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134651-05-1

4-Isoxazolamine,3,5-bis(1-methylethyl)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 134651-05-1 Structure

  • Basic information

    1. Product Name: 4-Isoxazolamine,3,5-bis(1-methylethyl)-(9CI)
    2. Synonyms: 4-Isoxazolamine,3,5-bis(1-methylethyl)-(9CI)
    3. CAS NO:134651-05-1
    4. Molecular Formula: C9H16N2O
    5. Molecular Weight: 168.23614
    6. EINECS: N/A
    7. Product Categories: OXAZOLE
    8. Mol File: 134651-05-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-Isoxazolamine,3,5-bis(1-methylethyl)-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Isoxazolamine,3,5-bis(1-methylethyl)-(9CI)(134651-05-1)
    11. EPA Substance Registry System: 4-Isoxazolamine,3,5-bis(1-methylethyl)-(9CI)(134651-05-1)

  • 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: 134651-05-1(Hazardous Substances Data)

134651-05-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134651-05-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,6,5 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 134651-05:
(8*1)+(7*3)+(6*4)+(5*6)+(4*5)+(3*1)+(2*0)+(1*5)=111
111 % 10 = 1
So 134651-05-1 is a valid CAS Registry Number.

134651-05-1Downstream Products

134651-05-1Relevant articles and documents

Transformations in the isoxazole series: Synthesis of substituted 2-aminothiazoles

Pascual, Alfons

, p. 531 - 542 (2007/10/02)

Substitued N-(isoxazol-4-yl)thioureas 1 undergo a transformation in the presence of hexacarbonylmolybdenum and acid to yield functionalized thiazoles 3 in a one-pot reaction. In a few cases, 1,4,5-trisubstituted dihydroimidazoleth, iones 4 are also isolated as side products. Mechanistic considerations are outlined and scope and limitations of this new methodology discussed.

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