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59386-47-9

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59386-47-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59386-47-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,3,8 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 59386-47:
(7*5)+(6*9)+(5*3)+(4*8)+(3*6)+(2*4)+(1*7)=169
169 % 10 = 9
So 59386-47-9 is a valid CAS Registry Number.

59386-47-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-decylcyclohexan-1-one

1.2 Other means of identification

Product number -
Other names 2-decylcyclohexanone

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:59386-47-9 SDS

59386-47-9Relevant articles and documents

Alkylation of magnesium enamide with alkyl chlorides and fluorides

Hatakeyama, Takuji,Ito, Shingo,Nakamura, Masaharu,Nakamura, Eiichi

, p. 14192 - 14193 (2005)

A magnesium enamide derived from N-2-(N′,N′-diethylamino)ethyl imine reacts with a primary and secondary alkyl chloride or a primary alkyl fluoride to give an α-alkylated ketone in good to excellent yield after hydrolysis. The reaction takes place with a high level of inversion of stereochemistry at the electrophilic carbon center and will be useful for production of optically active compounds. Copyright

Enzymatic resolution of bicyclo[n.1.0]alkan-1-ols derivatives: Preparation of optically active α-substituted α-methylcycloalkanones

Morisson,Barnier,Blanco

, p. 7749 - 7764 (2007/10/03)

Optically active α-methyl α-substituted cycloalkanones are prepared by a chemoenzymatic sequence which involves a Lipozyme-catalyzed transesterification of 1-(chloroacetoxy)bicyclo[n.1.0]alkanes and ring opening of these cyclopropanol derivatives.

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