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CAS

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1206714-49-9

1,3,5-tri-tert-butyl-6-oxocyclohexa-2,4-dienyl nitrite is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1206714-49-9 Structure

  • Basic information

    1. Product Name: 1,3,5-tri-tert-butyl-6-oxocyclohexa-2,4-dienyl nitrite
    2. Synonyms: 1,3,5-tri-tert-butyl-6-oxocyclohexa-2,4-dienyl nitrite
    3. CAS NO:1206714-49-9
    4. Molecular Formula:
    5. Molecular Weight: 307.433
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1206714-49-9.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: 1,3,5-tri-tert-butyl-6-oxocyclohexa-2,4-dienyl nitrite(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,3,5-tri-tert-butyl-6-oxocyclohexa-2,4-dienyl nitrite(1206714-49-9)
    11. EPA Substance Registry System: 1,3,5-tri-tert-butyl-6-oxocyclohexa-2,4-dienyl nitrite(1206714-49-9)

  • 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: 1206714-49-9(Hazardous Substances Data)

1206714-49-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1206714-49-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,6,7,1 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1206714-49:
(9*1)+(8*2)+(7*0)+(6*6)+(5*7)+(4*1)+(3*4)+(2*4)+(1*9)=129
129 % 10 = 9
So 1206714-49-9 is a valid CAS Registry Number.

1206714-49-9Downstream Products

1206714-49-9Relevant articles and documents

The slow rearrangement of a sterically hindered nitro-cyclohexadienone and the absence of phenol oxidation by nitrogen monoxide

Peters, Steven J.,Blood, Trisha M.,Kassabaum, Mark E.

supporting information; experimental part, p. 6104 - 6108 (2010/03/26)

The exposure of 2,4,6-tri-tert-butylphenol (1) in solution to NO 2 results in the rapid formation of 2,4,6-tri-tert-butyl-4nitro-2,5- cyclohexadienone (2), which then undergoes a slow (ca. 3 d) rearrangement in the absence of air. The mechanism, that describes this rearrangement is understood for the first time and involves the initial isomerization of 2 to form a (-ONO)-substituted cyclohexadieneone (6). The nitrite moiety undergoes bond homolysis releasing NO. while forming an oxyl radical intermediate. An lntermolecular, concerted hydrogen abstraction, which proceeds between 6 and this oxyl radical, results in the simultaneous formation of all stable products, some of which have not been previously observed, Furthermore, when 1 is exposed, to NO. under anaerobic conditions, no reaction is observed. Wiley-VCH Verlag GmbH & Co. KGaA.

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