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4-acetyl-N-(2-chlorophenyl)benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 904078-10-0 Structure
  • Basic information

    1. Product Name: 4-acetyl-N-(2-chlorophenyl)benzamide
    2. Synonyms: 4-acetyl-N-(2-chlorophenyl)benzamide
    3. CAS NO:904078-10-0
    4. Molecular Formula:
    5. Molecular Weight: 273.719
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 904078-10-0.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: 4-acetyl-N-(2-chlorophenyl)benzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-acetyl-N-(2-chlorophenyl)benzamide(904078-10-0)
    11. EPA Substance Registry System: 4-acetyl-N-(2-chlorophenyl)benzamide(904078-10-0)
  • 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: 904078-10-0(Hazardous Substances Data)

904078-10-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 904078-10-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,4,0,7 and 8 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 904078-10:
(8*9)+(7*0)+(6*4)+(5*0)+(4*7)+(3*8)+(2*1)+(1*0)=150
150 % 10 = 0
So 904078-10-0 is a valid CAS Registry Number.

904078-10-0Downstream Products

904078-10-0Relevant articles and documents

Pd(OAc)2-catalyzed carbonylative coupling of aryl iodide with ortho-haloamines in water

Tambade, Pawan J.,Patil, Yogesh P.,Qureshi, Ziyauddin S.,Dhake, Kishor P.,Bhanage, Bhalchandra M.

, p. 176 - 185 (2012)

The carbonylative cross coupling of aryl iodide with ortho-haloaniline to ortho-haloanilide using phosphine-free Pd(OAc)2 catalyst in water as a reaction medium has been studied. The present protocol facilitated the reaction of o-haloanilines with a wide variety of hindered and functionalized aryl iodides, affording good yields of the desired products. The protocol was also extended for the synthesis of benzoxazoles through cyclization of ortho-haloanilide using Cu(acac)2 catalyst. Taylor & Francis Group, LLC.

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