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96784-44-0

3-Carbamoyl-4,5,5-tris(4-methoxyphenyl)-1H-pyrrol-2(5H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 96784-44-0 Structure

  • Basic information

    1. Product Name: 3-Carbamoyl-4,5,5-tris(4-methoxyphenyl)-1H-pyrrol-2(5H)-one
    2. Synonyms: 3-Carbamoyl-4,5,5-tris(4-methoxyphenyl)-1H-pyrrol-2(5H)-one
    3. CAS NO:96784-44-0
    4. Molecular Formula:
    5. Molecular Weight: 444.487
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 96784-44-0.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: 3-Carbamoyl-4,5,5-tris(4-methoxyphenyl)-1H-pyrrol-2(5H)-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-Carbamoyl-4,5,5-tris(4-methoxyphenyl)-1H-pyrrol-2(5H)-one(96784-44-0)
    11. EPA Substance Registry System: 3-Carbamoyl-4,5,5-tris(4-methoxyphenyl)-1H-pyrrol-2(5H)-one(96784-44-0)

  • 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: 96784-44-0(Hazardous Substances Data)

96784-44-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96784-44-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,7,8 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 96784-44:
(7*9)+(6*6)+(5*7)+(4*8)+(3*4)+(2*4)+(1*4)=190
190 % 10 = 0
So 96784-44-0 is a valid CAS Registry Number.

96784-44-0Downstream Products

96784-44-0Relevant articles and documents

Reaction of Olefins with Malonamide in the Presence of Manganese(III) Acetate. Formation of α,β-Unsaturated γ-Lactones and γ-Lactams

Nishino, Hiroshi

, p. 217 - 222 (1985)

The reaction of olefins with malonamide in the presence of manganese(III) acetate gave 2-buten-4-olides and/or 1H-pyrrol-2(5H)-ones in one-step, short reaction time and moderate yields.The product distribution can be accounted for in terms of the stabilization of the intermediate carbocation in the oxidation process.The synthetic application and limitation, and the oxidation mechanism for the formations of α,β-unsaturated γ-lactones and γ-lactams are discussed.

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