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Ethanone, 1-(3a,5,6,6a-tetrahydro-4H-cyclopent[d]isoxazol-3-yl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • Ethanone, 1-(3a,5,6,6a-tetrahydro-4H-cyclopent[d]isoxazol-3-yl)- (9CI)

    Cas No: 674804-66-1

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  • 674804-66-1 Structure
  • Basic information

    1. Product Name: Ethanone, 1-(3a,5,6,6a-tetrahydro-4H-cyclopent[d]isoxazol-3-yl)- (9CI)
    2. Synonyms: Ethanone, 1-(3a,5,6,6a-tetrahydro-4H-cyclopent[d]isoxazol-3-yl)- (9CI)
    3. CAS NO:674804-66-1
    4. Molecular Formula: C8H11NO2
    5. Molecular Weight: 153.17844
    6. EINECS: N/A
    7. Product Categories: CYCLOPENTANE;ACETYLGROUP
    8. Mol File: 674804-66-1.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: Ethanone, 1-(3a,5,6,6a-tetrahydro-4H-cyclopent[d]isoxazol-3-yl)- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ethanone, 1-(3a,5,6,6a-tetrahydro-4H-cyclopent[d]isoxazol-3-yl)- (9CI)(674804-66-1)
    11. EPA Substance Registry System: Ethanone, 1-(3a,5,6,6a-tetrahydro-4H-cyclopent[d]isoxazol-3-yl)- (9CI)(674804-66-1)
  • 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: 674804-66-1(Hazardous Substances Data)

674804-66-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 674804-66-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,4,8,0 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 674804-66:
(8*6)+(7*7)+(6*4)+(5*8)+(4*0)+(3*4)+(2*6)+(1*6)=191
191 % 10 = 1
So 674804-66-1 is a valid CAS Registry Number.

674804-66-1Downstream Products

674804-66-1Relevant articles and documents

A convenient and efficient one-pot synthesis of 3-acylisoxazoles using iron(III) salts

Itoh, Ken-Ichi,Sakamaki, Hiroshi,Nakazato, Noriko,Horiuchi, Atsuo,Horn, Ernst,Horiuchi, C. Akira

, p. 3541 - 3548 (2007/10/03)

3-Acylisoxazoles were synthesized by the reaction of alkenes or alkynes with ketones (acetone or acetophenone), as both a reagent and the solvent, by three methods: iron(III) nitrate under reflux, iron(III) salt-nitrogen dioxide (NO2) at room temperature,

Formation of isoxazole derivatives via nitrile oxide using ammonium cerium nitrate (CAN): A novel one-pot synthesis of 3-acetyl- and 3-benzoylisoxazole derivatives

Itoh, Ken-Ichi,Horiuchi, C. Akira

, p. 1671 - 1681 (2007/10/03)

The reactions of alkenes and alkynes with ammonium cerium(IV) nitrate ((NH4)2Ce(NO3)6, CAN(IV)) in acetone under reflux gave the corresponding 3-acetyl-4,5-dihydroisoxazole and 3-acetylisoxazole derivatives. In the case of acetophenone, 3-benzoyl-4,5- dihydroisoxazole and 3-benzoylisoxazole derivatives were obtained. Reaction of acetone with CAN(IV) afforded the corresponding furoxan (3,4-diacetyl-1,2,5- oxadiazole 2-oxide) as the dimer of nitrile oxide. Moreover, it was found that yields of isoxazole derivatives were improved using ammonium cerium(III) nitrate tetrahydrate ((NH4)2Ce(NO3) 5·4H2O, CAN(III))-formic acid. The reaction mechanisms based on nitration and formation of nitrile oxide mediated by CAN(IV) or CAN(III) from acetone or acetophenone are also proposed.

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