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Benzene, (1-methyl-2-methylenecyclopropyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

105486-60-0

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105486-60-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105486-60-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,4,8 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 105486-60:
(8*1)+(7*0)+(6*5)+(5*4)+(4*8)+(3*6)+(2*6)+(1*0)=120
120 % 10 = 0
So 105486-60-0 is a valid CAS Registry Number.

105486-60-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (1-methyl-2-methylidenecyclopropyl)benzene

1.2 Other means of identification

Product number -
Other names 2-methyl-2-phenyl-1-methylidencyclopropane

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:105486-60-0 SDS

105486-60-0Relevant academic research and scientific papers

Cyclopropenylcarbinol derivatives as new versatile intermediates in organic synthesis: Application to the formation of enantiomerically pure alkylidenecyclopropane derivatives

Simaan, Samah,Masarwa, Ahmad,Zohar, Elinor,Stanger, Amnon,Bertus, Philippe,Marek, Ilan

supporting information; experimental part, p. 8449 - 8464 (2010/06/15)

The copper-catalyzed carbomagnesiation (or hydrometalation) reaction of chiral cyclopropenylcarbinol derivatives, obtained by means of a kinetic resolution of secondary allylic alcohols, leads to an easy and straightforward preparation of enantiomerically

Nickel-catalyzed ring-opening hydroacylation of methylenecyclopropanes: Synthesis of γ,δ-unsaturated ketones from aldehydes

Taniguchi, Hiroki,Ohmura, Toshimichi,Suginome, Michinori

, p. 11298 - 11299 (2011/02/28)

(Chemical Equation Presented) A nickel-catalyzed intermolecular hydroacylation of methylenecyclopropanes (MCPs) has been developed. The reaction proceeds with stereospecific cleavage of the proximal C-C bond of the cyclopropane ring to give γ,δ-unsaturate

Luminescence system, method of luminescence, and chemical substance for luminescence

-

Page/Page column 11, (2008/06/13)

An object of the present invention is to provide, inexpensively and safely, a luminescence system, a method of luminescence, and a luminescent substance based on a novel luminescence mechanism that luminesces at high efficiency. The present invention rela

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