Cas 295320-60-4,(2S,10bR)-2-benzyl-1-(p-tolylsulfonyl)-1,10b-dihydroimidazo[2,1-a]isoquinolin-3(2H)-one

295320-60-4

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Basic information

Product Name: (2S,10bR)-2-benzyl-1-(p-tolylsulfonyl)-1,10b-dihydroimidazo[2,1-a]isoquinolin-3(2H)-one
Synonyms: (2S,10bR)-2-benzyl-1-(p-tolylsulfonyl)-1,10b-dihydroimidazo[2,1-a]isoquinolin-3(2H)-one
CAS NO:295320-60-4
Molecular Formula:
Molecular Weight: 430.527
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: (2S,10bR)-2-benzyl-1-(p-tolylsulfonyl)-1,10b-dihydroimidazo[2,1-a]isoquinolin-3(2H)-one(CAS DataBase Reference)
NIST Chemistry Reference: (2S,10bR)-2-benzyl-1-(p-tolylsulfonyl)-1,10b-dihydroimidazo[2,1-a]isoquinolin-3(2H)-one(295320-60-4)
EPA Substance Registry System: (2S,10bR)-2-benzyl-1-(p-tolylsulfonyl)-1,10b-dihydroimidazo[2,1-a]isoquinolin-3(2H)-one(295320-60-4)

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: 295320-60-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 295320-60-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,5,3,2 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 295320-60:
(8*2)+(7*9)+(6*5)+(5*3)+(4*2)+(3*0)+(2*6)+(1*0)=144
144 % 10 = 4
So 295320-60-4 is a valid CAS Registry Number.

295320-60-4Upstream product

119-65-3 isoquinoline

295320-60-4Downstream Products

295320-60-4Relevant academic research and scientific papers

Asymmetric synthesis of isoquinoline derivatives from amino acids

Sieck, Oxana,Ehwald, Max,Liebscher, Juergen

, p. 663 - 672 (2005)

Reaction of isoquinolines 1 with N-arylsulfonylamino acid fluorides 2 provides a highly stereoselective access to new dihydroimidazo[2,1-a] isoquinolin-3-ones 5 via intermediate N-acylisoquinolinium salts 3. Addition reactions to the enamine double bond,

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