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3-Penten-2-one, 3,4-dimethyl-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67515-48-4

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67515-48-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67515-48-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,5,1 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 67515-48:
(7*6)+(6*7)+(5*5)+(4*1)+(3*5)+(2*4)+(1*8)=144
144 % 10 = 4
So 67515-48-4 is a valid CAS Registry Number.

67515-48-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-dimethyl-1-phenyl-pent-3-en-2-one

1.2 Other means of identification

Product number -
Other names 3,4-Dimethyl-1-phenyl-pent-3-en-2-on

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:67515-48-4 SDS

67515-48-4Downstream Products

67515-48-4Relevant academic research and scientific papers

Method for synthesizing polysubstituted alpha, beta unsaturated ketones

-

Paragraph 0039-0043, (2020/03/06)

The invention particularly relates to a method for synthesizing polysubstituted alpha, beta unsaturated ketones. The method comprises the following steps: 1, adding Ni(cod), an N-heterocyclic carbene ligand, Cs2CO3 and a beta, gamma unsaturated ketone into a non-polar aprotic organic solvent, and mixing to obtain a mixture; 2, adding the mixture obtained in the step 1 into a dried container, reacting for 10-40 hours at the reaction temperature of 120-180 DEG C, and cooling to room temperature after the reaction is finished, so as to obtain a crude product; 3, purifying. According to the method, cheap Ni(cod) is adopted as a catalyst, carbon-carbon bonds are activated by a transition metal, power is provided for the reaction through isomerization of double bonds, the synthesis methodis simple, the substrates are stable and cheap, the reaction is less limited by the substrate, and the substrates are wide in application range.

Ni-Catalyzed 1,2-Acyl Migration Reactions Triggered by C-C Bond Activation of Ketones

Jiang, Cheng,Lu, Hong,Xu, Wen-Hua,Wu, Jianing,Yu, Tian-Yang,Xu, Peng-Fei,Wei, Hao

, p. 1947 - 1953 (2020/02/06)

A Ni-catalyzed 1,2-acyl migration triggered by C-C bond cleavage was developed. The process of 1,2-acyl migration followed by olefin isomerization provides a convenient access to α,β-unsaturated ketones, which are well-known building blocks in organic syn

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