Cas 338797-22-1,2-methyl-4-(6-nitro-quinolin-4-yl)-piperazine-1-carboxylic acid <i>tert</i>-butyl ester

338797-22-1

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Basic information

Product Name: 2-methyl-4-(6-nitro-quinolin-4-yl)-piperazine-1-carboxylic acid tert-butyl ester
Synonyms: 2-methyl-4-(6-nitro-quinolin-4-yl)-piperazine-1-carboxylic acid tert-butyl ester
CAS NO:338797-22-1
Molecular Formula:
Molecular Weight: 372.424
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-methyl-4-(6-nitro-quinolin-4-yl)-piperazine-1-carboxylic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-methyl-4-(6-nitro-quinolin-4-yl)-piperazine-1-carboxylic acid tert-butyl ester(338797-22-1)
EPA Substance Registry System: 2-methyl-4-(6-nitro-quinolin-4-yl)-piperazine-1-carboxylic acid tert-butyl ester(338797-22-1)

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: 338797-22-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 338797-22-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,8,7,9 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 338797-22:
(8*3)+(7*3)+(6*8)+(5*7)+(4*9)+(3*7)+(2*2)+(1*2)=191
191 % 10 = 1
So 338797-22-1 is a valid CAS Registry Number.

338797-22-1Upstream product

75336-86-6 (2R)-methylpiperazine

338797-22-1Downstream Products

338797-22-1Relevant academic research and scientific papers

Novel (4-piperazin-1-ylquinolin-6-yl) arylsulfonamides with high affinity and selectivity for the 5-HT(6) receptor.

Bromidge,Griffith,Heightman,Jennings,King,Moss,Newman,Riley,Routledge,Serafinowska,Thomas

, p. 2843 - 2846 (2007/10/03)

The discovery of (4-piperazin-1-ylquinolin-6-yl) arylsulfonamides and their binding affinities for a selection of 5-HT and dopamine subreceptors is described. Many compounds show high affinity (pK(i)>8) for the 5-HT(6) receptor and >100-fold selectivity against a range of other receptors. Structure-activity relationships of these compounds are discussed.

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