Cas 912365-40-3,(1S,12S)-N-benzyl-15,15-dimethyl-3-azatetracyclo[10.2.1.0(2,11).0(4,9)]pentadeca-2<sup>(11)</sup>,3,5,7,9-pentaen-1-ylmethanesulfonamide

912365-40-3

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Basic information

Product Name: (1S,12S)-N-benzyl-15,15-dimethyl-3-azatetracyclo[10.2.1.0(2,11).0(4,9)]pentadeca-2⁽¹¹⁾,3,5,7,9-pentaen-1-ylmethanesulfonamide
Synonyms: (1S,12S)-N-benzyl-15,15-dimethyl-3-azatetracyclo[10.2.1.0(2,11).0(4,9)]pentadeca-2⁽¹¹⁾,3,5,7,9-pentaen-1-ylmethanesulfonamide
CAS NO:912365-40-3
Molecular Formula:
Molecular Weight: 406.549
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: (1S,12S)-N-benzyl-15,15-dimethyl-3-azatetracyclo[10.2.1.0(2,11).0(4,9)]pentadeca-2⁽¹¹⁾,3,5,7,9-pentaen-1-ylmethanesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: (1S,12S)-N-benzyl-15,15-dimethyl-3-azatetracyclo[10.2.1.0(2,11).0(4,9)]pentadeca-2⁽¹¹⁾,3,5,7,9-pentaen-1-ylmethanesulfonamide(912365-40-3)
EPA Substance Registry System: (1S,12S)-N-benzyl-15,15-dimethyl-3-azatetracyclo[10.2.1.0(2,11).0(4,9)]pentadeca-2⁽¹¹⁾,3,5,7,9-pentaen-1-ylmethanesulfonamide(912365-40-3)

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: 912365-40-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 912365-40-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,2,3,6 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 912365-40:
(8*9)+(7*1)+(6*2)+(5*3)+(4*6)+(3*5)+(2*4)+(1*0)=153
153 % 10 = 3
So 912365-40-3 is a valid CAS Registry Number.

912365-40-3Upstream product

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912365-40-3Relevant academic research and scientific papers

Synthesis of camphorsulfonamide-based quinoline ligands and their N-oxides: first use in the enantioselective addition of organozinc reagents to aldehydes

Martinez, Ricardo,Zoli, Luca,Cozzi, Pier Giorgio,Ramon, Diego J.,Yus, Miguel

, p. 2600 - 2607 (2008)

The preparation of several camphorsulfonamide-based quinoline derivatives and their N-oxides was accomplished via an indirect Friedlaender synthesis using aminobenzylic alcohols and RuCl2(DMSO)4 as a catalyst. These ligands were tested in the enantioselective addition of dialkylzinc reagents to aldehydes, with enantiomeric excesses up to 96%. A similar protocol using triphenylborane and diethylzinc gave the corresponding phenylation process.

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