Cas 1342886-26-3,(S)-4-{(E)-2-[5-(3-fluorophenyl)pyridin-2-yl]vinyl}-7-hydroxy-2-methylhexahydro-pyrrolo[3,4-a]pyrrolizine-1,3-dione

1342886-26-3

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Basic information

Product Name: (S)-4-{(E)-2-[5-(3-fluorophenyl)pyridin-2-yl]vinyl}-7-hydroxy-2-methylhexahydro-pyrrolo[3,4-a]pyrrolizine-1,3-dione
Synonyms:
CAS NO:1342886-26-3
Molecular Formula:
Molecular Weight: 407.444
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: (S)-4-{(E)-2-[5-(3-fluorophenyl)pyridin-2-yl]vinyl}-7-hydroxy-2-methylhexahydro-pyrrolo[3,4-a]pyrrolizine-1,3-dione(CAS DataBase Reference)
NIST Chemistry Reference: (S)-4-{(E)-2-[5-(3-fluorophenyl)pyridin-2-yl]vinyl}-7-hydroxy-2-methylhexahydro-pyrrolo[3,4-a]pyrrolizine-1,3-dione(1342886-26-3)
EPA Substance Registry System: (S)-4-{(E)-2-[5-(3-fluorophenyl)pyridin-2-yl]vinyl}-7-hydroxy-2-methylhexahydro-pyrrolo[3,4-a]pyrrolizine-1,3-dione(1342886-26-3)

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: 1342886-26-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1342886-26-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,2,8,8 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1342886-26:
(9*1)+(8*3)+(7*4)+(6*2)+(5*8)+(4*8)+(3*6)+(2*2)+(1*6)=173
173 % 10 = 3
So 1342886-26-3 is a valid CAS Registry Number.

1342886-26-3Upstream product

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1342886-26-3Relevant academic research and scientific papers

TRICYCLIC PYRIDYL-VINYL PYRROLES AS PAR1 INHIBITORS

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Paragraph 0179-0185, (2013/03/26)

This disclosure relates to compounds of formula I: wherein R1, R2, R3, R4, X and Y have the meanings denoted in the disclosure. The compounds of formula I have antithrombotic activity and in particular inhibit the protease-activated receptor 1 (PAR1). The disclosure further relates to a method for producing the compound of formula I and to the use thereof as a pharmaceutical product.

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