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3-Isobutyl-5-methyl-2-hexanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

40264-43-5

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40264-43-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40264-43-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,2,6 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 40264-43:
(7*4)+(6*0)+(5*2)+(4*6)+(3*4)+(2*4)+(1*3)=85
85 % 10 = 5
So 40264-43-5 is a valid CAS Registry Number.

40264-43-5SDS

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-methyl-3-(2-methylpropyl)hexan-2-one

1.2 Other means of identification

Product number -
Other names 3-Isobutyl-5-methyl-2-hexanone

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:40264-43-5 SDS

40264-43-5Relevant academic research and scientific papers

Copper(I)-Catalyzed Enantioselective Nucleophilic Borylation of Aliphatic Ketones: Synthesis of Enantioenriched Chiral Tertiary α-Hydroxyboronates

Kubota, Koji,Osaki, Shun,Jin, Mingoo,Ito, Hajime

, p. 6646 - 6650 (2017/05/29)

A new method was developed for the first catalytic enantioselective borylation of aliphatic ketones. A variety of substrates reacted efficiently with bis(pinacolato)diboron in the presence of a copper(I)/chiral N-heterocyclic carbene complex catalyst to furnish optically active tertiary α-hydroxyboronates with moderate to high enantioselectivities (up to 94 % ee). Notably, the product could be converted into the chiral tertiary alcohol derivative using a stereospecific boron functionalization process. The theoretical study of the mechanism for the enantioselectivity is also described.

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