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193204-38-5

3-(4-benzylpiperidin-1-yl)propan-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 193204-38-5 Structure

  • Basic information

    1. Product Name: 3-(4-benzylpiperidin-1-yl)propan-1-ol
    2. Synonyms: 3-(4-benzylpiperidin-1-yl)propan-1-ol
    3. CAS NO:193204-38-5
    4. Molecular Formula:
    5. Molecular Weight: 233.354
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 193204-38-5.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: 3-(4-benzylpiperidin-1-yl)propan-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(4-benzylpiperidin-1-yl)propan-1-ol(193204-38-5)
    11. EPA Substance Registry System: 3-(4-benzylpiperidin-1-yl)propan-1-ol(193204-38-5)

  • 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: 193204-38-5(Hazardous Substances Data)

193204-38-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 193204-38-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,2,0 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 193204-38:
(8*1)+(7*9)+(6*3)+(5*2)+(4*0)+(3*4)+(2*3)+(1*8)=125
125 % 10 = 5
So 193204-38-5 is a valid CAS Registry Number.

193204-38-5Relevant articles and documents

Parallel synthesis of a series of subtype-selective NMDA receptor antagonists

Gregory, Tracy F.,Wright, Jon L.,Wise, Lawrence D.,Meltzer, Leonard T.,Serpa, Kevin A.,Konkoy, Christopher S.,Whittemore, Edward R.,Woodward, Richard M.

, p. 527 - 529 (2000)

A series of 1-(heteroarylthioalkyl)-4-benzylpiperidines was rapidly synthesized through the use of parallel synthesis to investigate the binding affinity for the NR1A/2B receptor subtype. (C) 2000 Published by Elsevier Science Ltd. All rights reserved.

Catalytic Formal Hydroamination of Allylic Alcohols Using Manganese PNP-Pincer Complexes

Duarte de Almeida, Leandro,Bourriquen, Florian,Junge, Kathrin,Beller, Matthias

, p. 4177 - 4181 (2021/03/26)

Several manganese-PNP pincer catalysts for the formal hydroamination of allylic alcohols are presented. The resulting γ-amino alcohols are selectively obtained in high yields applying Mn-1 in a tandem process under mild conditions. (Figure presented.).

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