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CAS

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54788-42-0

2-bromotyrosine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 54788-42-0 Structure

  • Basic information

    1. Product Name: 2-bromotyrosine
    2. Synonyms:
    3. CAS NO:54788-42-0
    4. Molecular Formula: C9H10BrNO3
    5. Molecular Weight: 260.0846
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 54788-42-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 430°C at 760 mmHg
    3. Flash Point: 213.9°C
    4. Appearance: N/A
    5. Density: 1.71g/cm3
    6. Vapor Pressure: 3.7E-08mmHg at 25°C
    7. Refractive Index: 1.644
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-bromotyrosine(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-bromotyrosine(54788-42-0)
    12. EPA Substance Registry System: 2-bromotyrosine(54788-42-0)

  • 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: 54788-42-0(Hazardous Substances Data)

54788-42-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54788-42-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,7,8 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 54788-42:
(7*5)+(6*4)+(5*7)+(4*8)+(3*8)+(2*4)+(1*2)=160
160 % 10 = 0
So 54788-42-0 is a valid CAS Registry Number.

54788-42-0Downstream Products

54788-42-0Relevant articles and documents

Synthesis and microbiological activities of some monohalogenated analogs of tyrosine

McCord,Smith,Winters,Grimes,Hulme,Robinson,Gage,Davis

, p. 26 - 29 (2007/10/06)

2 Chlorotyrosine and 2 bromotyrosine, as well as the previously reported 2 fluorotyrosine, were synthesized by hydrolysis of the condensation products from the appropriate benzyl bromide and ethyl acetamidomalonate and were compared with the corresponding

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