Cas 143238-02-2,(1R,1'S)-2'-[2,2-Dimethyl-prop-(E)-ylidene]-2-[2,2-dimethyl-prop-(Z)-ylidene]-bicyclohexyl

143238-02-2

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Basic information

Product Name: (1R,1'S)-2'-[2,2-Dimethyl-prop-(E)-ylidene]-2-[2,2-dimethyl-prop-(Z)-ylidene]-bicyclohexyl
Synonyms:
CAS NO:143238-02-2
Molecular Formula:
Molecular Weight: 302.544
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: (1R,1'S)-2'-[2,2-Dimethyl-prop-(E)-ylidene]-2-[2,2-dimethyl-prop-(Z)-ylidene]-bicyclohexyl(CAS DataBase Reference)
NIST Chemistry Reference: (1R,1'S)-2'-[2,2-Dimethyl-prop-(E)-ylidene]-2-[2,2-dimethyl-prop-(Z)-ylidene]-bicyclohexyl(143238-02-2)
EPA Substance Registry System: (1R,1'S)-2'-[2,2-Dimethyl-prop-(E)-ylidene]-2-[2,2-dimethyl-prop-(Z)-ylidene]-bicyclohexyl(143238-02-2)

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: 143238-02-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 143238-02-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,2,3 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 143238-02:
(8*1)+(7*4)+(6*3)+(5*2)+(4*3)+(3*8)+(2*0)+(1*2)=102
102 % 10 = 2
So 143238-02-2 is a valid CAS Registry Number.

143238-02-2Upstream product

69045-73-4 DL-3,4-Di(1-cyclohexen-1-yl)-2,2,5,5-tetramethylhexan

143238-02-2Downstream Products

143238-02-2Relevant academic research and scientific papers

Thermolabile Hydrocarbons, 32. - Competing Cope-Rearrangement and Homolytic Decomposition of meso- and DL-3,4-Di(1-cyclohexen-1-yl)-2,2,5,5-tetramethylhexane

Herberg, Clemens,Beckhaus, Hans-Dieter,Koertvelyesi, Tamas,Ruechardt, Christoph

, p. 117 - 128 (2007/10/02)

meso- and DL-3,4-Di(1-cyclohexen-1-yl)-2,2,5,5-tetramethylhexane (3a) were prepared by an improved reduction procedure (Li/C2H5NH2) from meso- and DL-2,2,5,5-tetramethyl-3,4-diphenylhexane.Products of two competing thermal transformations, C-C cleavage vs

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