Cas 1245809-68-0,N-((1R,2R)-2-(4-(3,5-dimethylcyclohexa-1,4-dienyl)-butylamino)-1,2-diphenylethyl)-4-methylbenzene-sulfonamide

1245809-68-0

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Basic information

Product Name: N-((1R,2R)-2-(4-(3,5-dimethylcyclohexa-1,4-dienyl)-butylamino)-1,2-diphenylethyl)-4-methylbenzene-sulfonamide
Synonyms:
CAS NO:1245809-68-0
Molecular Formula:
Molecular Weight: 528.759
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-((1R,2R)-2-(4-(3,5-dimethylcyclohexa-1,4-dienyl)-butylamino)-1,2-diphenylethyl)-4-methylbenzene-sulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-((1R,2R)-2-(4-(3,5-dimethylcyclohexa-1,4-dienyl)-butylamino)-1,2-diphenylethyl)-4-methylbenzene-sulfonamide(1245809-68-0)
EPA Substance Registry System: N-((1R,2R)-2-(4-(3,5-dimethylcyclohexa-1,4-dienyl)-butylamino)-1,2-diphenylethyl)-4-methylbenzene-sulfonamide(1245809-68-0)

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: 1245809-68-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1245809-68-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,5,8,0 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1245809-68:
(9*1)+(8*2)+(7*4)+(6*5)+(5*8)+(4*0)+(3*9)+(2*6)+(1*8)=170
170 % 10 = 0
So 1245809-68-0 is a valid CAS Registry Number.

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1245809-68-0Relevant academic research and scientific papers

Asymmetric transfer hydrogenation of quinolines using tethered Ru(II) catalysts

Parekh, Vimal,Ramsden, James A.,Wills, Martin

experimental part, p. 1549 - 1556 (2010/11/02)

The first report of an asymmetric transfer hydrogenation, in formic acid/triethylamine, of quinolines is described. Using a Ru(II) catalyst containing a 4-carbon tether, products of up to 73% ee were formed, whilst a Rh(III)-tethered catalyst gave products of up to 94% ee.

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