Cas 1063674-45-2,(1R,5S,8S,12R)-5-((tert-butyldiphenylsilyloxy)methyl)-12-cyano-6-aza-7-oxatricyclo[6.3.1.0(1,6)]dodecane

1063674-45-2

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Basic information

Product Name: (1R,5S,8S,12R)-5-((tert-butyldiphenylsilyloxy)methyl)-12-cyano-6-aza-7-oxatricyclo[6.3.1.0(1,6)]dodecane
Synonyms: (1R,5S,8S,12R)-5-((tert-butyldiphenylsilyloxy)methyl)-12-cyano-6-aza-7-oxatricyclo[6.3.1.0(1,6)]dodecane
CAS NO:1063674-45-2
Molecular Formula:
Molecular Weight: 460.692
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,5S,8S,12R)-5-((tert-butyldiphenylsilyloxy)methyl)-12-cyano-6-aza-7-oxatricyclo[6.3.1.0(1,6)]dodecane(CAS DataBase Reference)
NIST Chemistry Reference: (1R,5S,8S,12R)-5-((tert-butyldiphenylsilyloxy)methyl)-12-cyano-6-aza-7-oxatricyclo[6.3.1.0(1,6)]dodecane(1063674-45-2)
EPA Substance Registry System: (1R,5S,8S,12R)-5-((tert-butyldiphenylsilyloxy)methyl)-12-cyano-6-aza-7-oxatricyclo[6.3.1.0(1,6)]dodecane(1063674-45-2)

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: 1063674-45-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1063674-45-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,3,6,7 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1063674-45:
(9*1)+(8*0)+(7*6)+(6*3)+(5*6)+(4*7)+(3*4)+(2*4)+(1*5)=152
152 % 10 = 2
So 1063674-45-2 is a valid CAS Registry Number.

1063674-45-2Upstream product

1063674-42-9 (2S,6S,8R)-2-((tert-butyldiphenylsilyloxy)methyl)-6-(5'-cyanopent-4'-en-1'-yl)-8-phenyl-1-aza-9-oxabicyclo[4.3.0]nonane

1063674-45-2Downstream Products

1063674-66-7 C₂₈H₃₇NO₃Si

1063674-45-2Relevant academic research and scientific papers

Total synthesis of (-)-histrionicotoxin 285A and (-)- perhydrohistrionicotoxin

Macdonald, James M.,Horsley, Helen T.,Ryan, John H.,Saubern, Simon,Holmes, Andrew B.

supporting information; experimental part, p. 4227 - 4229 (2009/06/06)

(Chemical Equation Presented) Starting from commercially available (S)-glycidol, and via a common intermediate, the total synthesis of (-)-histrionicotoxin 285A and (-)-perhydrohistrionicotoxin has been achieved. Key to this synthesis was the efficient co

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