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146060-66-4

5-(benzyloxymethyl)-5-hexen-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 146060-66-4 Structure

  • Basic information

    1. Product Name: 5-(benzyloxymethyl)-5-hexen-2-ol
    2. Synonyms:
    3. CAS NO:146060-66-4
    4. Molecular Formula:
    5. Molecular Weight: 220.312
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 146060-66-4.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: 5-(benzyloxymethyl)-5-hexen-2-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-(benzyloxymethyl)-5-hexen-2-ol(146060-66-4)
    11. EPA Substance Registry System: 5-(benzyloxymethyl)-5-hexen-2-ol(146060-66-4)

  • 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: 146060-66-4(Hazardous Substances Data)

146060-66-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146060-66-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,0,6 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 146060-66:
(8*1)+(7*4)+(6*6)+(5*0)+(4*6)+(3*0)+(2*6)+(1*6)=114
114 % 10 = 4
So 146060-66-4 is a valid CAS Registry Number.

146060-66-4Upstream product

146060-66-4Downstream Products

146060-66-4Relevant articles and documents

Addition of 2-(chloromagnesiomethyl)-2-alkenyl ethers to epoxides followed by Pd(0)-catalyzed cyclization: A one-pot synthesis of 3-methylenetetrahydropyrans

Van Der Louw,Van Der Baan,Out,De Kanter,Bickelhaupt,Klumpp

, p. 9901 - 9916 (1992)

Addition of 2-(chloromagnesiomethyl)-2-propenyl ethers 1a and 1b to epoxides 3 affords ring opening products 6 or 7 which are converted by Pd(0) to 3-methylenetetrahydropyrans 9. Cyclization of the addition products is best effected by a catalyst system generated in situ from Pd(OAc)2 and (i-PrO)3P.

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