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CAS

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304855-07-0

2-(phenyl-hydrazono)-1-(2,4,6-trinitro-phenyl)-ethanone oxime is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 304855-07-0 Structure

  • Basic information

    1. Product Name: 2-(phenyl-hydrazono)-1-(2,4,6-trinitro-phenyl)-ethanone oxime
    2. Synonyms:
    3. CAS NO:304855-07-0
    4. Molecular Formula:
    5. Molecular Weight: 374.269
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 304855-07-0.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: 2-(phenyl-hydrazono)-1-(2,4,6-trinitro-phenyl)-ethanone oxime(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(phenyl-hydrazono)-1-(2,4,6-trinitro-phenyl)-ethanone oxime(304855-07-0)
    11. EPA Substance Registry System: 2-(phenyl-hydrazono)-1-(2,4,6-trinitro-phenyl)-ethanone oxime(304855-07-0)

  • 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: 304855-07-0(Hazardous Substances Data)

304855-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 304855-07-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,4,8,5 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 304855-07:
(8*3)+(7*0)+(6*4)+(5*8)+(4*5)+(3*5)+(2*0)+(1*7)=130
130 % 10 = 0
So 304855-07-0 is a valid CAS Registry Number.

304855-07-0Upstream product

304855-07-0Relevant articles and documents

Synthesis of 4,6-dinitro-3-R-benzo[d]isoxazoles and their transformations under the action of nucleophiles

Vinogradov,Dalinger,Starosotnikov,Shevelev

, p. 464 - 469 (2001)

A new procedure was developed for the preparation of 4,6-dinitro-3-R-benzo[d]isoxazoles (R are derivatives of the aldehyde group) based on 2,4,6-trinitrophenylacetaldehyde. The resulting compounds are characterized by the regiospecific substitution of the

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