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92367-03-8

Benzene, iodopentanitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 92367-03-8 Structure

  • Basic information

    1. Product Name: Benzene, iodopentanitro-
    2. Synonyms:
    3. CAS NO:92367-03-8
    4. Molecular Formula: C6IN5O10
    5. Molecular Weight: 428.998
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 92367-03-8.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: Benzene, iodopentanitro-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzene, iodopentanitro-(92367-03-8)
    11. EPA Substance Registry System: Benzene, iodopentanitro-(92367-03-8)

  • 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: 92367-03-8(Hazardous Substances Data)

92367-03-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92367-03-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,3,6 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 92367-03:
(7*9)+(6*2)+(5*3)+(4*6)+(3*7)+(2*0)+(1*3)=138
138 % 10 = 8
So 92367-03-8 is a valid CAS Registry Number.

92367-03-8Upstream product

92367-03-8Downstream Products

92367-03-8Relevant articles and documents

Nitrocarbons. 4. Reaction of Polynitrobenzenes with Hydrogen Halides. Formation of Polynitrohalobenzenes

Nielsen, Arnold T.,Chafin, Andrew P.,Christian, Stephen L.

, p. 4575 - 4580 (1984)

Hexanitrobenzene and pentanitrobenzene in benzene solution react with hydrogen halides (HCl, HBr, HI, but not HF) at 25 deg C to produce high yields of pentanitrohalobenzenes and 2,3,4,6-tetranitrohalobenzenes, respectively.Pentanitrofluorobenzene also reacts readily with HCl to yield 3-chloro-2,4,5,6-tetranitrofluorobenzene, but the other pentanitrohalobenzenes are much less reactive. 1,2,3,5- and 1,2,4,5-tetranitrobenzenes react rapidly with concentrated hydrochloric or hydrobromic acids at reflux to form picryl halides and 1-halo-2,4,5-trinitrobenzenes, respectively; pentanitrotoluene reacts very slowly under these conditions to form 3-halo-2,4,5,6-tetranitrotoluenes in lower yields.The scope and limitations of this regioselective reaction are defined, and comparison is made to related reactions.A mechanism is presented and discussed.

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