Cas 812649-82-4,1-[(3S,4R,5S,6S)-4-(tert-Butyl-dimethyl-silanyloxy)-2-hydroxy-6-isopropenyl-3,5-dimethyl-cyclohex-1-enyl]-ethanone

812649-82-4

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Basic information

Product Name: 1-[(3S,4R,5S,6S)-4-(tert-Butyl-dimethyl-silanyloxy)-2-hydroxy-6-isopropenyl-3,5-dimethyl-cyclohex-1-enyl]-ethanone
Synonyms: 1-[(3S,4R,5S,6S)-4-(tert-Butyl-dimethyl-silanyloxy)-2-hydroxy-6-isopropenyl-3,5-dimethyl-cyclohex-1-enyl]-ethanone
CAS NO:812649-82-4
Molecular Formula:
Molecular Weight: 338.563
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: 1-[(3S,4R,5S,6S)-4-(tert-Butyl-dimethyl-silanyloxy)-2-hydroxy-6-isopropenyl-3,5-dimethyl-cyclohex-1-enyl]-ethanone(CAS DataBase Reference)
NIST Chemistry Reference: 1-[(3S,4R,5S,6S)-4-(tert-Butyl-dimethyl-silanyloxy)-2-hydroxy-6-isopropenyl-3,5-dimethyl-cyclohex-1-enyl]-ethanone(812649-82-4)
EPA Substance Registry System: 1-[(3S,4R,5S,6S)-4-(tert-Butyl-dimethyl-silanyloxy)-2-hydroxy-6-isopropenyl-3,5-dimethyl-cyclohex-1-enyl]-ethanone(812649-82-4)

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: 812649-82-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 812649-82-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,2,6,4 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 812649-82:
(8*8)+(7*1)+(6*2)+(5*6)+(4*4)+(3*9)+(2*8)+(1*2)=174
174 % 10 = 4
So 812649-82-4 is a valid CAS Registry Number.

812649-82-4Upstream product

812649-82-4Downstream Products

812649-82-4Relevant academic research and scientific papers

Formation of highly substituted chiral cyclohexanone derivatives using a tandem conjugate addition/cyclisation

Jeffery, David W.,Perkins, Michael V.

, p. 8667 - 8671 (2007/10/03)

A tandem conjugate addition/cyclisation approach, that allows the synthesis of chiral highly substituted cyclohexanones and cyclohexenones, which is applicable to natural product syntheses has been developed. A tandem conjugate addition/cyclisation approa

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