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Cyclohexanecarboxylic acid, 1-[(acetyloxy)methyl]-2-oxo-, 2-propenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106729-33-3

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106729-33-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106729-33-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,7,2 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 106729-33:
(8*1)+(7*0)+(6*6)+(5*7)+(4*2)+(3*9)+(2*3)+(1*3)=123
123 % 10 = 3
So 106729-33-3 is a valid CAS Registry Number.

106729-33-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name allyl 1-(acetoxymethyl)-2-oxocyclohexanecarboxylate

1.2 Other means of identification

Product number -
Other names 1-Acetoxymethyl-2-oxo-cyclohexanecarboxylic acid allyl ester

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:106729-33-3 SDS

106729-33-3Downstream Products

106729-33-3Relevant academic research and scientific papers

PREPARATION OF α-METHYLENE KETONES BY THE PALLADIUM-CATALYZED DECARBOXYLATION-DEACETOXYLATION OF ALLYL α-ACETOXYMETHYL-β-KETO CARBOXYLATES UNDER MILD CONDITIONS

Tsuji, Jiro,Nisar, Mohammad,Minami, Ichiro

, p. 2483 - 2486 (1986)

α-Methylene ketones are prepared in high yields by the palladium-catalyzed decarboxylation-deacetoxylation of allyl α-acetoxymethyl-β-keto carboxylates.The reaction proceeds rapidly at room temperature under neutral conditions in acetonitrile.

Synthesis and olfactory properties of spirocyclic Georgywood analogues

Kraft, Philip,Frech, David,Mueller, Urs,Frater, Georg

, p. 2215 - 2223 (2006)

Spirocyclic analogues of Georgywood (3) and unlike-10-acetyl-9,10- dimethylbicyclo[6.4.0]dodec-1(8)-ene (4), in which the acetyl moiety and the methyl substituent of C-10 are part of a cyclopentyl or cyclohexyl ring, were synthesized from 8a-homomyrcene (

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