Cas 1310536-99-2,4-(3-chloro-5-(methylsulfonylcarbamoyl)pyridin-2-yl)-N-phenylpiperazine-1-carboxamide

1310536-99-2

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Basic information

Product Name: 4-(3-chloro-5-(methylsulfonylcarbamoyl)pyridin-2-yl)-N-phenylpiperazine-1-carboxamide
Synonyms: 4-(3-chloro-5-(methylsulfonylcarbamoyl)pyridin-2-yl)-N-phenylpiperazine-1-carboxamide
CAS NO:1310536-99-2
Molecular Formula:
Molecular Weight: 437.907
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: 4-(3-chloro-5-(methylsulfonylcarbamoyl)pyridin-2-yl)-N-phenylpiperazine-1-carboxamide(CAS DataBase Reference)
NIST Chemistry Reference: 4-(3-chloro-5-(methylsulfonylcarbamoyl)pyridin-2-yl)-N-phenylpiperazine-1-carboxamide(1310536-99-2)
EPA Substance Registry System: 4-(3-chloro-5-(methylsulfonylcarbamoyl)pyridin-2-yl)-N-phenylpiperazine-1-carboxamide(1310536-99-2)

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: 1310536-99-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1310536-99-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,0,5,3 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1310536-99:
(9*1)+(8*3)+(7*1)+(6*0)+(5*5)+(4*3)+(3*6)+(2*9)+(1*9)=122
122 % 10 = 2
So 1310536-99-2 is a valid CAS Registry Number.

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1310536-99-2Relevant academic research and scientific papers

A novel series of piperazinyl-pyridine ureas as antagonists of the purinergic P2Y12 receptor

Bach, Peter,Bostr?m, Jonas,Brickmann, Kay,Van Giezen,Hovland, Ragnar,Petersson, Annika U.,Ray, Asim,Zetterberg, Fredrik

supporting information; experimental part, p. 2877 - 2881 (2011/06/24)

A novel series of P2Y12 antagonists for development of drugs within the antiplatelet area is presented. The synthesis of the piperazinyl-pyridine urea derivatives and their structure-activity relationships (SAR) are described. Several compounds

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