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1H-Inden-1-one, 2,3-dihydro-2,4,5-trimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

105695-59-8

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105695-59-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105695-59-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,6,9 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 105695-59:
(8*1)+(7*0)+(6*5)+(5*6)+(4*9)+(3*5)+(2*5)+(1*9)=138
138 % 10 = 8
So 105695-59-8 is a valid CAS Registry Number.

105695-59-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5-dimethyl-2-methyl-1-indanone

1.2 Other means of identification

Product number -
Other names 2,4,5-trimethyl-indan-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:105695-59-8 SDS

105695-59-8Downstream Products

105695-59-8Relevant academic research and scientific papers

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.

, p. 2219 - 2226 (2010)

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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