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1-[4-(PIPERIDIN-1-YLCARBONYL)PHENYL]METHANAMINE, a piperidine derivative, is a crystalline solid with a molecular formula of C14H19N3O and a molecular weight of 245.32 g/mol. It features a piperidine ring, a carbonyl group, and a phenyl group, which are significant structural motifs in many biologically active molecules. Its chemical properties and reactivity make it a valuable building block for the synthesis of various bioactive compounds, particularly in medicinal chemistry and drug development.

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  • 292635-34-8 Structure
  • Basic information

    1. Product Name: 1-[4-(PIPERIDIN-1-YLCARBONYL)PHENYL]METHANAMINE
    2. Synonyms: 1-[4-(AMINOMETHYL)BENZOYL]-PIPERIDINE;1-[4-(PIPERIDIN-1-YLCARBONYL)PHENYL]METHANAMINE;1-[4-(1-piperidinylcarbonyl)phenyl]methanamine(SALTDATA: HCl);[4-(Piperidin-1-ylcarbonyl)benzyl]amine;[4-(aminomethyl)phenyl]-(1-piperidyl)methanone;[4-(aminomethyl)phenyl]-piperidin-1-ylmethanone;[4-(aminomethyl)phenyl]-piperidin-1-yl-methanone;[4-(aminomethyl)phenyl]-piperidino-methanone
    3. CAS NO:292635-34-8
    4. Molecular Formula: C13H18N2O
    5. Molecular Weight: 218.298
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 292635-34-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 397.6±25.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.122±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 8.87±0.10(Predicted)
    10. CAS DataBase Reference: 1-[4-(PIPERIDIN-1-YLCARBONYL)PHENYL]METHANAMINE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-[4-(PIPERIDIN-1-YLCARBONYL)PHENYL]METHANAMINE(292635-34-8)
    12. EPA Substance Registry System: 1-[4-(PIPERIDIN-1-YLCARBONYL)PHENYL]METHANAMINE(292635-34-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 292635-34-8(Hazardous Substances Data)

292635-34-8 Usage

Uses

Used in Medicinal Chemistry:
1-[4-(PIPERIDIN-1-YLCARBONYL)PHENYL]METHANAMINE is used as a building block for the synthesis of bioactive compounds due to its structural features and reactivity.
Used in Drug Development:
1-[4-(PIPERIDIN-1-YLCARBONYL)PHENYL]METHANAMINE is used as a precursor in the development of new pharmaceuticals for its potential to contribute to the creation of molecules with therapeutic properties.
While the provided materials do not specify particular applications or industries for 1-[4-(PIPERIDIN-1-YLCARBONYL)PHENYL]METHANAMINE, its use in medicinal chemistry and drug development is a broad application that can encompass various therapeutic areas and industries within the pharmaceutical sector. Further research and development would be necessary to identify specific uses in different medical fields or industries.

Check Digit Verification of cas no

The CAS Registry Mumber 292635-34-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,2,6,3 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 292635-34:
(8*2)+(7*9)+(6*2)+(5*6)+(4*3)+(3*5)+(2*3)+(1*4)=158
158 % 10 = 8
So 292635-34-8 is a valid CAS Registry Number.

292635-34-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-(aminomethyl)phenyl]-piperidin-1-ylmethanone

1.2 Other means of identification

Product number -
Other names 1-[4-(piperidin-1-ylcarbonyl)phenyl]methanamine

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:292635-34-8 SDS

292635-34-8Downstream Products

292635-34-8Relevant articles and documents

Improved syntheses of 5′- S -(2-Aminoethyl)-6- N -(4-nitrobenzyl)- 5′-thioadenosine (SAENTA), analogues, and fluorescent probe conjugates: Analysis of cell-surface human equilibrative nucleoside transporter 1 (hENT1) levels for prediction of the antitumor

Robins, Morris J.,Peng, Yunshan,Damaraju, Vijaya L.,Mowles, Delores,Barron, Geraldine,Tackaberry, Tracey,Young, James D.,Cass, Carol E.

experimental part, p. 6040 - 6053 (2010/11/02)

5′-S-(2-Aminoethyl)-6-N-(4-nitrobenzyl)-5′-thioadenosine (SAENTA), 5′-S-(2-acetamidoethyl)-6-N-[(4-substituted)benzyl]-5′- thioadenosine analogues, 5′-S-[2-(6-aminohexanamido)]ethyl-6-N-(4- nitrobenzyl)-5′-thioadenosine (SAHENTA), and related compounds we

Aminomethylation of functionalized organozinc reagents and grignard reagents using immonium trifluoroacetates

Millot, Nicolas,Piazza, Claudia,Avolio, Salvatore,Knochel, Paul

, p. 941 - 948 (2007/10/03)

New immonium trifluoroacetates 1 and 2 react readily with functionalized organozinc or magnesium reagents leading to the corresponding aminomethylated products of type 5 and 7. The resulting bis-allylamines were deallylated leading to primary amines.

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