ChemicalBook > Product Catalog > Organic Chemistry > Nitrogen Compounds > (R)-1-[(4-Chlorophenyl)phenylmethyl]piperazine
(R)-1-[(4-Chlorophenyl)phenylmethyl]piperazine
(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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(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.
(R)-1-[(4-Chlorophenyl)phenylmethyl]piperazineSupplier
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