Cas 142730-58-3,Acetic acid 1-hydroxymethyl-2-(4-phenyl-piperazin-1-yl)-ethyl ester

142730-58-3

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Basic information

Product Name: Acetic acid 1-hydroxymethyl-2-(4-phenyl-piperazin-1-yl)-ethyl ester
Synonyms: Acetic acid 1-hydroxymethyl-2-(4-phenyl-piperazin-1-yl)-ethyl ester
CAS NO:142730-58-3
Molecular Formula:
Molecular Weight: 278.351
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: Acetic acid 1-hydroxymethyl-2-(4-phenyl-piperazin-1-yl)-ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid 1-hydroxymethyl-2-(4-phenyl-piperazin-1-yl)-ethyl ester(142730-58-3)
EPA Substance Registry System: Acetic acid 1-hydroxymethyl-2-(4-phenyl-piperazin-1-yl)-ethyl ester(142730-58-3)

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: 142730-58-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 142730-58-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,7,3 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 142730-58:
(8*1)+(7*4)+(6*2)+(5*7)+(4*3)+(3*0)+(2*5)+(1*8)=113
113 % 10 = 3
So 142730-58-3 is a valid CAS Registry Number.

142730-58-3Upstream product

142730-57-2 (R,S)-3-(4-phenyl-1-piperazinyl)-1,2-propanediol diacetate

142730-58-3Downstream Products

142730-58-3Relevant academic research and scientific papers

Enzymatic resolution of 1,2-diols: Preparation of optically pure dropropizine

Bianchi,Bosetti,Cesti,Golini

, p. 3231 - 3234 (1992)

Kinetic resolution of (R,S)-3-(4-phenyl-1-piperazinyl)-1,2-propranediol diacetate (2) by alcoholysis with n-propanol was carried out under lipase Amano PS catalysis in various organic solvents. Pure enantiomers of the corresponding diol (1) are useful as antitussive and central sedative therapeutic agents.

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