygenation, which can directly transform various toluene derivatives into highly valuable aromatic aldehydes with great chemoselectivity and practicality. The critical combination of catalyst Rh(OAc)2, oxidant Selectfluor, and solvents of TFA/TFAA promises the successful delivery of the oxidation with satisfactory yields. A possible mechanism involving a unique carbene-Rh complex is proposed, and has been supported by both experiments and theoretical calculations.

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