Cas 6582-68-9,(2R,3R,5R,11S,22S)-3,11-Methanoaspidofractinin-22-ol

6582-68-9

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Basic information

Product Name: (2R,3R,5R,11S,22S)-3,11-Methanoaspidofractinin-22-ol
Synonyms: (22S)-Kopsan-22-ol;(2R,3R,5R,11S,22S)-3,11-Methanoaspidofractinin-22-ol;Kopsanol
CAS NO:6582-68-9
Molecular Formula: C20H24N2O
Molecular Weight: 308.41736
EINECS: N/A
Product Categories: N/A
Mol File: 6582-68-9.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (2R,3R,5R,11S,22S)-3,11-Methanoaspidofractinin-22-ol(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R,5R,11S,22S)-3,11-Methanoaspidofractinin-22-ol(6582-68-9)
EPA Substance Registry System: (2R,3R,5R,11S,22S)-3,11-Methanoaspidofractinin-22-ol(6582-68-9)

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: 6582-68-9(Hazardous Substances Data)

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References

Filho et al., J. Chem. Soc., C, 1260 (1966)

Check Digit Verification of cas no

The CAS Registry Mumber 6582-68-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,8 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6582-68:
(6*6)+(5*5)+(4*8)+(3*2)+(2*6)+(1*8)=119
119 % 10 = 9
So 6582-68-9 is a valid CAS Registry Number.

6582-68-9Upstream product

6582-68-9Downstream Products

6582-68-9Relevant academic research and scientific papers

Synthesis of (+/-)-10,22-Dioxokopsane and (+/-)-Kopsanone, Heptacyclic Indole Alkaloids. Synthetic and Mechanistic Studies

Magnus, Philip,Gallagher, Timothy,Brown, Peter,Huffman, John C.

, p. 2105 - 2114 (2007/10/02)

The total synthesis of the heptacyclic indole alkaloids (+/-)-10,22-dioxokopsane (2) and (+/-)-kopsanone (3, X=O) is described.The imine 20 was condensed with β,β,β-trichloroethyl chloroformate to give the tetracyclic carbamate 21.Removal of the carbamate

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