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(E)-5-(cyclohex-3-en-1-ylidene)-2-methylhexan-3-yl formate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1392283-61-2

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1392283-61-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1392283-61-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,2,2,8 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1392283-61:
(9*1)+(8*3)+(7*9)+(6*2)+(5*2)+(4*8)+(3*3)+(2*6)+(1*1)=172
172 % 10 = 2
So 1392283-61-2 is a valid CAS Registry Number.

1392283-61-2Downstream Products

1392283-61-2Relevant academic research and scientific papers

NOVEL PROCESS

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Paragraph 0046; 0049-0050, (2014/09/30)

A direct acid catalyzed intermolecular electrocyclic rearrangement process for the preparation of linear and cyclic homoallylic ester and amides. A one step intermolecular electrocyclic rearrangement process includes the step of reacting a beta, gamma-unsaturated aldehyde or ketone, in which the beta, gamma-unsaturation is not part of an aromatic ring, with another aldehyde or a secondary aldimine in the presence of an acid.

NOVEL PROCESS

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Page/Page column 9; 10, (2013/05/21)

Disclosed is a direct acid catalyzed intermolecular electrocyclic rearrangement process for the preparation of linear and cyclic homoallylic ester and amides.

NOVEL PROCESS

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Page/Page column 9; 10, (2013/05/21)

Disclosed is a direct acid catalyzed intermolecular electrocyclic rearrangement process for the preparation of linear and cyclic homoallylic ester and amides.

Tandem cross-dimerisation/oxonia-cope reaction of carbonyl compounds to homoallylic esters and lactones

Zou, Yue,Ding, Changming,Zhou, Lijun,Li, Zhiming,Wang, Quanrui,Schoenebeck, Franziska,Goeke, Andreas

supporting information; experimental part, p. 5647 - 5651 (2012/07/13)

Conceptually different: This allyltransfer reaction is catalyzed by Lewis acids (LAs) and proceeds atom-economically by disproportionation of the carbonyl groups through organized oxonia-Cope transition states (see scheme). A stereoselective [n+4] ring enlargement leads to a variety of macrolides with 9- to 16-membered rings. Copyright

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