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1263864-82-9

2-(4-chlorobenzyl)-3-(1-naphtyl)-4-butyn-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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  • 1263864-82-9 Structure

  • Basic information

    1. Product Name: 2-(4-chlorobenzyl)-3-(1-naphtyl)-4-butyn-1-ol
    2. Synonyms: 2-(4-chlorobenzyl)-3-(1-naphtyl)-4-butyn-1-ol
    3. CAS NO:1263864-82-9
    4. Molecular Formula:
    5. Molecular Weight: 334.845
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1263864-82-9.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-(4-chlorobenzyl)-3-(1-naphtyl)-4-butyn-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(4-chlorobenzyl)-3-(1-naphtyl)-4-butyn-1-ol(1263864-82-9)
    11. EPA Substance Registry System: 2-(4-chlorobenzyl)-3-(1-naphtyl)-4-butyn-1-ol(1263864-82-9)

  • 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: 1263864-82-9(Hazardous Substances Data)

1263864-82-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1263864-82-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,3,8,6 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1263864-82:
(9*1)+(8*2)+(7*6)+(6*3)+(5*8)+(4*6)+(3*4)+(2*8)+(1*2)=179
179 % 10 = 9
So 1263864-82-9 is a valid CAS Registry Number.

1263864-82-9Upstream product

1263864-82-9Downstream Products

1263864-82-9Relevant articles and documents

Cooperative catalytic reactions using organocatalysts and transition metal catalysts: Enantioselective propargylic alkylation of propargylic esters with aldehydes

Yoshida, Akiko,Ikeda, Masahiro,Hattori, Gaku,Miyake, Yoshihiro,Nishibayashi, Yoshiaki

, p. 592 - 595 (2011)

The enantioselective propargylic alkylation of propargylic esters with aldehydes in the presence of a copper complex and an optically active secondary amine as cocatalysts has been found to give the corresponding propargylic alkylated products in good yields as a mixture of two diastereoisomers with a high enantioselectivity.

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