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76670-31-0

C9H9FN2O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 76670-31-0 Structure

  • Basic information

    1. Product Name: C9H9FN2O2
    2. Synonyms:
    3. CAS NO:76670-31-0
    4. Molecular Formula:
    5. Molecular Weight: 196.181
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 76670-31-0.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: C9H9FN2O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C9H9FN2O2(76670-31-0)
    11. EPA Substance Registry System: C9H9FN2O2(76670-31-0)

  • 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: 76670-31-0(Hazardous Substances Data)

76670-31-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76670-31-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,6,7 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 76670-31:
(7*7)+(6*6)+(5*6)+(4*7)+(3*0)+(2*3)+(1*1)=150
150 % 10 = 0
So 76670-31-0 is a valid CAS Registry Number.

76670-31-0Downstream Products

76670-31-0Relevant articles and documents

Formation and Thermal Reaction of O-(N-Acetylbenzimidoyl)benzamidoxime: Comparison with the Formation of 3,5-Disubstituted 1,2,4-Oxadiazoles from O-Acetylarylamidoximes and O-Aroylacetamidoximes

Ooi, Ngan Sim,Wilson, David A.

, p. 1792 - 1799 (1980)

Salts of O-(benzimidoyl)benzamidoxime have been obtained by the action of N-chloro- or N-bromo-succinimide, or the halogens, on benzamidoxime.Acetylation of the free base gave the title compound, which underwent a thermal cyclisation, with loss of acetamide, to give 3,5-diphenyl-1,2,4-oxadiazole.The mechanism of the reaction, in diphenyl ether, closely paralleled the thermal cyclisation of O-acetylarylamidoximes and O-aroylacetamidoximes, and is thought to involve a polar cyclisation step followed by rate-determining proton transfer. 13C N.m.r. spectra for 32 oxime, amidoxime, O-acetylamidoxime, 5-methyl-1,2,4-oxadiazol-3-yl, and 3-methyl-1,2,4-oxadiazol-5-yl groups on the phenyl ring are calculated.

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