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CAS

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13632-64-9

1-(4-nitrophenyl)-1-phenyl-2-propyn-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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  • 13632-64-9 Structure

  • Basic information

    1. Product Name: 1-(4-nitrophenyl)-1-phenyl-2-propyn-1-ol
    2. Synonyms: 1-(4-nitrophenyl)-1-phenyl-2-propyn-1-ol
    3. CAS NO:13632-64-9
    4. Molecular Formula:
    5. Molecular Weight: 253.257
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 13632-64-9.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: 1-(4-nitrophenyl)-1-phenyl-2-propyn-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(4-nitrophenyl)-1-phenyl-2-propyn-1-ol(13632-64-9)
    11. EPA Substance Registry System: 1-(4-nitrophenyl)-1-phenyl-2-propyn-1-ol(13632-64-9)

  • 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: 13632-64-9(Hazardous Substances Data)

13632-64-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13632-64-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,6,3 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13632-64:
(7*1)+(6*3)+(5*6)+(4*3)+(3*2)+(2*6)+(1*4)=89
89 % 10 = 9
So 13632-64-9 is a valid CAS Registry Number.

13632-64-9Relevant articles and documents

Lewis acid catalyzed cascade reaction of 3-(2-benzenesulfonamide)propargylic alcohols to spiro[indene-benzosultam]s

Sun, Lang,Zhu, Yuanxun,Wang, Jing,Lu, Ping,Wang, Yanguang

, p. 242 - 245 (2015)

A highly efficient and convenient construction of the spiro[indene-benzosultam] skeleton from propargylic alcohols has been developed. The reaction proceeded in a Lewis acid catalyzed cascade process, including the trapping of allene carbocation with sulfonamide, electrophilic cyclization, and intramolecular Friedel-Crafts alkylation. In the presence of NIS or NBS, iodo/bromo-substituted spiro[indene-benzosultam]s could be prepared in excellent yields.

Electron-poor rhenium allenylidenes and their reactivity toward phosphines: A combined experimental and theoretical study

Coletti, Cecilia,Gonsalvi, Luca,Guerriero, Antonella,Marvelli, Lorenza,Peruzzini, Maurizio,Reginato, Gianna,Re, Nazzareno

, p. 57 - 69 (2012)

The reaction of 1-(phenyl)-1-(p-nitrophenyl)-2-propyn-1-ol with the Re(I) precursor [(triphos)(CO)2Re(OTf)] in dichloromethane at 0 °C afforded the cationic allenylidene complex [(triphos)(CO)2Re{C=C= C(C6H5)(p-

Alpha-ethynyl benzohydrols

-

, (2008/06/13)

The invention is a new process for the preparation of α-ethynyl-benzohydrols and of ring-substituted derivatives thereof by reacting the starting benzophenone or a ring-substituted derivative thereof with acetylene in a solvent delivering no protons, in t

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