Cas 129355-67-5,ETHYL 2-[1-(2,6-DIFLUOROBENZOYL)-3-OXO-2-PIPERAZINYL]ACETATE

129355-67-5

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Basic information

Product Name: ETHYL 2-[1-(2,6-DIFLUOROBENZOYL)-3-OXO-2-PIPERAZINYL]ACETATE
Synonyms: ETHYL 2-[1-(2,6-DIFLUOROBENZOYL)-3-OXO-2-PIPERAZINYL]ACETATE;ethyl 2-[1-(2,6-difluorobenzoyl)-3-oxopiperazin-2-yl]acetate
CAS NO:129355-67-5
Molecular Formula: C₁₅H₁₆F₂N₂O₄
Molecular Weight: 326.3
EINECS: N/A
Product Categories: N/A
Mol File: 129355-67-5.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: ETHYL 2-[1-(2,6-DIFLUOROBENZOYL)-3-OXO-2-PIPERAZINYL]ACETATE(CAS DataBase Reference)
NIST Chemistry Reference: ETHYL 2-[1-(2,6-DIFLUOROBENZOYL)-3-OXO-2-PIPERAZINYL]ACETATE(129355-67-5)
EPA Substance Registry System: ETHYL 2-[1-(2,6-DIFLUOROBENZOYL)-3-OXO-2-PIPERAZINYL]ACETATE(129355-67-5)

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: 129355-67-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 129355-67-5 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, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 129355-67:
(8*1)+(7*2)+(6*9)+(5*3)+(4*5)+(3*5)+(2*6)+(1*7)=145
145 % 10 = 5
So 129355-67-5 is a valid CAS Registry Number.

129355-67-5Upstream product

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129355-67-5Relevant articles and documents

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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