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5-(tert-butyl)-2-chlorocyclohex-1-enecarbaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81292-71-9

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81292-71-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81292-71-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,2,9 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 81292-71:
(7*8)+(6*1)+(5*2)+(4*9)+(3*2)+(2*7)+(1*1)=129
129 % 10 = 9
So 81292-71-9 is a valid CAS Registry Number.

81292-71-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(tertbutyl)-2-chlorocyclohex-1-enecarbaldehyde

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:81292-71-9 SDS

81292-71-9Relevant academic research and scientific papers

Efficient synthesis of 4- And 5-substituted 2-aminopyrimidines by coupling of β-Chlorovinyl Aldehydes and Guanidines

Komendantova, Anna S.,Komkov, Alexander V.,Volkova, Yulia A.,Zavarzin, Igor V.

supporting information, p. 4247 - 4254 (2018/08/24)

A general, practical, and simple synthesis of functionalized 2-aminopyrimidines starting from β-chlorovinyl aldehydes and amidines is reported. In the presence of potassium carbonate, various ketones have been efficiently transformed into the pyrimidine derivatives by a two-step sequence involving the Vilsmeier-Haack reaction followed by a condensation reaction with guanidines. The protocol is distinguished by operational simplicity, inexpensive reagents, and functional-group tolerance. In many cases, pure solid products can be obtained in high to excellent yields without using column chromatography. The synthetic value of the method was demonstrated by the efficient synthesis of steroidal pyrimidines and a precursor of the antitumor agents Imatinib and Mocetinostat.

A Straightforward Approach toward Multifunctionalized Pyridazines via Imination/Electrocyclization

Komkov, Alexander V.,Komendantova, Anna S.,Menchikov, Leonid G.,Chernoburova, Elena I.,Volkova, Yulia A.,Zavarzin, Igor V.

supporting information, p. 3734 - 3737 (2015/08/18)

A facile synthesis of functionalized 3-carbamide pyridazines starting from readily available chlorovinyl aldehydes and oxamic acid thiohydrazides via cascade imination/electrocyclization is reported. In the presence of p-toluenesulfuric acid, various ketones have been efficiently incorporated into the pyridazine derivatives through a two-step sequence involving a Vilsmeier-Haack reaction and imination. The synthetic value of this method has been demonstrated by efficient synthesis of steroidal pyridazines.

Intramolecular Fe(II)-Catalyzed N-O or N-N bond formation from aryl azides

Stokes, Benjamin J.,Vogel, Carl V.,Urnezis, Linda K.,Pan, Minjie,Driver, Tom G.

supporting information; experimental part, p. 2884 - 2887 (2010/08/21)

(Figure presented) Iron(II) bromide catalyzes the transformation of aryl and vinyl azides with ketone or methyl oxime substituents into 2,1-benzisoxazoles, indazoles, or pyrazoles through the formation of an N-O or N-N bond. This transformation tolerates a variety of different functional groups to facilitate access to a range of benzisoxazoles or indazoles. The unreactivity of the Z-methyloxime indicates that N-heterocycle formation occurs through a nucleophilic attack of the ketone or oxime onto an activated planar iron azide complex.

Relevance of oxyanion stereochemistry to chirality transfer in anionic oxy-cope rearrangements

Paquette, Leo A.,Maynard, George D.

, p. 5018 - 5027 (2007/10/02)

Geometrically and optically pure (3R,5E)- and (3R,5Z)-1,5-heptadien-3-ols undergo anionic oxy-Cope rearrangement under the exclusive control of oxyanion orientation with a 58-64% preference for equatorial oxygen. Six semicyclic dienols have also been synthesized where the preferred oxyanion-driven sigmatropic rearrangement pathway is obligatorily pitted against π-facial biases offered by 4-tert-butylcyclohexenyl, norbornenyl, and camphersyl rings. These rearrangements therefore offer especially stringent tests of those factors that control the level and direction of chirality transfer. The data show the oxyanion to disfavor becoming involved in 1,3-diaxial relationships. Electronic factors may also contribute to the stabilization of axial oxyanion orientation. If operative, this effect cannot be large and is easily overridden. The observed preferences show that a change in relative carbinol configuration can indeed have a significant impact on the isomeric distribution obtained from the anionic oxy-Cope rearrangement.

Synthesis of 5-tert-Butylbenzothiophene-2-carboxylic Acid

Gallagher, Peter T.,Owton, W. Martin

, p. 2731 - 2736 (2007/10/02)

The title compound was prepared from 4-tert-butyl cyclohexanone in high yield by a simple three step procedure.

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