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473259-27-7

2-pentyl-1-phenylpiperidine-2-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 473259-27-7 Structure

  • Basic information

    1. Product Name: 2-pentyl-1-phenylpiperidine-2-carbonitrile
    2. Synonyms: 2-pentyl-1-phenylpiperidine-2-carbonitrile
    3. CAS NO:473259-27-7
    4. Molecular Formula:
    5. Molecular Weight: 256.391
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 473259-27-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-pentyl-1-phenylpiperidine-2-carbonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-pentyl-1-phenylpiperidine-2-carbonitrile(473259-27-7)
    11. EPA Substance Registry System: 2-pentyl-1-phenylpiperidine-2-carbonitrile(473259-27-7)

  • 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: 473259-27-7(Hazardous Substances Data)

473259-27-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 473259-27-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,3,2,5 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 473259-27:
(8*4)+(7*7)+(6*3)+(5*2)+(4*5)+(3*9)+(2*2)+(1*7)=167
167 % 10 = 7
So 473259-27-7 is a valid CAS Registry Number.

473259-27-7Downstream Products

473259-27-7Relevant articles and documents

Synthesis of α-CN and α-CF3 N-heterocycles through tandem nucleophilic additions

Han, Junbin,Xu, Bo,Hammond, Gerald B.

, p. 3450 - 3453 (2011/08/07)

Using a readily available secondary aminoalkyne as starting material, a powerful strategy was discovered to prepare precursors of biologically important unnatural cyclic aminoacids and fluorinated N-heterocycles with important ring sizes (e.g., 5-7) in a

Synthesis of 1-Azaspiroundecane ring system via Thorpe-Ziegler annulation of 2-Cyano-2-(4-Cyano-Tethered) Arylpiperidines

Malassene, Richard,Toupet, Loic,Hurvois, Jean-Pierre,Moinet, Claude

, p. 895 - 898 (2007/10/03)

An efficient stereocontrolled route to the spiro[5.5]undecan framework of the histrionicotoxin alkaloids, employing anodic cyanation and Thorpe-Ziegler cyclization as key steps, is described. In the process of gaining information concerning the hydrolysis of the cyanoenamine function in 8, an unexpected intramolecular Friedel-Crafts type reaction provided the aza-fluorene 10.

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