Cas 129355-73-3,[1-(2-Fluoro-benzoyl)-5,5-dimethyl-3-oxo-piperazin-2-yl]-acetic acid ethyl ester

129355-73-3

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Basic information

Product Name: [1-(2-Fluoro-benzoyl)-5,5-dimethyl-3-oxo-piperazin-2-yl]-acetic acid ethyl ester
Synonyms: [1-(2-Fluoro-benzoyl)-5,5-dimethyl-3-oxo-piperazin-2-yl]-acetic acid ethyl ester
CAS NO:129355-73-3
Molecular Formula:
Molecular Weight: 336.363
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: [1-(2-Fluoro-benzoyl)-5,5-dimethyl-3-oxo-piperazin-2-yl]-acetic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [1-(2-Fluoro-benzoyl)-5,5-dimethyl-3-oxo-piperazin-2-yl]-acetic acid ethyl ester(129355-73-3)
EPA Substance Registry System: [1-(2-Fluoro-benzoyl)-5,5-dimethyl-3-oxo-piperazin-2-yl]-acetic acid ethyl ester(129355-73-3)

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: 129355-73-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 129355-73-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,3,5 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 129355-73:
(8*1)+(7*2)+(6*9)+(5*3)+(4*5)+(3*5)+(2*7)+(1*3)=143
143 % 10 = 3
So 129355-73-3 is a valid CAS Registry Number.

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129355-73-3Relevant academic research and scientific papers

Synthesis and biological activity of a series of aspartate transcarbamoylase inhibitors: N-substituted diethyl aspartates and N-substituted-3-oxo-1,4-piperazine-2-acetic acid esters

Lal Dutta,Foye

, p. 447 - 452 (2007/10/02)

Series of N-substituted diethyl aspartates and N-substituted-3-oxo-1,4-piperazine-2-acetic acid esters were synthesized as potential inhibitors of aspartate transcarbamoylase. The aspartates were obtained by addition of substituted alkyl amines to diethyl

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