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126502-93-0

4-(3-Benzyloxy-propyl)-3-methyl-3-phenyl-oxetan-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 126502-93-0 Structure

  • Basic information

    1. Product Name: 4-(3-Benzyloxy-propyl)-3-methyl-3-phenyl-oxetan-2-one
    2. Synonyms: 4-(3-Benzyloxy-propyl)-3-methyl-3-phenyl-oxetan-2-one
    3. CAS NO:126502-93-0
    4. Molecular Formula:
    5. Molecular Weight: 310.393
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 126502-93-0.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: 4-(3-Benzyloxy-propyl)-3-methyl-3-phenyl-oxetan-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(3-Benzyloxy-propyl)-3-methyl-3-phenyl-oxetan-2-one(126502-93-0)
    11. EPA Substance Registry System: 4-(3-Benzyloxy-propyl)-3-methyl-3-phenyl-oxetan-2-one(126502-93-0)

  • 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: 126502-93-0(Hazardous Substances Data)

126502-93-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126502-93-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,5,0 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 126502-93:
(8*1)+(7*2)+(6*6)+(5*5)+(4*0)+(3*2)+(2*9)+(1*3)=110
110 % 10 = 0
So 126502-93-0 is a valid CAS Registry Number.

126502-93-0Relevant articles and documents

Intramolecular Ring Opening Reactions of 2-Oxetanones Leading to Tetrahydrofuran Ring Formation: A Lewis Acid Study

Mead, Keith T.,Yang, Hui-Li

, p. 2991 - 2992 (2007/10/02)

A study of Lewis acid mediated intramolecular ring opening reactions of 2-oxetanones has been undertaken.Using α-substituted 4-(3-benzyloxy)propyl) analogues as substrates, we have found the reaction outcome to be highly Lewis acid dependent.

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