Cas 1058705-68-2,[6S,7S,9(1S)]-9-[1-(dibenzylamino)-2-phenylethyl]-7-methylbicyclo[4.3.0]non-1<sup>(9)</sup>-en-8-one

1058705-68-2

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Basic information

Product Name: [6S,7S,9(1S)]-9-[1-(dibenzylamino)-2-phenylethyl]-7-methylbicyclo[4.3.0]non-1⁽⁹⁾-en-8-one
Synonyms: [6S,7S,9(1S)]-9-[1-(dibenzylamino)-2-phenylethyl]-7-methylbicyclo[4.3.0]non-1⁽⁹⁾-en-8-one
CAS NO:1058705-68-2
Molecular Formula:
Molecular Weight: 449.636
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: [6S,7S,9(1S)]-9-[1-(dibenzylamino)-2-phenylethyl]-7-methylbicyclo[4.3.0]non-1⁽⁹⁾-en-8-one(CAS DataBase Reference)
NIST Chemistry Reference: [6S,7S,9(1S)]-9-[1-(dibenzylamino)-2-phenylethyl]-7-methylbicyclo[4.3.0]non-1⁽⁹⁾-en-8-one(1058705-68-2)
EPA Substance Registry System: [6S,7S,9(1S)]-9-[1-(dibenzylamino)-2-phenylethyl]-7-methylbicyclo[4.3.0]non-1⁽⁹⁾-en-8-one(1058705-68-2)

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: 1058705-68-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1058705-68-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,8,7,0 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1058705-68:
(9*1)+(8*0)+(7*5)+(6*8)+(5*7)+(4*0)+(3*5)+(2*6)+(1*8)=162
162 % 10 = 2
So 1058705-68-2 is a valid CAS Registry Number.

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1058705-68-2Relevant academic research and scientific papers

Asymmetric synthesis of 3,4-annulated cyclopentenones from cycloalkenyl ketones and vinyl carbamates by diastereoselective carbonyl addition/conrotatory 4π ring closure

Siemer, Michael,Froehlich, Roland,Hoppe, Dieter

experimental part, p. 2264 - 2270 (2009/04/07)

1-Lithiated O-vinyl carbamates add with high induced diastereoselectivity onto enantiomerically pure cycloalk-1-enyl (1-dibenzylamino)alkyl ketones. Subsequent O-carbamoyl migration, followed by a torquoselective, antarafacial 4π ring closure, leads to ho

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