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(R)-1-[(4-Chlorophenyl)phenylmethyl]piperazine

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(R)-1-[(4-Chlorophenyl)phenylmethyl]piperazine Basic information

Product Name:
(R)-1-[(4-Chlorophenyl)phenylmethyl]piperazine
Synonyms:
  • (-)-1-[(4-CHLOROPHENYL)PHENYLMETHYL]PIPERAZINE
  • Levocetirizine Impurity 2
  • (R)-(-)-1-[(4-Chlorophenyl)phenylmethyl]piperazine
  • (R)-1-(p-Chlorobenzhydryl)piperazine
  • Piperazine,1-[(R)-(4-chlorophenyl)phenylMethyl]-
  • (R)-1-[^a-(4-Chlorophenyl)benzyl]piperazine, 97%
  • (R)-1-[alpha-(4-Chlorophenyl)benzyl]piperazine
  • Levocetirizine Impurity A
CAS:
300543-56-0
MF:
C17H19ClN2
MW:
286.8
EINECS:
608-439-5
Product Categories:
  • Aromatics
  • Chiral Reagents
  • Pharmaceutical Intermediates
  • Heterocycles
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
Mol File:
300543-56-0.mol
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(R)-1-[(4-Chlorophenyl)phenylmethyl]piperazine Chemical Properties

Melting point:
91-93oC
Boiling point:
409.1±0.0 °C(Predicted)
Density 
1.158
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
Chloroform (Slightly), Dichloromethane (Slightly), Methanol (Slightly)
pka
8.99±0.10(Predicted)
form 
Solid
color 
White
PH
9.38 at 25℃ and 10.07g/L
Water Solubility 
Soluble in chloroform, methanol, and dichloromethane. Slightly soluble in water.
InChI
InChI=1/C17H19ClN2/c18-16-8-6-15(7-9-16)17(14-4-2-1-3-5-14)20-12-10-19-11-13-20/h1-9,17,19H,10-13H2/t17-/s3
InChIKey
UZKBSZSTDQSMDR-SCBJWRGWNA-N
SMILES
[C@@H](N1CCNCC1)(C1C=CC=CC=1)C1C=CC(Cl)=CC=1 |&1:0,r|
CAS DataBase Reference
300543-56-0
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Safety Information

HS Code 
2933599550
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(R)-1-[(4-Chlorophenyl)phenylmethyl]piperazine Usage And Synthesis

Uses

Intermediate in the production of (R)-Cetirizine (C281106).

Uses

(R)-1-[alpha-(4-Chlorophenyl)benzyl]piperazine intermediate in the production of (R)-Cetirizine.

Application

(R)-1-[(4-Chlorophenyl)phenylmethyl]piperazine could be used to synthesize a series of novel derivatives. Most of these derivatives significantly affected both allergic asthma and allergic itching. Meanwhile, in the test of allergic itching, five of the 19 compounds have more potent activities than levocetirizine[1].

References

[1] Lisheng Wang. “Design, synthesis, and anti-allergic activities of novel (R)(-)-1-[(4-chlorophenyl)phenyl methyl]piperazine derivatives.” Medicinal Chemistry Research 21 1 (2010): 124–132.

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