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2-Propen-1-one, 1-(4-hydroxyphenyl)-2-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60644-65-7

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60644-65-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60644-65-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,6,4 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 60644-65:
(7*6)+(6*0)+(5*6)+(4*4)+(3*4)+(2*6)+(1*5)=117
117 % 10 = 7
So 60644-65-7 is a valid CAS Registry Number.

60644-65-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-hydroxyphenyl)-2-methyl-2-propen-1-one

1.2 Other means of identification

Product number -
Other names 2-(p-hydroxyphenyl)-2-methyl-2-propen-1-one

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:60644-65-7 SDS

60644-65-7Relevant academic research and scientific papers

A methylene compound of preparation method and its application (by machine translation)

-

Paragraph 0023-0024; 0031-0032; 0055-0056, (2017/11/16)

The invention discloses a methylene compound of preparation method and its application, relates to the field of organic synthesis, the process comprises: 1) in the presence of a three-valent metal salt catalyst, will arone compound and halogen methyl radical trialkyl ammonium salt dissolved in a solvent, 2) 80 - 130 °C reaction 1 - 4 hours, separated and purified α - the methyl radical is fragrant compounds, the reaction environment pollution is small, substrate and wide range of application. (by machine translation)

Thermal retro-aldol reaction using fluorous ether F-626 as a reaction medium

Fukuyama, Takahide,Kawamoto, Takuji,Okamura, Takahiro,Denichoux, Aurelien,Ryu, Ilhyong

experimental part, p. 2193 - 2196 (2010/10/21)

A high-boiling, fluorous-organic hybrid ether, F-626, was tested for use in thermal retro-aldol reactions and found to be an excellent reaction medium in view of the ease of separation from the product by fluorous/organic biphasic treatment. The recovered F-626 can be readily reused for subsequent runs.

Preparation of trifluoromethylated dihydrocoumarins, indanones, and arylpropanoic acids by tandem superacidic activation of 2-(Trifluoromethyl) acrylic acid with arenes

Prakash, G. K. Surya,Paknia, Farzaneh,Vaghoo, Habiba,Rasul, Golam,Mathew, Thomas,Olah, George A.

supporting information; experimental part, p. 2219 - 2226 (2010/06/15)

Chemical Reaction Reprentation Indanones and coumarins are important intermediates for the convenient synthesis of many pharmaceutical and biologically active compounds. Fluoroorganics play a vital role in the design of very effective therapeutics due to significant enhancenment in their lipophilicity, bioavailability, and fast uptake by the presence of fluorine in these molecules. Herein, we report an efficient one-pot synthesis of trifluoromethylated arylpropanoic acids, indanones, and dihydrocoumarins using Friedel-Crafts alkylation or tandem Friedel-Crafts alkylation-cycloacylation of arenes/phenols with 2-(trifluoromethyl)acrylic acid under superacidic conditions using trifluoromethanesulfonic acid. The results have been rationalized by the structure energy calculations of the involved reaction intermediates using ab initio theoretical methods.

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