Cas 374111-80-5,(1S,2R,3R,5R)-2-(tert-Butyl-dimethyl-silanyloxy)-4-[(R)-2-hydroxy-2-phenyl-eth-(Z)-ylidene]-6,6-dimethyl-bicyclo[3.1.1]heptan-3-ol

374111-80-5

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Basic information

Product Name: (1S,2R,3R,5R)-2-(tert-Butyl-dimethyl-silanyloxy)-4-[(R)-2-hydroxy-2-phenyl-eth-(Z)-ylidene]-6,6-dimethyl-bicyclo[3.1.1]heptan-3-ol
Synonyms:
CAS NO:374111-80-5
Molecular Formula:
Molecular Weight: 388.623
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: (1S,2R,3R,5R)-2-(tert-Butyl-dimethyl-silanyloxy)-4-[(R)-2-hydroxy-2-phenyl-eth-(Z)-ylidene]-6,6-dimethyl-bicyclo[3.1.1]heptan-3-ol(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2R,3R,5R)-2-(tert-Butyl-dimethyl-silanyloxy)-4-[(R)-2-hydroxy-2-phenyl-eth-(Z)-ylidene]-6,6-dimethyl-bicyclo[3.1.1]heptan-3-ol(374111-80-5)
EPA Substance Registry System: (1S,2R,3R,5R)-2-(tert-Butyl-dimethyl-silanyloxy)-4-[(R)-2-hydroxy-2-phenyl-eth-(Z)-ylidene]-6,6-dimethyl-bicyclo[3.1.1]heptan-3-ol(374111-80-5)

Safety Data

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Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 374111-80-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 374111-80-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,4,1,1 and 1 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 374111-80:
(8*3)+(7*7)+(6*4)+(5*1)+(4*1)+(3*1)+(2*8)+(1*0)=125
125 % 10 = 5
So 374111-80-5 is a valid CAS Registry Number.

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374111-80-5Relevant academic research and scientific papers

A novel reactivity of SeO(2) with 1,3-dienes: formation of syn 1,2- and 1,4-diols via a facile C-Se bond oxidation.

Nguyen,Lee

, p. 3161 - 3163 (2007/10/03)

[reaction: see text] A novel reaction between 1,3-dienes and selenium dioxide to give syn 1,2- and 1,4-diol cyclic selenites was studied in detail. This study indicates that an initial concerted [4 + 2] cycloaddition followed by a stereospecific carbon-se

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