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CAS

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132353-08-3

3-phenyl-2-propynyl 2-diazo-3-oxobutanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 132353-08-3 Structure

  • Basic information

    1. Product Name: 3-phenyl-2-propynyl 2-diazo-3-oxobutanoate
    2. Synonyms: 3-phenyl-2-propynyl 2-diazo-3-oxobutanoate
    3. CAS NO:132353-08-3
    4. Molecular Formula:
    5. Molecular Weight: 242.234
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 132353-08-3.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: 3-phenyl-2-propynyl 2-diazo-3-oxobutanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-phenyl-2-propynyl 2-diazo-3-oxobutanoate(132353-08-3)
    11. EPA Substance Registry System: 3-phenyl-2-propynyl 2-diazo-3-oxobutanoate(132353-08-3)

  • 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: 132353-08-3(Hazardous Substances Data)

132353-08-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132353-08-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,3,5 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 132353-08:
(8*1)+(7*3)+(6*2)+(5*3)+(4*5)+(3*3)+(2*0)+(1*8)=93
93 % 10 = 3
So 132353-08-3 is a valid CAS Registry Number.

132353-08-3Relevant articles and documents

Preparation of oxygenated heterocycles via the cyclization reaction of α-diazo substituted alkynes

Kinder,Padwa

, p. 6835 - 6838 (1990)

treatment of a series of α-diazo alkynyl substituted ketones with rhodium (II) carboxylates results in the formation of vinyl rhodium carbenoids. These species undergo further cyclization onto a neighboring carbonyl group to produce furans.

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