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10152-60-0

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10152-60-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10152-60-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,5 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10152-60:
(7*1)+(6*0)+(5*1)+(4*5)+(3*2)+(2*6)+(1*0)=50
50 % 10 = 0
So 10152-60-0 is a valid CAS Registry Number.

10152-60-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 9-cyclopropylnonanoate

1.2 Other means of identification

Product number -
Other names 9-Cyclopropanyl-nonansaeure-methylester

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:10152-60-0 SDS

10152-60-0Relevant articles and documents

A Novel Cathode Material for Cathodic Dehalogenation of 1,1-Dibromo Cyclopropane Derivatives

Gütz, Christoph,Selt, Maximilian,B?nziger, Markus,Bucher, Christoph,R?melt, Christina,Hecken, Nadine,Gallou, Fabrice,Galv?o, Tomás R.,Waldvogel, Siegfried R.

, p. 13878 - 13882 (2015)

Leaded bronze turned out to be an excellent cathode material for the dehalogenation reaction of cyclopropanes without affecting the strained molecular entity. With this particular alloy, beneficial properties of lead cathodes are conserved, whereas the corrosion of cathode is efficiently suppressed. The solvent in the electrolyte determines whether a complete debromination reaction is achieved or if the process can be selectively stopped at the monobromo cyclopropane intermediate. The electroorganic conversion tolerates a variety of functional groups and can be conducted at rather complex substrates like cyclosporine A. This approach allows the sustainable preparation of cyclopropane derivatives.

Structure-antitumor activity relationship of semi-synthetic spicamycin derivatives

Sakai,Kawai,Kamishohara,Odagawa,Suzuki,Uchida,Kawasaki,Tsuruo,Otake

, p. 1467 - 1480 (2007/10/03)

New derivatives of spicamycin modified at the fatty acid moieties of the molecule were synthesized and their structure-activity relationships were examined. The antitumor activity was greatly influenced by modification of the fatty acid moieties to tetradecadienoyl or dodecadienoyl analogues exhibiting better antitumor activity against COL-1 human colon cancer xenograft than SPM VIII.

Control of mites with esters of cyclopropane substituted carboxylic acids

-

, (2008/06/13)

Esters of cyclopropyl substituted carboxylic acids, syntheses thereof, compositions thereof, and use for the control of mites and ticks.

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