Cas 1265227-48-2,(R,S)-2-[4-(bis(4-fluorophenyl)methyl)piperazin-1-yl]-N-(2-fluorobenzyl)-4-hydroxybutanamide

1265227-48-2

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Basic information

Product Name: (R,S)-2-[4-(bis(4-fluorophenyl)methyl)piperazin-1-yl]-N-(2-fluorobenzyl)-4-hydroxybutanamide
Synonyms: (R,S)-2-[4-(bis(4-fluorophenyl)methyl)piperazin-1-yl]-N-(2-fluorobenzyl)-4-hydroxybutanamide
CAS NO:1265227-48-2
Molecular Formula:
Molecular Weight: 497.56
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: (R,S)-2-[4-(bis(4-fluorophenyl)methyl)piperazin-1-yl]-N-(2-fluorobenzyl)-4-hydroxybutanamide(CAS DataBase Reference)
NIST Chemistry Reference: (R,S)-2-[4-(bis(4-fluorophenyl)methyl)piperazin-1-yl]-N-(2-fluorobenzyl)-4-hydroxybutanamide(1265227-48-2)
EPA Substance Registry System: (R,S)-2-[4-(bis(4-fluorophenyl)methyl)piperazin-1-yl]-N-(2-fluorobenzyl)-4-hydroxybutanamide(1265227-48-2)

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: 1265227-48-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1265227-48-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,5,2,2 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1265227-48:
(9*1)+(8*2)+(7*6)+(6*5)+(5*2)+(4*2)+(3*7)+(2*4)+(1*8)=152
152 % 10 = 2
So 1265227-48-2 is a valid CAS Registry Number.

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1265227-48-2Relevant academic research and scientific papers

Synthesis and biological evaluation of new derivatives of 2-substituted 4-hydroxybutanamides as GABA uptake inhibitors

Kulig, Katarzyna,Wickowski, Krzysztof,Wickowska, Anna,Gajda, Justyna,Pochwat, Bart?omiej,H?fner, Georg C.,Wanner, Klaus T.,Malawska, Barbara

, p. 183 - 190 (2011)

This study presents the synthesis of novel substituted 4-hydroxybutanamides and their influence on the activity of murine GABA transport proteins GAT1-GAT4. The active compounds, derivatives of N-arylalkyl-2-(4- diphenylmethylpiperazin-1-yl)-4-hydroxybuty

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