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2',6'-DIMETHYL-3-(2,6-DIMETHYLPHENYL)PROPIOPHENONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

898754-88-6

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898754-88-6 Usage

Type

Propiophenone derivative

Structure

Ketone with a phenyl group attached to the carbon chain

Substituents

Two methyl groups at the 2' and 6' positions of the phenyl ring
2,6-dimethylphenyl group attached to the ketone carbon

Common Uses

Production of pharmaceuticals
Fragrances
Organic synthesis

Research Status

Subject to ongoing investigation in the field of chemistry for specific properties and potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 898754-88-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,8,7,5 and 4 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 898754-88:
(8*8)+(7*9)+(6*8)+(5*7)+(4*5)+(3*4)+(2*8)+(1*8)=266
266 % 10 = 6
So 898754-88-6 is a valid CAS Registry Number.
InChI:InChI=1/C19H22O/c1-13-7-5-8-14(2)17(13)11-12-18(20)19-15(3)9-6-10-16(19)4/h5-10H,11-12H2,1-4H3

898754-88-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-bis(2,6-dimethylphenyl)propan-1-one

1.2 Other means of identification

Product number -
Other names 2',6'-dimethyl-3-(2,6-dimethylphenyl)propiophenone

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:898754-88-6 SDS

898754-88-6Downstream Products

898754-88-6Relevant academic research and scientific papers

Nonbifunctional Outer-Sphere Strategy Achieved Highly Active α-Alkylation of Ketones with Alcohols by N-Heterocyclic Carbene Manganese (NHC-Mn)

Lan, Xiao-Bing,Ye, Zongren,Huang, Ming,Liu, Jiahao,Liu, Yan,Ke, Zhuofeng

, p. 8065 - 8070 (2019)

The unusual nonbifunctional outer-sphere strategy was successfully utilized in developing an easily accessible N-heterocyclic carbene manganese (NHC-Mn) system for highly active α-alkylation of ketones with alcohols. This system was efficient for a wide range of ketones and alcohols under mild reaction conditions, and also for the green synthesis of quinoline derivatives. The direct outer-sphere mechanism and the high activity of the present system demonstrate the potential of nonbifunctional outer-sphere strategy in catalyst design for acceptorless dehydrogenative transformations.

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