Cas 1334433-03-2,(1R,2S,4S)-2-isopropyl-4-methylcyclohexyl (3aR,4aS,10bR)-6-oxo-3,3a,4,4a-tetrahydro-2H-furo[2',3':2,3]cyclobuta[1,2-c]isoquinoline-5(6H)-carboxylate

1334433-03-2

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Basic information

Product Name: (1R,2S,4S)-2-isopropyl-4-methylcyclohexyl (3aR,4aS,10bR)-6-oxo-3,3a,4,4a-tetrahydro-2H-furo[2',3':2,3]cyclobuta[1,2-c]isoquinoline-5(6H)-carboxylate
Synonyms: (1R,2S,4S)-2-isopropyl-4-methylcyclohexyl (3aR,4aS,10bR)-6-oxo-3,3a,4,4a-tetrahydro-2H-furo[2',3':2,3]cyclobuta[1,2-c]isoquinoline-5(6H)-carboxylate
CAS NO:1334433-03-2
Molecular Formula:
Molecular Weight: 397.514
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: (1R,2S,4S)-2-isopropyl-4-methylcyclohexyl (3aR,4aS,10bR)-6-oxo-3,3a,4,4a-tetrahydro-2H-furo[2',3':2,3]cyclobuta[1,2-c]isoquinoline-5(6H)-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2S,4S)-2-isopropyl-4-methylcyclohexyl (3aR,4aS,10bR)-6-oxo-3,3a,4,4a-tetrahydro-2H-furo[2',3':2,3]cyclobuta[1,2-c]isoquinoline-5(6H)-carboxylate(1334433-03-2)
EPA Substance Registry System: (1R,2S,4S)-2-isopropyl-4-methylcyclohexyl (3aR,4aS,10bR)-6-oxo-3,3a,4,4a-tetrahydro-2H-furo[2',3':2,3]cyclobuta[1,2-c]isoquinoline-5(6H)-carboxylate(1334433-03-2)

Safety Data

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Safety Statements: N/A
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RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1334433-03-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1334433-03-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,4,4,3 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1334433-03:
(9*1)+(8*3)+(7*3)+(6*4)+(5*4)+(4*3)+(3*3)+(2*0)+(1*3)=122
122 % 10 = 2
So 1334433-03-2 is a valid CAS Registry Number.

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1334433-03-2Relevant academic research and scientific papers

Intramolecular [2+2] photocycloaddition of substituted isoquinolones: Enantioselectivity and kinetic resolution induced by a chiral template

Austin, Kerrie A. B.,Herdtweck, Eberhardt,Bach, Thorsten

, p. 8416 - 8419 (2011/10/31)

From simple to complex: Starting from easily accessible isoquinolones 1 (X=Br, OH), complex cyclobutane photoproducts such as compound 2 can be obtained with high enantioselectivity (88-96% ee) through the use of a chiral template. Compound 3, which was i

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