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CAS

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301541-47-9

(R)-1-Benzyl-5-methylpiperazin-2-one is a chemical compound with the molecular formula C14H18N2O. It is a piperazinone derivative featuring a benzyl group and a methyl group attached to the piperazine ring. (R)-1-BENZYL-5-METHYLPIPERAZIN-2-ONE has potential applications in medicinal chemistry and drug development due to the diverse pharmacological activities of piperazinones.
Used in Pharmaceutical Industry:
(R)-1-Benzyl-5-methylpiperazin-2-one is used as a building block for the synthesis of various pharmaceutical compounds. Its unique structure allows it to be a key component in creating new and effective medications.
Used in Drug Development:
(R)-1-Benzyl-5-methylpiperazin-2-one serves as a starting material for the development of new drug candidates. Its potential biological and pharmacological effects make it a valuable asset in the discovery and design of innovative therapeutic agents.
Used in Medicinal Chemistry Research:
(R)-1-Benzyl-5-methylpiperazin-2-one is utilized in the study of structure-activity relationships in drug design. Understanding how its structure influences its activity can lead to the development of more potent and selective drugs.

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  • 301541-47-9 Structure

  • Basic information

    1. Product Name: (R)-1-BENZYL-5-METHYLPIPERAZIN-2-ONE
    2. Synonyms: (R)-1-BENZYL-5-METHYLPIPERAZIN-2-ONE;(5R)-5-Methyl-1-(phenylmethyl)-2-piperazinone;(5R)-1-Benzyl-5-methyl-piperazin-2-one
    3. CAS NO:301541-47-9
    4. Molecular Formula: C12H16N2O
    5. Molecular Weight: 204.27
    6. EINECS: N/A
    7. Product Categories: pharmacetical
    8. Mol File: 301541-47-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 380.9°Cat760mmHg
    3. Flash Point: 184.1°C
    4. Appearance: /
    5. Density: 1.084
    6. Vapor Pressure: 5.28E-06mmHg at 25°C
    7. Refractive Index: 1.543
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (R)-1-BENZYL-5-METHYLPIPERAZIN-2-ONE(CAS DataBase Reference)
    11. NIST Chemistry Reference: (R)-1-BENZYL-5-METHYLPIPERAZIN-2-ONE(301541-47-9)
    12. EPA Substance Registry System: (R)-1-BENZYL-5-METHYLPIPERAZIN-2-ONE(301541-47-9)

  • 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: 301541-47-9(Hazardous Substances Data)

301541-47-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 301541-47-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,1,5,4 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 301541-47:
(8*3)+(7*0)+(6*1)+(5*5)+(4*4)+(3*1)+(2*4)+(1*7)=89
89 % 10 = 9
So 301541-47-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H16N2O/c1-10-8-14(12(15)7-13-10)9-11-5-3-2-4-6-11/h2-6,10,13H,7-9H2,1H3/t10-/m1/s1

301541-47-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-1-BENZYL-5-METHYLPIPERAZIN-2-ONE

1.2 Other means of identification

Product number -
Other names (5R)-5-Methyl-1-(phenylmethyl)-2-piperazinone

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:301541-47-9 SDS

301541-47-9Downstream Products

301541-47-9Relevant articles and documents

Efficient synthesis of substituted piperazinones via tandem reductive amination-cyclization

Dinsmore,Zartman

, p. 6309 - 6312 (2007/10/03)

A new strategy for the preparation of substituted piperazinones features a tandem reductive coupling and S(N)2-cyclization of a 2-chloro-N-(2-oxoalkyl)acetamide (1) and a primary amine (2). The method is convenient for diversity-oriented synthesis, since a wide variety of amines may be used in the ring-forming reaction to produce N-substituted piperazinones (3). (C) 2000 Published by Elsevier science Ltd.

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