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5-(2,4,6-Trimethyl-phenyl)-tetrahydro-furan-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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  • 103624-23-3 Structure
  • Basic information

    1. Product Name: 5-(2,4,6-Trimethyl-phenyl)-tetrahydro-furan-2-ol
    2. Synonyms:
    3. CAS NO:103624-23-3
    4. Molecular Formula:
    5. Molecular Weight: 206.285
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 103624-23-3.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-(2,4,6-Trimethyl-phenyl)-tetrahydro-furan-2-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-(2,4,6-Trimethyl-phenyl)-tetrahydro-furan-2-ol(103624-23-3)
    11. EPA Substance Registry System: 5-(2,4,6-Trimethyl-phenyl)-tetrahydro-furan-2-ol(103624-23-3)
  • 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: 103624-23-3(Hazardous Substances Data)

103624-23-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103624-23-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,6,2 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 103624-23:
(8*1)+(7*0)+(6*3)+(5*6)+(4*2)+(3*4)+(2*2)+(1*3)=83
83 % 10 = 3
So 103624-23-3 is a valid CAS Registry Number.

103624-23-3Downstream Products

103624-23-3Relevant articles and documents

SYNTHESE DE COMPOSES DIHYDRO-2,3 FURANNIQUES PAR HYDROBORATION D'ALCOOLS β-ACETYLENIQUES

Dana, Gilbert,Figadere, Bruno,Touboul, Estera

, p. 5683 - 5684 (1985)

Hydroboration of β acetylenic alcohols followed by NaOH/H2O2 oxidation leads to hemiacetals of γ aldols which are easily dehydrated to 2,3-dihydrofuran compounds.The reaction gives good yields with hindered alcohols and its stereochemistry may be controlled during the organometallic synthesis of the starting alcohol.

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