Cas 132664-74-5,(2R,3R,10bS)-3-Benzoyl-2-(3-fluoro-phenyl)-2,3-dihydro-10bH-pyrrolo[2,1-a]isoquinoline-1,1-dicarbonitrile

132664-74-5

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Basic information

Product Name: (2R,3R,10bS)-3-Benzoyl-2-(3-fluoro-phenyl)-2,3-dihydro-10bH-pyrrolo[2,1-a]isoquinoline-1,1-dicarbonitrile
Synonyms: (2R,3R,10bS)-3-Benzoyl-2-(3-fluoro-phenyl)-2,3-dihydro-10bH-pyrrolo[2,1-a]isoquinoline-1,1-dicarbonitrile
CAS NO:132664-74-5
Molecular Formula:
Molecular Weight: 419.458
EINECS: N/A
Product Categories: N/A
Mol File: 132664-74-5.mol
Article Data: 1

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: (2R,3R,10bS)-3-Benzoyl-2-(3-fluoro-phenyl)-2,3-dihydro-10bH-pyrrolo[2,1-a]isoquinoline-1,1-dicarbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R,10bS)-3-Benzoyl-2-(3-fluoro-phenyl)-2,3-dihydro-10bH-pyrrolo[2,1-a]isoquinoline-1,1-dicarbonitrile(132664-74-5)
EPA Substance Registry System: (2R,3R,10bS)-3-Benzoyl-2-(3-fluoro-phenyl)-2,3-dihydro-10bH-pyrrolo[2,1-a]isoquinoline-1,1-dicarbonitrile(132664-74-5)

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: 132664-74-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 132664-74-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,6,6 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 132664-74:
(8*1)+(7*3)+(6*2)+(5*6)+(4*6)+(3*4)+(2*7)+(1*4)=125
125 % 10 = 5
So 132664-74-5 is a valid CAS Registry Number.

132664-74-5Upstream product

2972-71-6 3-fluorobenzylidenemalononitrile

132664-74-5Downstream Products

132664-74-5Relevant articles and documents

REGIO- AND STEREODIRECTIVITY IN THE REACTIONS OF ISOQUINOLINIUM YLIDES WITH UNSATURATED NITRILES

Shestopalov, A. M.,Rodinovskaya, L. A.,Sharanin, Yu. A.,Litvinov, V. P.

, p. 2348 - 2353 (2007/10/02)

Reactions of isoquinolinium ylides with arylmethylenemalonitriles involve 1,3-dipolar cycloaddition, with the highly regio- and stereoselective formation of 2-aryl-3-benzoyl(or carbamoyl)-1,1-dicyano-2,3-trans-1,2,3,10b-tetrahydropyrroloisoquinolines.In contrast, N-phenacylisoquinolinium ylide reacts with arylmethylenecyanothioacetamides differently, proceeding regio- and stereoselectively to give 4-aryl-2-hydroxy-3-(1-isoquinolinio)-2-phenyl-3-cyano-3,4-trans-1,2,3,4-tetrahydropyridine-6-thiolates.

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