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35158-23-7

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35158-23-7 Usage

Preparation

Preparation by reaction of ethyl acetoacetate with 5-methyl-2-isopropyl-2-hexenal in the presence of pyridine and piperidine as catalysts in refluxing benzene (40%). The 5-methyl-2-isopropyl-2- hexenal was obtained by self-condensation of isovaleraldehyde in the presence of 15% potassium hydroxide solution.

Check Digit Verification of cas no

The CAS Registry Mumber 35158-23-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,1,5 and 8 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 35158-23:
(7*3)+(6*5)+(5*1)+(4*5)+(3*8)+(2*2)+(1*3)=107
107 % 10 = 7
So 35158-23-7 is a valid CAS Registry Number.

35158-23-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[2-hydroxy-3,5-di(propan-2-yl)phenyl]ethanone

1.2 Other means of identification

Product number -
Other names 3,5-Diisopropyl-2-hydroxyacetophenone

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:35158-23-7 SDS

35158-23-7Downstream Products

35158-23-7Relevant articles and documents

Survivin inhibitors

-

Page/Page column 22, (2010/11/26)

Compounds that inhibit survivin, compositions containing the compounds and methods of treating diseases in which survivin is unregulated or overexpressed are disclosed.

Novel (2E,4E,6Z)-7-(2-alkoxy-3,5-dialkylbenzene)-3-methylocta-2,4,6-trienoic acid retinoid X receptor modulators are active in models of type 2 diabetes

Michellys,Ardecky,Chen,Crombie,Etgen,Faul,Faulkner,Grese,Heyman,Karanewsky,Klausing,Leibowitz,Liu,Mais,Mapes,Marschke,Reifel-Miller,Ogilvie,Rungta,Thompson,Tyhonas,Boehm

, p. 2683 - 2696 (2007/10/03)

Previous data have shown that RXR-selective agonists (e.g., 3 and 4) are insulin sensitizers in rodent models of non-insulin-dependent diabetes mellitus (NIDDM). Unfortunately, they also produce dramatic increases in triglycerides and profound suppression

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