Cas 343240-82-4,4-[[7-(3,4-Dichlorophenyl)-4,7-dihydro-5-methyl-pyrazolo[1,5-a]pyrimidin-6-yl]carbonyl]morpholine

343240-82-4

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Basic information

Product Name: 4-[[7-(3,4-Dichlorophenyl)-4,7-dihydro-5-methyl-pyrazolo[1,5-a]pyrimidin-6-yl]carbonyl]morpholine
Synonyms:
CAS NO:343240-82-4
Molecular Formula:
Molecular Weight: 393.273
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-[[7-(3,4-Dichlorophenyl)-4,7-dihydro-5-methyl-pyrazolo[1,5-a]pyrimidin-6-yl]carbonyl]morpholine(CAS DataBase Reference)
NIST Chemistry Reference: 4-[[7-(3,4-Dichlorophenyl)-4,7-dihydro-5-methyl-pyrazolo[1,5-a]pyrimidin-6-yl]carbonyl]morpholine(343240-82-4)
EPA Substance Registry System: 4-[[7-(3,4-Dichlorophenyl)-4,7-dihydro-5-methyl-pyrazolo[1,5-a]pyrimidin-6-yl]carbonyl]morpholine(343240-82-4)

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: 343240-82-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 343240-82-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,3,2,4 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 343240-82:
(8*3)+(7*4)+(6*3)+(5*2)+(4*4)+(3*0)+(2*8)+(1*2)=114
114 % 10 = 4
So 343240-82-4 is a valid CAS Registry Number.

343240-82-4Upstream product

343240-82-4Downstream Products

343240-82-4Relevant academic research and scientific papers

Dihydropyrazolopyrimidine Inhibitors of KV1.5 (IKur)

Vaccaro, Wayne,Huynh, Tram,Lloyd, John,Atwal, Karnail,Finlay, Heather J.,Levesque, Paul,Conder, Mary Lee,Jenkins-West, Tonya,Shi, Hong,Sun, Lucy

experimental part, p. 6381 - 6385 (2009/09/06)

A series of dihydropyrazolopyrimidine inhibitors of KV1.5 (IKur) have been identified. The synthesis, structure-activity relationships and selectivity against several other ion channels are described.

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