Cas 211820-01-8,Piperazine, 1-[[4-[(4-fluorophenyl)sulfonyl]-1-piperazinyl]carbonyl]-4-(4-pyridinyl)-

211820-01-8

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Basic information

Product Name: Piperazine, 1-[[4-[(4-fluorophenyl)sulfonyl]-1-piperazinyl]carbonyl]-4-(4-pyridinyl)-
Synonyms:
CAS NO:211820-01-8
Molecular Formula: C20H24FN5O3S
Molecular Weight: 433.507
EINECS: N/A
Product Categories: N/A
Mol File: 211820-01-8.mol
Article Data: 2

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: Piperazine, 1-[[4-[(4-fluorophenyl)sulfonyl]-1-piperazinyl]carbonyl]-4-(4-pyridinyl)-(CAS DataBase Reference)
NIST Chemistry Reference: Piperazine, 1-[[4-[(4-fluorophenyl)sulfonyl]-1-piperazinyl]carbonyl]-4-(4-pyridinyl)-(211820-01-8)
EPA Substance Registry System: Piperazine, 1-[[4-[(4-fluorophenyl)sulfonyl]-1-piperazinyl]carbonyl]-4-(4-pyridinyl)-(211820-01-8)

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: 211820-01-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 211820-01-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,1,8,2 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 211820-01:
(8*2)+(7*1)+(6*1)+(5*8)+(4*2)+(3*0)+(2*0)+(1*1)=78
78 % 10 = 8
So 211820-01-8 is a valid CAS Registry Number.

211820-01-8Upstream product

1008-91-9 4-(piperazin-1-yl)pyridine

211820-01-8Downstream Products

211820-01-8Relevant articles and documents

Novel 4-piperidinopyridine inhibitors of oxidosqualene cyclase-lanosterol synthase derived by consideration of inhibitor pKa

Brown, George R.,Foubister, Alan J.,Johnson, Michael C.,Newcombe, Nicholas J.,Waterson, David,Wells, Stuart L.

, p. 2213 - 2216 (2001)

Potent inhibition of rat microsomal oxidosqualene cyclase-lanosterol synthase (OSC) was maintained after structural modification of the 4-piperidinopyridine OSC inhibitor series. These novel analogues with a much lower pKa range (5.8-6.7) gave

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