Cas 122211-75-0,(1R,3S)-5-[2-[(1R,7aR)-1-((R)-1,5-Dimethyl-hex-5-enyl)-7a-methyl-1,2,7,7a-tetrahydro-inden-(4Z)-ylidene]-eth-(Z)-ylidene]-4-methyl-cyclohexane-1,3-diol

122211-75-0

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Basic information

Product Name: (1R,3S)-5-[2-[(1R,7aR)-1-((R)-1,5-Dimethyl-hex-5-enyl)-7a-methyl-1,2,7,7a-tetrahydro-inden-(4Z)-ylidene]-eth-(Z)-ylidene]-4-methyl-cyclohexane-1,3-diol
Synonyms:
CAS NO:122211-75-0
Molecular Formula:
Molecular Weight: 396.613
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,3S)-5-[2-[(1R,7aR)-1-((R)-1,5-Dimethyl-hex-5-enyl)-7a-methyl-1,2,7,7a-tetrahydro-inden-(4Z)-ylidene]-eth-(Z)-ylidene]-4-methyl-cyclohexane-1,3-diol(CAS DataBase Reference)
NIST Chemistry Reference: (1R,3S)-5-[2-[(1R,7aR)-1-((R)-1,5-Dimethyl-hex-5-enyl)-7a-methyl-1,2,7,7a-tetrahydro-inden-(4Z)-ylidene]-eth-(Z)-ylidene]-4-methyl-cyclohexane-1,3-diol(122211-75-0)
EPA Substance Registry System: (1R,3S)-5-[2-[(1R,7aR)-1-((R)-1,5-Dimethyl-hex-5-enyl)-7a-methyl-1,2,7,7a-tetrahydro-inden-(4Z)-ylidene]-eth-(Z)-ylidene]-4-methyl-cyclohexane-1,3-diol(122211-75-0)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
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Hazardous Substances Data: 122211-75-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 122211-75-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,2,1 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 122211-75:
(8*1)+(7*2)+(6*2)+(5*2)+(4*1)+(3*1)+(2*7)+(1*5)=70
70 % 10 = 0
So 122211-75-0 is a valid CAS Registry Number.

122211-75-0Upstream product

122172-41-2 (1S,3S,6R)-9,10-secocholesta-5⁽¹⁰⁾,6,7,9⁽¹¹⁾,25-pentaene-1,3-diol

122211-75-0Downstream Products

122211-75-0Relevant academic research and scientific papers

Synthesis and Biological Activity of 9,11-Dehydrovitamin D3 analogues: Stereoselctive Preparation of 6β-Vitamin D Vinylallenes and a Concise Enynol Synthesis for Preparing the A-Ring

Okamura, William H.,Aurrecoechea, J. Miguel,Gibbs, Richard A.,Norman, Anthony W.

, p. 4072 - 4083 (1989)

The Δ9(11)-unsaturated vitamin D analogues 5a and 5b are of biochemical interest because they are incapable of tautomerizing via a sigmatropic hydrogen shift to a previtamin structure related to 3 and also becouse they possess a perturbed

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