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Cyclohexane, 1-ethynyl-5-methyl-2-(1-methylethyl)-1-(2-propenyloxy)-, (2S,5R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

487063-81-0

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487063-81-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 487063-81-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,7,0,6 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 487063-81:
(8*4)+(7*8)+(6*7)+(5*0)+(4*6)+(3*3)+(2*8)+(1*1)=180
180 % 10 = 0
So 487063-81-0 is a valid CAS Registry Number.

487063-81-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,5R)-1-Allyloxy-1-ethynyl-2-isopropyl-5-methyl-cyclohexane

1.2 Other means of identification

Product number -
Other names -

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:487063-81-0 SDS

487063-81-0Downstream Products

487063-81-0Relevant academic research and scientific papers

Modification of Terpenoid Derivatives with Ruthenium Catalysts Generated in situ

Notre, Jerome Le,Bruneau, Christian,Dixneuf, Pierre H.

, p. 3816 - 3820 (2007/10/03)

Terpenoids derivatives containing geminal ethynyl and allyloxy groups are easily prepared from the corresponding ketones and aldehydes. The catalytic system generated in situ from [RuCl2(p-cymene)]2, 1,3-bis(mesityl)imidazolinium chloride and cesium carbonate is able to transform these substrates into a new class of terpenoids via cycloisomerisation of the enyne structure.

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