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832155-10-9

(R)-1-benzyl-3-phenylpiperazine, also known as (R)-BPP, is a chemical compound with the formula C18H22N2. It is a piperazine derivative and belongs to the class of phenylpiperazines, which are commonly used as psychoactive drugs and pharmaceutical intermediates. (R)-BPP has been studied for its potential use in the treatment of various neurological and psychiatric disorders, including depression and anxiety. It has also been investigated for its potential as a dopamine receptor agonist, and has shown promising results in preclinical studies. However, further research is needed to fully understand its effects and potential applications.

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  • 832155-10-9 Structure

  • Basic information

    1. Product Name: (R)-1-benzyl-3-phenylpiperazine
    2. Synonyms: (R)-1-benzyl-3-phenylpiperazine;(3R)-1-benzyl-3-phenylpiperazine;(3R)-3-Phenyl-1-(phenylmethyl)piperazine;(R)-3-Phenyl-1-(phenylmethyl)piperazine
    3. CAS NO:832155-10-9
    4. Molecular Formula: C17H20N2
    5. Molecular Weight: 252
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 832155-10-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.069
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (R)-1-benzyl-3-phenylpiperazine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-1-benzyl-3-phenylpiperazine(832155-10-9)
    11. EPA Substance Registry System: (R)-1-benzyl-3-phenylpiperazine(832155-10-9)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 832155-10-9(Hazardous Substances Data)

832155-10-9 Usage

Uses

Used in Pharmaceutical Industry:
(R)-BPP is used as a pharmaceutical intermediate for the development of psychoactive drugs, specifically targeting neurological and psychiatric disorders such as depression and anxiety. Its potential as a dopamine receptor agonist makes it a promising candidate for further research and development in this field.
Used in Research and Development:
(R)-BPP is used as a research compound to study its effects on dopamine receptors and its potential applications in treating various neurological and psychiatric disorders. Preclinical studies have shown promising results, and further research is necessary to understand its full potential and effects.

Check Digit Verification of cas no

The CAS Registry Mumber 832155-10-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,3,2,1,5 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 832155-10:
(8*8)+(7*3)+(6*2)+(5*1)+(4*5)+(3*5)+(2*1)+(1*0)=139
139 % 10 = 9
So 832155-10-9 is a valid CAS Registry Number.

832155-10-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-3-phenyl-1-(phenylmethyl)hexahydropyrazine

1.2 Other means of identification

Product number -
Other names (R)-N4-BENZYL-2-PHENYLPIPERAZINE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:832155-10-9 SDS

832155-10-9Upstream product

832155-10-9Downstream Products

832155-10-9Relevant articles and documents

Synthesis of Chiral Piperazines via Hydrogenation of Pyrazines Activated by Alkyl Halides

Huang, Wen-Xue,Liu, Lian-Jin,Wu, Bo,Feng, Guang-Shou,Wang, Baomin,Zhou, Yong-Gui

supporting information, p. 3082 - 3085 (2016/07/13)

A facile method has been developed for the synthesis of chiral piperazines through Ir-catalyzed hydrogenation of pyrazines activated by alkyl halides, giving a wide range of chiral piperazines including 3-substituted as well as 2,3- and 3,5-disubstituted

METHOD FOR PRODUCING OPTICALLY ACTIVE 2-ARYLPIPERAZINE DERIVATIVE

-

Page/Page column 21, (2009/12/05)

The objective of the present invention is to produce an optically active 2-arylpiperazine derivative useful as a synthetic intermediate for pharmaceutical products and agricultural chemicals from inexpensive and readily available starting material by an industrially practicable method. The objective can be accomplished by treating an optically active substituted aminodiol derivative produced from an optically active styrene oxide derivative with a sulfonating agent in the presence of a base, and then reacting an amine compound to obtain the 2-arylpiperazine derivative. Especially, an optically active 1-unsubstituted-2-arylpiperazine derivative can be produced by treating an optically active 1-allyl-2-arylpiperazine derivative with water in the presence of a transition metal catalyst for deallylation.

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