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854001-04-0

(Z)-1-Phenyl-dec-4-en-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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  • 854001-04-0 Structure

  • Basic information

    1. Product Name: (Z)-1-Phenyl-dec-4-en-1-ol
    2. Synonyms: (Z)-1-Phenyl-dec-4-en-1-ol
    3. CAS NO:854001-04-0
    4. Molecular Formula:
    5. Molecular Weight: 232.366
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 854001-04-0.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: (Z)-1-Phenyl-dec-4-en-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (Z)-1-Phenyl-dec-4-en-1-ol(854001-04-0)
    11. EPA Substance Registry System: (Z)-1-Phenyl-dec-4-en-1-ol(854001-04-0)

  • 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: 854001-04-0(Hazardous Substances Data)

854001-04-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 854001-04-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,4,0,0 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 854001-04:
(8*8)+(7*5)+(6*4)+(5*0)+(4*0)+(3*1)+(2*0)+(1*4)=130
130 % 10 = 0
So 854001-04-0 is a valid CAS Registry Number.

854001-04-0Relevant articles and documents

One-pot regio- and stereoselective cyclization of 1,2,n-triols

Zheng, Tao,Narayan, Radha S.,Schomaker, Jennifer M.,Borhan, Babak

, p. 6946 - 6947 (2005)

A simple and efficient process to cyclize triols containing a 1,2-diol functionality with a pendant hydroxyl group is presented. The one-pot procedure converts the 1,2-diol into an ortho ester in situ, which upon treatment with a Lewis acid generates a cyclic acetoxonium intermediate. This intermediate is subsequently trapped by the pendant hydroxyl group to generate a cyclic ether. The stereochemistry of the 1,2-diol is transferred to the product with complete fidelity (inversion at the site of cyclization), and the reaction proceeds with high regioselectivity. The process is akin to the Lewis acid-catalyzed intramolecular ring-opening of epoxides with hydroxyl groups yielding cyclic ethers of various sizes with regio- and stereochemical control. Copyright

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