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148924-04-3

3-methoxyimino-1-phenyl-1-butanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 148924-04-3 Structure

  • Basic information

    1. Product Name: 3-methoxyimino-1-phenyl-1-butanone
    2. Synonyms: 3-methoxyimino-1-phenyl-1-butanone
    3. CAS NO:148924-04-3
    4. Molecular Formula:
    5. Molecular Weight: 191.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 148924-04-3.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-methoxyimino-1-phenyl-1-butanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-methoxyimino-1-phenyl-1-butanone(148924-04-3)
    11. EPA Substance Registry System: 3-methoxyimino-1-phenyl-1-butanone(148924-04-3)

  • 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: 148924-04-3(Hazardous Substances Data)

148924-04-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 148924-04-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,9,2 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 148924-04:
(8*1)+(7*4)+(6*8)+(5*9)+(4*2)+(3*4)+(2*0)+(1*4)=153
153 % 10 = 3
So 148924-04-3 is a valid CAS Registry Number.

148924-04-3Downstream Products

148924-04-3Relevant articles and documents

N-Hydroxyamide-Containing Heterocycles. Part 2. Synthesis and Iron(III) Complex-Forming Tendency of 1-Hydroxy-2(1H)-pyrimidinone and -pyrazinone

Ohkanda, Junko,Tokumitsu, Takeshi,Mitsuhashi, Keiryo,Katoh, Akira

, p. 841 - 847 (1993)

The reaction of N-(benzyloxy)urea with 1,1,3,3-tetraethoxypropane, 4,4-dimethoxy-2-butanone, and 2,4-pentanedione under acidic conditions gave the corresponding 1-benzyloxy-2(1H)-pyrimidinones (3 and 3') in moderate yields.In contrast, the reaction of N-(

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