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303132-82-3

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

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  • 303132-82-3 Structure

  • Basic information

    1. Product Name: N-(4-fluorophenyl)-3,4-dimethylbenzamide
    2. Synonyms: N-(4-fluorophenyl)-3,4-dimethylbenzamide
    3. CAS NO:303132-82-3
    4. Molecular Formula: C15H14FNO
    5. Molecular Weight: 243.28
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 303132-82-3.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-fluorophenyl)-3,4-dimethylbenzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(4-fluorophenyl)-3,4-dimethylbenzamide(303132-82-3)
    11. EPA Substance Registry System: N-(4-fluorophenyl)-3,4-dimethylbenzamide(303132-82-3)

  • 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: 303132-82-3(Hazardous Substances Data)

303132-82-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 303132-82-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,3,1,3 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 303132-82:
(8*3)+(7*0)+(6*3)+(5*1)+(4*3)+(3*2)+(2*8)+(1*2)=83
83 % 10 = 3
So 303132-82-3 is a valid CAS Registry Number.

303132-82-3Relevant articles and documents

Ru(II)-Catalyzed Oxidative Olefination of Benzamides: Switchable Aza-Michael and Aza-Wacker Reaction for Synthesis of Isoindolinones

Kumar, Manoj,Verma, Akhilesh K.,Verma, Shalini

supporting information, (2020/06/25)

Selective tandem oxidative C-H olefination-aza-Michael/aza-Wacker reaction of N-arylbenzamides is achieved by fine-tuning between base and additive to access valuable 3-oxoisoindolinyls and 3-oxoisoindolinylidenes, respectively. Careful optimization and c

The influence of reaction conditions on the Diels-Alder cycloadditions of 2-thio-3-chloroacrylamides; Investigation of thermal, catalytic and microwave conditions

Kissane, Marie,Lynch, Denis,Chopra, Jay,Lawrence, Simon E.,Maguire, Anita R.

supporting information; experimental part, p. 5602 - 5613 (2011/02/18)

The Diels-Alder cycloadditions of cyclopentadiene and 2,3-dimethyl-1,3- butadiene to a range of 2-thio-3-chloroacrylamides under thermal, catalytic and microwave conditions is described. The influence of reaction conditions on the outcome of the cycloaddi

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