Cas 129194-19-0,(S)-4-<<4-(1-methylethenyl)-1-cyclohexen-1-yl>methyl>-3-cyclohexen-1-one

129194-19-0

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Basic information

Product Name: (S)-4-<<4-(1-methylethenyl)-1-cyclohexen-1-yl>methyl>-3-cyclohexen-1-one
Synonyms: (S)-4-<<4-(1-methylethenyl)-1-cyclohexen-1-yl>methyl>-3-cyclohexen-1-one
CAS NO:129194-19-0
Molecular Formula:
Molecular Weight: 230.35
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (S)-4-<<4-(1-methylethenyl)-1-cyclohexen-1-yl>methyl>-3-cyclohexen-1-one(CAS DataBase Reference)
NIST Chemistry Reference: (S)-4-<<4-(1-methylethenyl)-1-cyclohexen-1-yl>methyl>-3-cyclohexen-1-one(129194-19-0)
EPA Substance Registry System: (S)-4-<<4-(1-methylethenyl)-1-cyclohexen-1-yl>methyl>-3-cyclohexen-1-one(129194-19-0)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 129194-19-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 129194-19-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,1,9 and 4 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 129194-19:
(8*1)+(7*2)+(6*9)+(5*1)+(4*9)+(3*4)+(2*1)+(1*9)=140
140 % 10 = 0
So 129194-19-0 is a valid CAS Registry Number.

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129194-19-0Relevant academic research and scientific papers

4-alkenyl-1-methoxy-1,4-cyclohexadienes by tandem addition-multistep reduction of alkenyl aldehydes and ketones. Synthesis of 4-alkenyl-3-cyclohexen-1-ones by subsequent hydrolysis

Flisak, Joseph R.,Hall, Stan S.

, p. 7299 - 7305 (2007/10/02)

A series of 4-alkenyl-1-methoxy-1,4-cyclohexadienes were prepared by a tandem addition-multistep reduction procedure. This one-pot process included the addition of 4-methoxyphenyllithium to alkenyl aldehydes and ketones, followed by multistep reduction of

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