Cas 444192-82-9,N-{(3aS,6aS)-2-[(1R)-1-phenylethyl]octahydrocyclopenta[c]pyrrol-3a-ylcarbonyl}-(2R)-bornane-10,2-sultam

444192-82-9

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Basic information

Product Name: N-{(3aS,6aS)-2-[(1R)-1-phenylethyl]octahydrocyclopenta[c]pyrrol-3a-ylcarbonyl}-(2R)-bornane-10,2-sultam
Synonyms: N-{(3aS,6aS)-2-[(1R)-1-phenylethyl]octahydrocyclopenta[c]pyrrol-3a-ylcarbonyl}-(2R)-bornane-10,2-sultam
CAS NO:444192-82-9
Molecular Formula:
Molecular Weight: 456.649
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: N-{(3aS,6aS)-2-[(1R)-1-phenylethyl]octahydrocyclopenta[c]pyrrol-3a-ylcarbonyl}-(2R)-bornane-10,2-sultam(CAS DataBase Reference)
NIST Chemistry Reference: N-{(3aS,6aS)-2-[(1R)-1-phenylethyl]octahydrocyclopenta[c]pyrrol-3a-ylcarbonyl}-(2R)-bornane-10,2-sultam(444192-82-9)
EPA Substance Registry System: N-{(3aS,6aS)-2-[(1R)-1-phenylethyl]octahydrocyclopenta[c]pyrrol-3a-ylcarbonyl}-(2R)-bornane-10,2-sultam(444192-82-9)

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: 444192-82-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 444192-82-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,4,1,9 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 444192-82:
(8*4)+(7*4)+(6*4)+(5*1)+(4*9)+(3*2)+(2*8)+(1*2)=149
149 % 10 = 9
So 444192-82-9 is a valid CAS Registry Number.

444192-82-9Upstream product

444192-82-9Downstream Products

2696257-98-2 (3aS,6aS)-octahydrocyclopenta[c]pyrrol-3a-ylmethanol

444192-82-9Relevant academic research and scientific papers

Diastereoselective addition of chiral azomethine ylides to cyclic α,β-unsaturated N-enoylbornanesultams

Karlsson, Staffan,Hoegberg, Hans-Erik

, p. 1076 - 1082 (2007/10/03)

Doubly diastereoselective 1,3-dipolar cycloaddition reactions of chiral non-racemic azomethine ylides to cyclic five-and six-membered α,β-unsaturated N-enoylbornanesultams were carried out. When suitable solvents were used, the fused bicyclic adducts form

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