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1-(Tetrahydro-2-furoyl)piperazine

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1-(Tetrahydro-2-furoyl)piperazine Basic information

Product Name:
1-(Tetrahydro-2-furoyl)piperazine
Synonyms:
  • RARECHEM AH CK 0199
  • (TETRAHYDROFURAN-2-YL)(PIPERAZIN-1-YL)METHANONE
  • N-(2-TETRAHYDROFUROYL)PIPERAZINE
  • N-(TETRAHYDRO-2-FUROYL)-PIPERAZINE
  • PIPERAZIN-1-YL-(TETRAHYDRO-FURAN-2-YL)-METHANONE
  • TIMTEC-BB SBB005794
  • 1-(2-TETRAHYDROFUROYL)-PIPERAZINE
  • 1-(TETRAHYDRO-2-FUROYL)PIPERAZINE
CAS:
63074-07-7
MF:
C9H16N2O2
MW:
184.24
EINECS:
613-137-1
Product Categories:
  • API intermediates
  • PHARMACEUTICAL INTERMEDIATES
Mol File:
63074-07-7.mol
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1-(Tetrahydro-2-furoyl)piperazine Chemical Properties

Boiling point:
140 °C (1.5002 mmHg)
Density 
1.17
refractive index 
1.5195-1.5215
Flash point:
120-125°C/0.2mm
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
Chloroform (Sparingly), Methanol (Slightly)
form 
Viscous Liquid
pka
8.37±0.10(Predicted)
color 
Colorless to yellow
Water Solubility 
Fully miscible in water.
BRN 
880578
InChI
1S/C9H16N2O2/c12-9(8-2-1-7-13-8)11-5-3-10-4-6-11/h8,10H,1-7H2
InChIKey
UKESBLFBQANJHH-UHFFFAOYSA-N
SMILES
O=C(C1CCCO1)N2CCNCC2
CAS DataBase Reference
63074-07-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38-36
Safety Statements 
37/39-26-37
WGK Germany 
3
Hazard Note 
Irritant
HS Code 
29349990
Storage Class
10 - Combustible liquids
Hazard Classifications
Eye Irrit. 2

MSDS

  • Language:English Provider:ACROS
  • Language:English Provider:ALFA
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1-(Tetrahydro-2-furoyl)piperazine Usage And Synthesis

Chemical Properties

colorless to yellow viscous liquid

Uses

1-?(Tetrahydro-?2-?furoyl)?-?piperazine (Terazosin EP Impurity N) has been used as a reactant for the preparation of pyrazol-3-propanoic acid derivatives as inhibitors of leukotriene biosynthesis in human neutrophils.

Definition

ChEBI: 1-(Tetrahydro-2-furoyl)piperazine is a member of phytanoyl-CoAs.

Synthesis

1-(Tetrahydro-2-furoyl)piperazine was prepared by using tetrahydrofurfuryl alcohol as the starting material, and the target compound tetrahydrofurfuryl piperazine was prepared by oxidizing tetrahydrofurfuryl acid, chlorinating to prepare acyl chloride and then acylating with piperazine.

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