Cas 824391-48-2,Pentaleno[1,6-bc]oxocin-6(2H)-one, 3,4,5,7,7a,8,9,9a-octahydro-, (7aR,9aR)-rel- (9CI)

824391-48-2

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Basic information

Product Name: Pentaleno[1,6-bc]oxocin-6(2H)-one, 3,4,5,7,7a,8,9,9a-octahydro-, (7aR,9aR)-rel- (9CI)
Synonyms: Pentaleno[1,6-bc]oxocin-6(2H)-one, 3,4,5,7,7a,8,9,9a-octahydro-, (7aR,9aR)-rel- (9CI)
CAS NO:824391-48-2
Molecular Formula: C12H16O2
Molecular Weight: 192.25
EINECS: N/A
Product Categories: CYCLOPENTANE

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: Pentaleno[1,6-bc]oxocin-6(2H)-one, 3,4,5,7,7a,8,9,9a-octahydro-, (7aR,9aR)-rel- (9CI)(CAS DataBase Reference)
NIST Chemistry Reference: Pentaleno[1,6-bc]oxocin-6(2H)-one, 3,4,5,7,7a,8,9,9a-octahydro-, (7aR,9aR)-rel- (9CI)(824391-48-2)
EPA Substance Registry System: Pentaleno[1,6-bc]oxocin-6(2H)-one, 3,4,5,7,7a,8,9,9a-octahydro-, (7aR,9aR)-rel- (9CI)(824391-48-2)

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: 824391-48-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 824391-48-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,4,3,9 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 824391-48:
(8*8)+(7*2)+(6*4)+(5*3)+(4*9)+(3*1)+(2*4)+(1*8)=172
172 % 10 = 2
So 824391-48-2 is a valid CAS Registry Number.

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824391-48-2Relevant academic research and scientific papers

Tandem intramolecular Nicholas and Pauson - Khand reactions for the synthesis of tricyclic oxygen-containing heterocycles

Quintal, Miriam M.,Closser, Kristina D.,Shea, Kevin M.

, p. 4949 - 4952 (2004)

(Chemical Equation Presented) Simple acyclic enynes can be easily converted into tricyclic ethers upon treatment with Co2(CO)8 followed by Nicholas and Pauson - Khand reactions. Tricyclic [5,8,5]- and [5,7,5]-systems can be prepared in high overall yields in only seven synthetic steps.

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