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

65693-23-4

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65693-23-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65693-23-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,6,9 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 65693-23:
(7*6)+(6*5)+(5*6)+(4*9)+(3*3)+(2*2)+(1*3)=154
154 % 10 = 4
So 65693-23-4 is a valid CAS Registry Number.

65693-23-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-methylidenecyclopropyl)methoxymethylbenzene

1.2 Other means of identification

Product number -
Other names 2-benzyloxymethyl-1-methylenecyclopropane

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:65693-23-4 SDS

65693-23-4Relevant academic research and scientific papers

Bu2SnIH-promoted proximal bond cleavage of methylenecyclopropanes and successive radical cyclization and/or Pd-catalyzed coupling reaction

Hayashi, Naoki,Hirokawa, Yusuke,Shibata, Ikuya,Yasuda, Makoto,Baba, Akio

, p. 2912 - 2913 (2008/09/20)

The unprecedented regioselective hydrostannation of methylenecyclopropanes to give vinyltins was achieved using dibutyliodotin hydride (Bu2SnIH), which could be applied to intramolecular radical cyclization. Copyright

Preparation of methylene-gem-difluorocyclopropanes and its reactivity as Michael Acceptor

Taguchi, Takeo,Kurishita, Masahito,Shibuya, Akira,Aso, Kifune

, p. 9497 - 9508 (2007/10/03)

Preparation of methylene-gem-difluorocyclopropanes 3 was achieved through the selenoxide elimination reaction derived from gem- difluorocyclopropylmethanols 1, while this method can not be applied to non- fluorinated cyclopropylmethanols. The methylene-gem-difluorocyclopropane 3 showed a high reactivity as a Michael acceptor in the reaction with thiol or amine.

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