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CAS

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17382-47-7

1-(4-Methyl-cyclohexyl)-3-phenyl-prop-2-yn-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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  • 17382-47-7 Structure

  • Basic information

    1. Product Name: 1-(4-Methyl-cyclohexyl)-3-phenyl-prop-2-yn-1-ol
    2. Synonyms: 1-(4-Methyl-cyclohexyl)-3-phenyl-prop-2-yn-1-ol
    3. CAS NO:17382-47-7
    4. Molecular Formula:
    5. Molecular Weight: 228.334
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 17382-47-7.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: 1-(4-Methyl-cyclohexyl)-3-phenyl-prop-2-yn-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(4-Methyl-cyclohexyl)-3-phenyl-prop-2-yn-1-ol(17382-47-7)
    11. EPA Substance Registry System: 1-(4-Methyl-cyclohexyl)-3-phenyl-prop-2-yn-1-ol(17382-47-7)

  • 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: 17382-47-7(Hazardous Substances Data)

17382-47-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17382-47-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,8 and 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17382-47:
(7*1)+(6*7)+(5*3)+(4*8)+(3*2)+(2*4)+(1*7)=117
117 % 10 = 7
So 17382-47-7 is a valid CAS Registry Number.

17382-47-7Upstream product

17382-47-7Downstream Products

17382-47-7Relevant articles and documents

Ru(ii)-catalyzed allenylation and sequential annulation of: N -tosylbenzamides with propargyl alcohols

Kumar, Shreemoyee,Nair, Akshay M.,Volla, Chandra M. R.

, p. 6280 - 6283 (2021)

We hereby report Ru(ii)-catalyzed C(sp2)-H allenylation of N-tosylbenzamides to access multi-substituted allenylamides. Furthermore, the allenylamides were converted to the corresponding isoquinolone derivatives via base mediated annulation. The current protocol features low catalyst loading, mild reaction conditions, high functional group compatibility and desired scalability. The unique functionality of the afforded allenes allowed further transformations to expand the practicality of the protocol. This journal is

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