Cas 1153630-87-5,(S)-1-{3-[4-(2-ethoxyphenyl)piperazin-1-yl]-2-hydroxypropyl}-pyrrolidin-2-one

1153630-87-5

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Basic information

Product Name: (S)-1-{3-[4-(2-ethoxyphenyl)piperazin-1-yl]-2-hydroxypropyl}-pyrrolidin-2-one
Synonyms: (S)-1-{3-[4-(2-ethoxyphenyl)piperazin-1-yl]-2-hydroxypropyl}-pyrrolidin-2-one
CAS NO:1153630-87-5
Molecular Formula:
Molecular Weight: 347.458
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: (S)-1-{3-[4-(2-ethoxyphenyl)piperazin-1-yl]-2-hydroxypropyl}-pyrrolidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (S)-1-{3-[4-(2-ethoxyphenyl)piperazin-1-yl]-2-hydroxypropyl}-pyrrolidin-2-one(1153630-87-5)
EPA Substance Registry System: (S)-1-{3-[4-(2-ethoxyphenyl)piperazin-1-yl]-2-hydroxypropyl}-pyrrolidin-2-one(1153630-87-5)

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: 1153630-87-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1153630-87-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,3,6,3 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1153630-87:
(9*1)+(8*1)+(7*5)+(6*3)+(5*6)+(4*3)+(3*0)+(2*8)+(1*7)=135
135 % 10 = 5
So 1153630-87-5 is a valid CAS Registry Number.

1153630-87-5Upstream product

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1153630-87-5Relevant academic research and scientific papers

Application of cyclic sulfates in the synthesis of enantiomers of 1-[3-(4-aryl-piperazin-1-yl)-2-hydroxy-propyl]-pyrrolidin-2-one

Kulig, Katarzyna,Boba, Agnieszka,Bielejewska, Anna,Gorska, Magdalena,Malawska, Barbara

, p. 322 - 326 (2009)

The synthesis of enantiomers of 1-[3-(4-aryl-piperazin-1-yl)-2-hydroxy-propyl]-pyrrolidin-2-one derivatives is described. These enantiomers were synthesized starting from (R)- or (S)-1-chloro-2,3-dihydroxypropane using relevant cyclic sulfates as chiral i

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