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N-(4-Bromo-phenyl)-2-hydroxy-2-(4-nitro-phenyl)-acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 92885-00-2 Structure
  • Basic information

    1. Product Name: N-(4-Bromo-phenyl)-2-hydroxy-2-(4-nitro-phenyl)-acetamide
    2. Synonyms:
    3. CAS NO:92885-00-2
    4. Molecular Formula:
    5. Molecular Weight: 351.156
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 92885-00-2.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: N-(4-Bromo-phenyl)-2-hydroxy-2-(4-nitro-phenyl)-acetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(4-Bromo-phenyl)-2-hydroxy-2-(4-nitro-phenyl)-acetamide(92885-00-2)
    11. EPA Substance Registry System: N-(4-Bromo-phenyl)-2-hydroxy-2-(4-nitro-phenyl)-acetamide(92885-00-2)
  • 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: 92885-00-2(Hazardous Substances Data)

92885-00-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92885-00-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,8,8 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 92885-00:
(7*9)+(6*2)+(5*8)+(4*8)+(3*5)+(2*0)+(1*0)=162
162 % 10 = 2
So 92885-00-2 is a valid CAS Registry Number.

92885-00-2Downstream Products

92885-00-2Relevant articles and documents

1,3-DIARYL-2,2-DIHALOAZIRIDINES IN NITRATION AND BROMINATION REACTIONS

Khlebnikov, A. F.,Kostikov, R. R.

, p. 739 - 744 (1984)

In the nitration of 3-(4-nitrophenyl)-1-phenyl-2,2-dichloroaziridine in acetic acid, 1-(o- and p-nitrophenyl)-derivatives are formed in a 35:65 ratio. 1,3-Diphenyl-2,2-dichloroaziridine undergoes opening of the three-membered ring under the same conditions, forming a mixture of o- and p-nitroanilides and 2-nitro-4-chloroanilides of 2-acetoxy (or 2-chloro)-2-phenylacetic acids.The bromination of 3-(4-nitrophenyl)-1-phenyl-2,2-dichloroaziridine in aqueous acetic acid leads to 1-(4-bromophenyl)-3-(4-nitrophenyl)-2,2-dichloroaziridine, while in a mixture of acetic acid and acetic anhydride it leads to the anilide of 2-bromo-2-phenylacetic acid and 2-bromo-N-(2,4-dibromophenyl)-1-(4-nitrophenyl)-2,2-dichloroethylamine.

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