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2,6-diallyl-1-cyclohexanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

36040-02-5

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36040-02-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36040-02-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,0,4 and 0 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 36040-02:
(7*3)+(6*6)+(5*0)+(4*4)+(3*0)+(2*0)+(1*2)=75
75 % 10 = 5
So 36040-02-5 is a valid CAS Registry Number.

36040-02-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-diallyl-1-cyclohexanone

1.2 Other means of identification

Product number -
Other names 2,6-Diallyl-cyclohexanon

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:36040-02-5 SDS

36040-02-5Relevant academic research and scientific papers

Organic Compounds

-

Page/Page column 26, (2010/12/18)

Described are spiroalkyl- and -alkenylketones and esters thereof, a method for their production and fragrance compositions comprising them.

Synthesis of the Tricyclo3,8>pentadecane (ABC) Ring System of Taxane Diterpenes

Romero, Miguel A.,Franco, Ruben Perez,Cruz-Almanza, Raymundo,Padilla, Fernando

, p. 3255 - 3258 (2007/10/02)

The synthesis of diketone 14 possessing the tricyclo3,8>pentadecane (ABC) taxane ring system is described.This concise approach employs a Wacker oxidation, intramolecular aldol condensation-dehydration, and a highly exo-stereoselective

2-Allylisourea as an Effective Agent for Direct α-Allylation of Ketone and Aldehyde Assisted by Palladium(0) under Neutral Conditions

Inoue, Yoshio,Toyofuku, Masanori,Taguchi, Masaaki,Okada, Shin-ichi,Hashimoto, Harukichi

, p. 885 - 892 (2007/10/02)

Direct α-allylation of a variety of ketones and aldehydes with 2-allylisourea took place in the presence of a catalytic amount of a palladium(0) complex under neutral and mild conditions.Scope and limitations of this novel method have been investigated.

Palladium-catalysed Asymmetric Allylations by a Chiral Allyl Ester; the Palladium Catalysis of (S)-Proline Allyl Ester Enamines

Hiroi, Kunio,Suya, Kyoko,Sato, Shuko

, p. 469 - 470 (2007/10/02)

The palladium-catalysed allylation of the chiral enamines (1a-d) followed by acidic hydrolysis, produced optically active 2-allylcyclohexanone (2); the catalysis of the chiral enamine (1a), derived from (S)-proline allyl ester, with tetrakis(triphenyl pho

NUCLEOPHILIC SUBSTITUTION REACTIONS OF ALLYLIC ESTERS CATALYSED BY PALLADIUM-GRAPHITE AND RELATED HETEROGENEOUS CATALYSTS

Boldrini, Gian Paolo,Savoia, Diego,Tagliavini, Emilio,Trombini, Claudio,Umani-Ronchi, Achille

, p. 97 - 106 (2007/10/02)

Highly dispersed palladium on graphite (Pd/Gr), carbon (Pd/C) and alumina (Pd/Al2O3) have been employed as catalysts in substitution reactions of allylic esters with nucleophiles such as benzenesulfinate and diethyl malonate anions, and 1-(1-cyclohexen-1-yl)pyrrolidine.

DIRECT Α-ALLYLATION OF KETONES WITH O-ALLYLISOUREA CATALYZED BY PALLADIUM(0)

Inoue, Yoshio,Toyofuku, Masanori,Hashimoto, Harukichi

, p. 1227 - 1228 (2007/10/02)

Direct α-allylation of ketones catalyzed by a palladium(0)-diphosphine system took place employing O-allylisourea as the allylating reagent under neutral conditions ar room temperature in DMF.

SYNTHESIS OF γ,δ-UNSATURATED KETONES BY THE INTRAMOLECULAR DECARBOXYLATIVE ALLYLATION OF ALLYL β-KETO CARBOXYLATES AND ALKENYL ALLYL CARBONATES CATALYZED BY MOLYBDENUM, NICKEL, AND RHODIUM COMPLEXES

Tsuji, Jiro,Minami, Ichiro,Shimizu, Isao

, p. 1721 - 1724 (2007/10/02)

Allyl β-keto carboxylates and alkenyl allyl carbonates were converted to γ,δ-unsaturated ketones by the intramolecular decarboxylative allylation catalyzed by molybdenum, nickel, and rhodium complexes.

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