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N-(2-ethyl-6-methylphenyl)benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 199107-18-1 Structure
  • Basic information

    1. Product Name: N-(2-ethyl-6-methylphenyl)benzamide
    2. Synonyms: N-(2-ethyl-6-methylphenyl)benzamide
    3. CAS NO:199107-18-1
    4. Molecular Formula: C16H17NO
    5. Molecular Weight: 239.31228
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 199107-18-1.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-(2-ethyl-6-methylphenyl)benzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(2-ethyl-6-methylphenyl)benzamide(199107-18-1)
    11. EPA Substance Registry System: N-(2-ethyl-6-methylphenyl)benzamide(199107-18-1)
  • 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: 199107-18-1(Hazardous Substances Data)

199107-18-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 199107-18-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,1,0 and 7 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 199107-18:
(8*1)+(7*9)+(6*9)+(5*1)+(4*0)+(3*7)+(2*1)+(1*8)=161
161 % 10 = 1
So 199107-18-1 is a valid CAS Registry Number.

199107-18-1Downstream Products

199107-18-1Relevant articles and documents

Copper-catalyzed selective benzylic C-O cyclization of N-o-tolylbenzamides: Synthesis of 4 H-3,1-benzoxazines

Li, Yan,Li, Zhongshu,Xiong, Tao,Zhang, Qian,Zhang, Xiangyang

supporting information; body text, p. 3522 - 3525 (2012/08/08)

A novel Selectfluor-mediated copper-catalyzed highly selective benzylic C-O cyclization for the synthesis 4H-3,1-benzoxazines is reported. The predominant selectivity for a benzylic C(sp3)-H over an aromatic C(sp 2)-H bond in N-o-tolylbenzamides is achieved.

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