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182572-80-1

N-(4-hydroxy-2-methylphenyl)-3,3-diphenylpropanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 182572-80-1 Structure

  • Basic information

    1. Product Name: N-(4-hydroxy-2-methylphenyl)-3,3-diphenylpropanamide
    2. Synonyms: N-(4-hydroxy-2-methylphenyl)-3,3-diphenylpropanamide
    3. CAS NO:182572-80-1
    4. Molecular Formula: C22H21NO2
    5. Molecular Weight: 331.40764
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 182572-80-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: N-(4-hydroxy-2-methylphenyl)-3,3-diphenylpropanamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(4-hydroxy-2-methylphenyl)-3,3-diphenylpropanamide(182572-80-1)
    11. EPA Substance Registry System: N-(4-hydroxy-2-methylphenyl)-3,3-diphenylpropanamide(182572-80-1)

  • 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: 182572-80-1(Hazardous Substances Data)

182572-80-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 182572-80-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,5,7 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 182572-80:
(8*1)+(7*8)+(6*2)+(5*5)+(4*7)+(3*2)+(2*8)+(1*0)=151
151 % 10 = 1
So 182572-80-1 is a valid CAS Registry Number.

182572-80-1Downstream Products

182572-80-1Relevant articles and documents

Lewis acid catalyzed reaction of cinnamanilides: Competition of intramolecular and intermolecular Friedel-Crafts reaction

Wang, Tai-Chi,Chen, Yeh-Long,Lee, Kuan-Han,Tzeng, Cherng-Chyi

, p. 87 - 90 (2007/10/03)

The first intermolecular Friedel-Crafts reaction of benzene leading to the formation of 3,3-diphenylpropionanilide 7 is described. 4-Methoxyaniline was reacted with cinnamoyl chloride to give 4-methoxycinnamanilide (5a), the treatment of which with aluminum (III) chloride in chlorobenzene at 120 °C or in benzene at 80 °C afforded exclusively 6-hydroxyquinolin-2(1H)-one (3a) or 4'-hydroxy-3,3-diphenylpropionanilide (7a), respectively. The formation of 7a rather than 3a in benzene indicated that an intermolecular Friedel-Crafts reaction occurred prior to the relatively more facile intramolecular ring cyclization. This intermolecular Friedel-Crafts reaction was observed during the attempted ring cyclization of cinnamanilide and its methoxy derivatives in aluminum (III) chloride/benzene. Preparation of 3a can also be achieved in 17% overall yield via the N-oxidation of 6-hydroxyquinoline followed by acetylation and hydrolysis.

An intermolecular Michael addition of benzene

Wang, Tai-Chi,Chen, Yeh-Long,Lee, Kuan-Han,Tzeng, Cherng-Chyi

, p. 6369 - 6370 (2007/10/03)

The first intermolecular Michael addition of benzene leading to the formation of 3,3-diphenylpropionanilide is described. 2-Methoxyaniline was reacted with cinnamoyl chloride to give 2-methoxycinnamanilide (1) which was treated with aluminum chloride in b

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