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CAS

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54606-03-0

trans-(4-methyl-3-phenyl-4,5-dihydroisoxazol-5-yl)(phenyl)methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 54606-03-0 Structure

  • Basic information

    1. Product Name: trans-(4-methyl-3-phenyl-4,5-dihydroisoxazol-5-yl)(phenyl)methanone
    2. Synonyms:
    3. CAS NO:54606-03-0
    4. Molecular Formula:
    5. Molecular Weight: 265.312
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 54606-03-0.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: trans-(4-methyl-3-phenyl-4,5-dihydroisoxazol-5-yl)(phenyl)methanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: trans-(4-methyl-3-phenyl-4,5-dihydroisoxazol-5-yl)(phenyl)methanone(54606-03-0)
    11. EPA Substance Registry System: trans-(4-methyl-3-phenyl-4,5-dihydroisoxazol-5-yl)(phenyl)methanone(54606-03-0)

  • 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: 54606-03-0(Hazardous Substances Data)

54606-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54606-03-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,6,0 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 54606-03:
(7*5)+(6*4)+(5*6)+(4*0)+(3*6)+(2*0)+(1*3)=110
110 % 10 = 0
So 54606-03-0 is a valid CAS Registry Number.

54606-03-0Downstream Products

54606-03-0Relevant articles and documents

Synthesis of Isoxazolines from Nitroalkanes via a [4+1]-Annulation Strategy

Ushakov, Pavel Yu.,Khatuntseva, Elizaveta A.,Nelyubina, Yulia V.,Tabolin, Andrey A.,Ioffe, Sema L.,Sukhorukov, Alexey Yu.

, p. 5322 - 5327 (2019)

A novel access to isoxazolines was developed using the [4+1]-annulation of α-keto-stabilized sulfur ylides with N,N-bis(siloxy)enamines derived from aliphatic nitro compounds. The resulting 5-keto-substituted isoxazolines were shown to be convenient precursors of polysubstituted 3-hydroxypyrrolidines via the one-pot catalytic N?O hydrogenolysis/intramolecular reductive amination sequence. Application of this approach to the formal synthesis of Merck's potent NK1 receptor antagonist was demonstrated. (Figure presented.).

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