Cas 1609623-89-3,(3S,4aS,8R,8aS)-2-benzyl-3-hydroxy-5-methyl-1-oxo-8-phenyl-2,3,4,4a,7,8-hexahydroisoquinoline-8a(1H)-carbonitrile

1609623-89-3

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Basic information

Product Name: (3S,4aS,8R,8aS)-2-benzyl-3-hydroxy-5-methyl-1-oxo-8-phenyl-2,3,4,4a,7,8-hexahydroisoquinoline-8a(1H)-carbonitrile
Synonyms: (3S,4aS,8R,8aS)-2-benzyl-3-hydroxy-5-methyl-1-oxo-8-phenyl-2,3,4,4a,7,8-hexahydroisoquinoline-8a(1H)-carbonitrile
CAS NO:1609623-89-3
Molecular Formula:
Molecular Weight: 372.467
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: (3S,4aS,8R,8aS)-2-benzyl-3-hydroxy-5-methyl-1-oxo-8-phenyl-2,3,4,4a,7,8-hexahydroisoquinoline-8a(1H)-carbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: (3S,4aS,8R,8aS)-2-benzyl-3-hydroxy-5-methyl-1-oxo-8-phenyl-2,3,4,4a,7,8-hexahydroisoquinoline-8a(1H)-carbonitrile(1609623-89-3)
EPA Substance Registry System: (3S,4aS,8R,8aS)-2-benzyl-3-hydroxy-5-methyl-1-oxo-8-phenyl-2,3,4,4a,7,8-hexahydroisoquinoline-8a(1H)-carbonitrile(1609623-89-3)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1609623-89-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1609623-89-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,9,6,2 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1609623-89:
(9*1)+(8*6)+(7*0)+(6*9)+(5*6)+(4*2)+(3*3)+(2*8)+(1*9)=183
183 % 10 = 3
So 1609623-89-3 is a valid CAS Registry Number.

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1609623-89-3Relevant academic research and scientific papers

Organocatalytic cascade reactions: Diversity-oriented synthesis for the construction of hydroisoquinoline scaffolds

Gómez, Clarisa Villegas,Cruz, David Cruz,Mose, Rasmus,J?rgensen, Karl Anker

supporting information, p. 6035 - 6038 (2014/05/20)

The organocatalytic enantioselective synthesis of highly functionalized hydroisoquinolines by trienamine-mediated [4+2]-cycloaddition/nucleophilic ring-closing reaction cascade sequence of cyanoacrylamides with 2,4-dienals is presented. The corresponding cycloadducts are formed in high yields and excellent stereoselectivities. Moreover, a series of transformations demonstrate the synthetic application of the obtained hydroisoquinolines. the Partner Organisations 2014.

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