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1-Penten-3-one, 4-[(1R)-4-methyl-3-cyclohexen-1-yl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

629624-72-2

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629624-72-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 629624-72-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,9,6,2 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 629624-72:
(8*6)+(7*2)+(6*9)+(5*6)+(4*2)+(3*4)+(2*7)+(1*2)=182
182 % 10 = 2
So 629624-72-2 is a valid CAS Registry Number.

629624-72-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(1R)-4-methylcyclohex-3-en-1-yl]pent-1-en-3-one

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:629624-72-2 SDS

629624-72-2Downstream Products

629624-72-2Relevant academic research and scientific papers

Convergent approaches to saudin intermediates

Cravero, Raquel M.,Gonzalez-Sierra, Manuel,Labadie, Guillermo R.

, p. 2741 - 2753 (2007/10/03)

Different convergent approaches to the highly oxygenated sesquiterpene natural product saudin (1), has been investigated. Our strategy has included a Michael addition and aldol condensation reaction as key steps. During the synthetic development, we have found serious steric hindrance when an α-Me-substituted alkyl vinyl ketone was used. Such steric hindrance has been overcome by synthesizing the vinyl ketone 16 through an anionic fragmentation, which was carefully studied. Finally, the intermediate 18 has been synthesized in a one-pot reaction from the vinyl ketone 16 and has been cyclized to obtain the promising tricyclic intermediate 20.

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