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

102503-95-7

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102503-95-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102503-95-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,5,0 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 102503-95:
(8*1)+(7*0)+(6*2)+(5*5)+(4*0)+(3*3)+(2*9)+(1*5)=77
77 % 10 = 7
So 102503-95-7 is a valid CAS Registry Number.

102503-95-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-<1-Methyl-2-oxo-cyclohexyl-(1)>-pentan-2-on

1.2 Other means of identification

Product number -
Other names 5-(1-Methyl-2-oxo-cyclohexyl-(1))-pentan-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:102503-95-7 SDS

102503-95-7Downstream Products

102503-95-7Relevant academic research and scientific papers

Reductive intramolecular Henry reactions induced by Stryker's reagent

Chung, Wing Ki,Chiu, Pauline

, p. 55 - 58 (2007/10/03)

Conjugate reductions of nitroalkenes by Stryker's reagent are ensued by intramolecular aldol reactions to produce β-nitroalcohols in good yield, constituting the first examples of reductive Henry reactions.

β-CARBONYL RADICALS AS THREE-CARBON BUILDING BLOCKS FOR CARBON-CARBON BOND FORMING REACTIONS

Giese, Bernd,Horler, Hans

, p. 4025 - 4038 (2007/10/02)

From aldehydes, ketones and esters β-carbonyl radicals 47 can be generated via enolization, cyclopropanation, solvomercuration and reduction with NaBH4.Radicals 47 react with electron-poor alkenes 27 to give products of CC-bond forming reactions (Tables 1-3).Carbonyl compounds are therefore precursors of three-carbon building blocks.The products result from reactions with "Umpolung".

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