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80992-30-9

3,4,5,6-tetrachloro-2-pyrrolidinocarbonylbenzoyl azide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 80992-30-9 Structure

  • Basic information

    1. Product Name: 3,4,5,6-tetrachloro-2-pyrrolidinocarbonylbenzoyl azide
    2. Synonyms:
    3. CAS NO:80992-30-9
    4. Molecular Formula:
    5. Molecular Weight: 382.033
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 80992-30-9.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: 3,4,5,6-tetrachloro-2-pyrrolidinocarbonylbenzoyl azide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,4,5,6-tetrachloro-2-pyrrolidinocarbonylbenzoyl azide(80992-30-9)
    11. EPA Substance Registry System: 3,4,5,6-tetrachloro-2-pyrrolidinocarbonylbenzoyl azide(80992-30-9)

  • 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: 80992-30-9(Hazardous Substances Data)

80992-30-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80992-30-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,9,9 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 80992-30:
(7*8)+(6*0)+(5*9)+(4*9)+(3*2)+(2*3)+(1*0)=149
149 % 10 = 9
So 80992-30-9 is a valid CAS Registry Number.

80992-30-9Relevant articles and documents

The Chemistry of Azides derived from N-substituted Phthalamic and Tetrahalogenophthalamic Acids

Au, Ting Keung,Baydar, Ahmet E.,Boyd, Gerhard V.

, p. 2884 - 2889 (2007/10/02)

Treatment of eight phthalisoimidium perchlorates with sodium azide gave N-substituted o-carbamoylbenzoyl azides (2), which yielded o-carbamoylphenyl isocyanates (4) when heated.The isocyanates derived from tertiary phthalamic acids formed 4-dialkyl ammonio-1,4-dihydro-2H-3,1-benzoxazin-2-one perchlorates (8) by the action of perchloric acid and acetic anhydride; those containing secondary amide groups cyclised to 3-alkyl-quinazoline-2,4-(1H,3H)-diones (11) at rates depending on the size of the alkyl radicals.Tetrachloro- and tetrabromo-phthalic anhydride reacted with amines to yield the corresponding amic acids, their salts, of N-substituted 3-amino-4-hydroxyphthalides.Ring-chain isomerism was also observed in the case of the azides derived from two tertiary tetrachlorophthalamic acids.

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