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40430-57-7

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40430-57-7 Usage

General Description

1-Acetyl-3,5-dimethyl adamantane is a chemical compound with the molecular formula C16H24O. It is a derivative of adamantane, a diamondoid hydrocarbon. 1-Acetyl-3,5-dimethyl Adamantane is used as a starting material for the synthesis of new pharmaceutical and agrochemical compounds. Its structure and properties make it a valuable intermediate in the development and production of various potential drugs and pesticides. 1-Acetyl-3,5-dimethyl adamantane has potential applications in the pharmaceutical and agricultural industries due to its unique properties and structure.

Check Digit Verification of cas no

The CAS Registry Mumber 40430-57-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,4,3 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 40430-57:
(7*4)+(6*0)+(5*4)+(4*3)+(3*0)+(2*5)+(1*7)=77
77 % 10 = 7
So 40430-57-7 is a valid CAS Registry Number.

40430-57-7SDS

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 1-Acetyl-3,5-dimethyl Adamantane

1.2 Other means of identification

Product number -
Other names 1-[(3R,5S)-3,5-dimethyl-1-adamantyl]ethanone

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:40430-57-7 SDS

40430-57-7Relevant articles and documents

Enantioselective borohydride reduction of aliphatic ketones catalyzed by ketoiminatocobalt(iii) complex with 1-chlorovinyl axial ligand

Tsubo, Tatsuyuki,Chen, Hsiu-Hui,Yokomori, Minako,Fukui, Kosuke,Kikuchi, Satoshi,Yamada, Tohru

, p. 780 - 782 (2012/09/22)

For the enantioselective borohydride reduction of aliphatic ketones, the optically active ketoiminatocobalt(II) catalysts was successfully designed based on their axial ligand. Instead of chloroform for the aryl ketone reduction, various axial ligand precursors were examined for the aliphatic ketone. Consequently, 1, 1, 1-trichloroethane was found to be the most effective activator of the cobalt(II) complexes to generate the corresponding 1-chlorovinyl cobalt(III) derivatives as the reactive intermediate. Several aliphatic ketones were successfully reduced to afford the corresponding secondary alcohols with high enantioselectivities.

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