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81282-19-1

3-benzoyloxy-4-bromo-5-methylisoxazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 81282-19-1 Structure

  • Basic information

    1. Product Name: 3-benzoyloxy-4-bromo-5-methylisoxazole
    2. Synonyms: 3-benzoyloxy-4-bromo-5-methylisoxazole
    3. CAS NO:81282-19-1
    4. Molecular Formula:
    5. Molecular Weight: 282.093
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 81282-19-1.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: 3-benzoyloxy-4-bromo-5-methylisoxazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-benzoyloxy-4-bromo-5-methylisoxazole(81282-19-1)
    11. EPA Substance Registry System: 3-benzoyloxy-4-bromo-5-methylisoxazole(81282-19-1)

  • 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: 81282-19-1(Hazardous Substances Data)

81282-19-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81282-19-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,2,8 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 81282-19:
(7*8)+(6*1)+(5*2)+(4*8)+(3*2)+(2*1)+(1*9)=121
121 % 10 = 1
So 81282-19-1 is a valid CAS Registry Number.

81282-19-1Downstream Products

81282-19-1Relevant articles and documents

DIRECT PHENYLATION OF ISOXAZOLES USING PALLADIUM CATALYSTS. SYNTHESIS OF 4-PHENYLMUSCIMOL

Nakamura, Norio,Tajima, Yawara,Sakai, Kiyoshi

, p. 235 - 245 (2007/10/02)

Several 4-phenylisoxazoles were synthesized by the palladium-catalyzed coupling of the isoxazole ring with benzene or iodobenzene.Compound 4, thus obtained, was converted to 4-phenylmuscimol (2), according to the newly developed route to muscimol (1) from 3.

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