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1-(CHLOROACETYL)-4-(4-NITROPHENYL)PIPERAZINE, also known as CAPNP, is a chemical compound characterized by a piperazine ring with a chloroacetyl and nitrophenyl group attached. Its unique structure and properties make it a promising candidate for pharmaceutical research and development, targeting a range of disorders and serving as a reagent in organic synthesis.

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  • 16264-11-2 Structure
  • Basic information

    1. Product Name: 1-(CHLOROACETYL)-4-(4-NITROPHENYL)PIPERAZINE
    2. Synonyms: 2-Chloro-1-(4-(4-nitrophenyl)piperazin-1-yl)ethanone;Ethanone,2-chloro-1-[4-(4-nitrophenyl)-1-piperazinyl]-;2-chloro-1-[4-(4-nitrophenyl)-1-piperazinyl]ethanone
    3. CAS NO:16264-11-2
    4. Molecular Formula: C12H14ClN3O3
    5. Molecular Weight: 283.72
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 16264-11-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 504°Cat760mmHg
    3. Flash Point: 258.6°C
    4. Appearance: /
    5. Density: 1.368g/cm3
    6. Vapor Pressure: 2.76E-10mmHg at 25°C
    7. Refractive Index: 1.597
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 1.35±0.10(Predicted)
    11. CAS DataBase Reference: 1-(CHLOROACETYL)-4-(4-NITROPHENYL)PIPERAZINE(CAS DataBase Reference)
    12. NIST Chemistry Reference: 1-(CHLOROACETYL)-4-(4-NITROPHENYL)PIPERAZINE(16264-11-2)
    13. EPA Substance Registry System: 1-(CHLOROACETYL)-4-(4-NITROPHENYL)PIPERAZINE(16264-11-2)
  • 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: 16264-11-2(Hazardous Substances Data)

16264-11-2 Usage

Uses

Used in Pharmaceutical Research and Development:
1-(CHLOROACETYL)-4-(4-NITROPHENYL)PIPERAZINE is used as a potential therapeutic agent for the treatment of various disorders, including schizophrenia, depression, and anxiety. Its chemical structure allows for the modulation of specific biological pathways and receptors, offering new avenues for drug discovery and development.
Used in Organic Synthesis:
1-(CHLOROACETYL)-4-(4-NITROPHENYL)PIPERAZINE is used as a reagent in organic synthesis, facilitating the formation of new chemical compounds and contributing to the advancement of chemical research.
Used in Chemical Production:
1-(CHLOROACETYL)-4-(4-NITROPHENYL)PIPERAZINE is used as an intermediate in the production of other chemical compounds, playing a crucial role in the synthesis of various pharmaceuticals and specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 16264-11-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,2,6 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 16264-11:
(7*1)+(6*6)+(5*2)+(4*6)+(3*4)+(2*1)+(1*1)=92
92 % 10 = 2
So 16264-11-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H14ClN3O3/c13-9-12(17)15-7-5-14(6-8-15)10-1-3-11(4-2-10)16(18)19/h1-4H,5-9H2

16264-11-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-1-[4-(4-nitrophenyl)piperazin-1-yl]ethanone

1.2 Other means of identification

Product number -
Other names 2-chloro-1-<4-(4-nitrophenyl)piperazin-1-yl>acetamide

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:16264-11-2 SDS

16264-11-2Relevant articles and documents

Design, synthesis and biological profiling of aryl piperazine based scaffolds for the management of androgen sensitive prostatic disorders

Gupta, Sonal,Pandey, Deepti,Mandalapu, Dhanaraju,Bala, Veenu,Sharma, Vikas,Shukla, Mahendra,Yadav, Santosh K.,Singh, Nidhi,Jaiswal, Swati,Maikhuri, Jagdamba P.,Lal, Jawahar,Siddiqi, Mohammad I.,Gupta, Gopal,Sharma, Vishnu L.

supporting information, p. 2111 - 2121 (2016/11/18)

In the quest for novel scaffolds for the management of androgen sensitive prostatic disorders like prostate cancer and benign prostatic hyperplasia, a series of twenty-six aryl/heteroaryl piperazine derivatives have been described. Three compounds, 8a, 8c

Synthesis and serotonergic activity of arylpiperazide derivatives of serotonin: Potent agonists for 5-HT(1D) receptors

Perez,Fourrier,Sigogneau,Pauwels,Palmier,John,Valentin,Halazy

, p. 3602 - 3607 (2007/10/03)

A series of new arylpiperazide derivatives of serotonin has been prepared and evaluated as 5-HT(1D) receptor agonists. Binding experiments at cloned human 5-HT(1Dα), 5-HT(1Dβ), and 5-HT(1A) receptors show that all the compounds are very potent and selecti

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