Cas 1000669-30-6,(S)-1-[3-[4-(2-chlorophenyl)piperazin-1-yl]-2-hydroxypropyl]pyrrolidin-2-one

1000669-30-6

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Basic information

Product Name: (S)-1-[3-[4-(2-chlorophenyl)piperazin-1-yl]-2-hydroxypropyl]pyrrolidin-2-one
Synonyms: (S)-1-[3-[4-(2-chlorophenyl)piperazin-1-yl]-2-hydroxypropyl]pyrrolidin-2-one
CAS NO:1000669-30-6
Molecular Formula:
Molecular Weight: 337.849
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-chlorophenyl)piperazin-1-yl]-2-hydroxypropyl]pyrrolidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (S)-1-[3-[4-(2-chlorophenyl)piperazin-1-yl]-2-hydroxypropyl]pyrrolidin-2-one(1000669-30-6)
EPA Substance Registry System: (S)-1-[3-[4-(2-chlorophenyl)piperazin-1-yl]-2-hydroxypropyl]pyrrolidin-2-one(1000669-30-6)

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: 1000669-30-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1000669-30-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,0,6,6 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1000669-30:
(9*1)+(8*0)+(7*0)+(6*0)+(5*6)+(4*6)+(3*9)+(2*3)+(1*0)=96
96 % 10 = 6
So 1000669-30-6 is a valid CAS Registry Number.

1000669-30-6Upstream product

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1000669-30-6Relevant 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

experimental part, p. 322 - 326 (2009/09/05)

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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