Cas 582292-89-5,2-amino-4-(2,4-dichloro-phenyl)-6,7-dihydro-5H-benzo[6,7]cyclohepta[1,2-b]pyridine-3-carbonitrile

582292-89-5

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Basic information

Product Name: 2-amino-4-(2,4-dichloro-phenyl)-6,7-dihydro-5H-benzo[6,7]cyclohepta[1,2-b]pyridine-3-carbonitrile
Synonyms: 2-amino-4-(2,4-dichloro-phenyl)-6,7-dihydro-5H-benzo[6,7]cyclohepta[1,2-b]pyridine-3-carbonitrile
CAS NO:582292-89-5
Molecular Formula:
Molecular Weight: 380.276
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: 2-amino-4-(2,4-dichloro-phenyl)-6,7-dihydro-5H-benzo[6,7]cyclohepta[1,2-b]pyridine-3-carbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: 2-amino-4-(2,4-dichloro-phenyl)-6,7-dihydro-5H-benzo[6,7]cyclohepta[1,2-b]pyridine-3-carbonitrile(582292-89-5)
EPA Substance Registry System: 2-amino-4-(2,4-dichloro-phenyl)-6,7-dihydro-5H-benzo[6,7]cyclohepta[1,2-b]pyridine-3-carbonitrile(582292-89-5)

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: 582292-89-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 582292-89-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,8,2,2,9 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 582292-89:
(8*5)+(7*8)+(6*2)+(5*2)+(4*9)+(3*2)+(2*8)+(1*9)=185
185 % 10 = 5
So 582292-89-5 is a valid CAS Registry Number.

582292-89-5Upstream product

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582292-89-5Relevant academic research and scientific papers

Aminomethylpyridines as DPP-IV inhibitors

Peters, Jens-Uwe,Weber, Silja,Kritter, Stephane,Weiss, Peter,Wallier, Angelina,Zimmerli, Daniel,Boehringer, Markus,Steger, Matthias,Loeffler, Bernd-Michael

, p. 3579 - 3580 (2007/10/03)

In a novel series of DPP-IV inhibitors, a large increase of inhibitory activity was achieved by optimisation of aromatic substituents and conformational restriction.

Pyridine and quinoline derivatives

-

, (2008/06/13)

The present invention provides compounds of formula (I) wherein R1, R2, R3 and R4 are as defined in the specification, and pharmaceutically acceptable salts thereof. The compounds are useful for the treatment an

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