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97130-11-5

5,5-dimethyl-3,6-diphenyl-6-pyrrolidino-5,6-dihydro-2-pyranone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 97130-11-5 Structure

  • Basic information

    1. Product Name: 5,5-dimethyl-3,6-diphenyl-6-pyrrolidino-5,6-dihydro-2-pyranone
    2. Synonyms: 5,5-dimethyl-3,6-diphenyl-6-pyrrolidino-5,6-dihydro-2-pyranone
    3. CAS NO:97130-11-5
    4. Molecular Formula:
    5. Molecular Weight: 347.457
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 97130-11-5.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: 5,5-dimethyl-3,6-diphenyl-6-pyrrolidino-5,6-dihydro-2-pyranone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5,5-dimethyl-3,6-diphenyl-6-pyrrolidino-5,6-dihydro-2-pyranone(97130-11-5)
    11. EPA Substance Registry System: 5,5-dimethyl-3,6-diphenyl-6-pyrrolidino-5,6-dihydro-2-pyranone(97130-11-5)

  • 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: 97130-11-5(Hazardous Substances Data)

97130-11-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97130-11-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,1,3 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 97130-11:
(7*9)+(6*7)+(5*1)+(4*3)+(3*0)+(2*1)+(1*1)=125
125 % 10 = 5
So 97130-11-5 is a valid CAS Registry Number.

97130-11-5Relevant articles and documents

Diels-alder cycloadditions of 1,3,4,-oxadiazin-6-ones with electron rich pi systems

Padwa, Albert,Eisenbarth, Philipp

, p. 283 - 296 (2007/10/02)

A study of the cycloaddition behavior of several 2,5-disubstituted 1,3,4-oxadiazin-6-ones with electron rich pi bonds has been carried out. trans-1-Propenylpyrrolidine was found to react with the oxadiazinone ring system to give rise to a ring opened diazatrienyl substituted carboxylic acid. Further heating of the acid results in decarboxylation, hydrolysis, cyclization and pyrrolidine elimination to produce a disubstituted pyrazole. Reaction with the trisubstituted enamine 1 - ( 2 - methyl-propenyl) pyrrolidine, was also studied in some detail. The cycloadditions encountered can be rationalized as proceeding by an initial Diels-Alder reaction followed by cheletropic extrusion of nitrogen to produce a ketoketene intermediate. The fate of the ketene is markedly dependent upon the overall pattern of substitution. Some of the products formed can be explained in terms of a competitive migration of the pyrrolidino group to the ketene and benzoyl groups. With one system the major cycloadduct is derived from the Diels-Alder reaction of a transient azaketene tautomer formed by an electrocyclic opening of the oxadiazinone ring.

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