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132740-50-2

1-Cyclopentyl-4-aminopiperidine, with the CAS number 362745-67-7, is an organic compound that is widely recognized for its role in various chemical reactions. It features a piperidine base structure, which is a common component in numerous pharmaceutical drugs. 1-CYCLOPENTYL-4-AMINOPIPERIDINE is part of the piperidine class of organic compounds, known for their high reactivity and potential biological activity. It is utilized as a synthetic, specialty, and fine chemical in industrial applications. However, the specific properties, toxicity, environmental impacts, and safety measures of 1-Cyclopentyl-4-aminopiperidine are not extensively studied or well-defined, highlighting the importance of safety precautions during its handling or use in laboratory or industrial settings.

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  • 132740-50-2 Structure

  • Basic information

    1. Product Name: 1-CYCLOPENTYL-4-AMINOPIPERIDINE
    2. Synonyms: 1-CYCLOPENTYL-4-AMINOPIPERIDINE;1-cyclopentylpiperidin-4-amine(SALTDATA: 2HCl 2H2O);1-Cyclopentylpiperidin-4-aMine 2HCl;1-Cyclopentyl-4-piperidinamine
    3. CAS NO:132740-50-2
    4. Molecular Formula: C10H20N2
    5. Molecular Weight: 168.2792
    6. EINECS: 604-604-1
    7. Product Categories: Piperidine
    8. Mol File: 132740-50-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 230.8 °C at 760 mmHg
    3. Flash Point: 88.2 °C
    4. Appearance: /
    5. Density: 1.004 g/cm3
    6. Vapor Pressure: 0.0645mmHg at 25°C
    7. Refractive Index: 1.524
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. CAS DataBase Reference: 1-CYCLOPENTYL-4-AMINOPIPERIDINE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-CYCLOPENTYL-4-AMINOPIPERIDINE(132740-50-2)
    12. EPA Substance Registry System: 1-CYCLOPENTYL-4-AMINOPIPERIDINE(132740-50-2)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: 22-37/38-41
    3. Safety Statements: 26-39
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 132740-50-2(Hazardous Substances Data)

132740-50-2 Usage

Uses

Used in Pharmaceutical Industry:
1-Cyclopentyl-4-aminopiperidine is used as a building block for the synthesis of various pharmaceutical drugs due to its piperidine base structure, which is a common component in many medications. Its reactivity and potential biological activity make it a valuable compound in the development of new drugs.
Used in Chemical Reactions:
1-Cyclopentyl-4-aminopiperidine is used as a reactant in various chemical reactions, contributing to the synthesis of different organic compounds. Its high reactivity allows it to participate in a range of reactions, making it a versatile compound in the field of organic chemistry.
Used in Industrial Applications:
1-Cyclopentyl-4-aminopiperidine is used as a synthetic, specialty, and fine chemical in industrial applications. Its presence in these applications is due to its desirable properties, such as high reactivity, which can be harnessed for the production of various industrial products.

Check Digit Verification of cas no

The CAS Registry Mumber 132740-50-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,7,4 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 132740-50:
(8*1)+(7*3)+(6*2)+(5*7)+(4*4)+(3*0)+(2*5)+(1*0)=102
102 % 10 = 2
So 132740-50-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H20N2/c11-9-5-7-12(8-6-9)10-3-1-2-4-10/h9-10H,1-8,11H2

132740-50-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-cyclopentylpiperidin-4-amine

1.2 Other means of identification

Product number -
Other names 1-Cyclopentylpiperidin-4-amine 2HCl

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:132740-50-2 SDS

132740-50-2Relevant articles and documents

2,4-disubstituted [...] compound, and its preparation, and pharmaceutical composition and use thereof

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, (2018/02/04)

The invention discloses new 2,4-disubstituted quinazoline compounds and a preparation method, a medicinal composition and application thereof. The invention particularly relates to 2,4-disubstituted quinazoline compounds shown as a general formula I, medicinal salts thereof, precursors or derivatives thereof with the same biological function, a preparation method thereof, a composition containing one or more of the compounds, and application of the compounds in inhibiting activity of Pin1 enzyme, inhibiting activity of tumor growth and the like.

NAPHTHALENYLOXYPROPENYL DERIVATIVES HAVING INHIBITORY ACTIVITY AGAINST HISTONE DEACETYLASE AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME

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Page/Page column 80, (2008/12/05)

The present invention discloses novel naphthalenyloxypropenyl derivatives useful for inhibiting the enzyme activity of histone deacetylase, leading effective suppression of cancer cell proliferation

ALKYLCARBAMOYL NAPHTHALENYLOXY- OCTENOYLHYDROXYAMIDE DERIVATIVES HAVING INHIBITORY ACTIVITY AGAINST HISTONE DEACETYLASE AND PREPARATION THEREOF

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Page/Page column 21, (2010/11/27)

This invention discloses a novel alkylcarbamoyl naphthalenyloxy octenoylhydroxyamide derivative of formula (1) useful for inhibiting the enzyme activity of histone deacetylase, which leads to effective suppression of the cancer cell proliferation, a method for preparing same and a pharmaceutical composition comprising same.

Synthesis and structure-activity relationships of naphthamides as dopamine D3 receptor ligands

Huang,Luedtke,Freeman,Wu,Mach

, p. 1815 - 1826 (2007/10/03)

A series of naphthamides were synthesized, and the affinities of these compounds were determined for dopamine D2 and D3 receptors using radioligand binding techniques. The naphthamide compounds that were prepared include N-(1- alkylp

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