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CAS

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304663-19-2

N-tert-butyl-2-(trifluoromethyl)benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 304663-19-2 Structure

  • Basic information

    1. Product Name: N-tert-butyl-2-(trifluoromethyl)benzamide
    2. Synonyms: benzamide, N-(1,1-dimethylethyl)-2-(trifluoromethyl)-; N-tert-Butyl-2-(trifluoromethyl)benzamide
    3. CAS NO:304663-19-2
    4. Molecular Formula: C12H14F3NO
    5. Molecular Weight: 245.2409
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 304663-19-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 306.5°C at 760 mmHg
    3. Flash Point: 139.1°C
    4. Appearance: N/A
    5. Density: 1.152g/cm3
    6. Vapor Pressure: 0.000771mmHg at 25°C
    7. Refractive Index: 1.463
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: N-tert-butyl-2-(trifluoromethyl)benzamide(CAS DataBase Reference)
    11. NIST Chemistry Reference: N-tert-butyl-2-(trifluoromethyl)benzamide(304663-19-2)
    12. EPA Substance Registry System: N-tert-butyl-2-(trifluoromethyl)benzamide(304663-19-2)

  • 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: 304663-19-2(Hazardous Substances Data)

304663-19-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 304663-19-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,4,6,6 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 304663-19:
(8*3)+(7*0)+(6*4)+(5*6)+(4*6)+(3*3)+(2*1)+(1*9)=122
122 % 10 = 2
So 304663-19-2 is a valid CAS Registry Number.

304663-19-2Downstream Products

304663-19-2Relevant articles and documents

Mechanochemical ritter reaction: A rapid approach to functionalized amides at room temperature

Dokli, Irena,Gredi?ak, Matija

supporting information, p. 2727 - 2732 (2015/04/27)

A fast and efficient mechanochemical Ritter reaction between alcohols and nitriles under mild conditions is demonstrated. The reaction proceeds rapidly at room temperature in a solvent-free or low-solvent environment by using a Br?nsted acid catalyst. Its general application has been verified through a substrate screening comprising a wide range of functionalized nitriles as well as secondary and tertiary alcohols. Gentle Ritter: A fast and efficient mechanochemical Ritter reaction under mild conditions is described. The reaction proceeds rapidly at room temperature in a solvent-free or low-solvent environment by using sulfuric acid as catalyst.

An efficient method for the conversion of aromatic and aliphatic nitriles to the corresponding N-tert-butyl amides: A modified Ritter reaction

Reddy, K. Laxma

, p. 1453 - 1455 (2007/10/03)

Aromatic and aliphatic nitriles react with tert-butyl acetate in the presence of a catalytic amount of sulfuric acid to give the corresponding N-tert-butyl amides in excellent yields.

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