Cas 129194-20-3,(E)-4-<2-methyl-4-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2-butenyl>-3-cyclohexen-1-one

129194-20-3

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Basic information

Product Name: (E)-4-<2-methyl-4-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2-butenyl>-3-cyclohexen-1-one
Synonyms: (E)-4-<2-methyl-4-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2-butenyl>-3-cyclohexen-1-one
CAS NO:129194-20-3
Molecular Formula:
Molecular Weight: 286.458
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: (E)-4-<2-methyl-4-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2-butenyl>-3-cyclohexen-1-one(CAS DataBase Reference)
NIST Chemistry Reference: (E)-4-<2-methyl-4-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2-butenyl>-3-cyclohexen-1-one(129194-20-3)
EPA Substance Registry System: (E)-4-<2-methyl-4-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2-butenyl>-3-cyclohexen-1-one(129194-20-3)

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: 129194-20-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 129194-20-3 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, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 129194-20:
(8*1)+(7*2)+(6*9)+(5*1)+(4*9)+(3*4)+(2*2)+(1*0)=133
133 % 10 = 3
So 129194-20-3 is a valid CAS Registry Number.

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129194-20-3Relevant 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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