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CAS

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22724-22-7

5-bromo-6-hydroxymethyluracil is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 22724-22-7 Structure

  • Basic information

    1. Product Name: 5-bromo-6-hydroxymethyluracil
    2. Synonyms:
    3. CAS NO:22724-22-7
    4. Molecular Formula:
    5. Molecular Weight: 221.01
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 22724-22-7.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: 5-bromo-6-hydroxymethyluracil(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-bromo-6-hydroxymethyluracil(22724-22-7)
    11. EPA Substance Registry System: 5-bromo-6-hydroxymethyluracil(22724-22-7)

  • 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: 22724-22-7(Hazardous Substances Data)

22724-22-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22724-22-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,7,2 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 22724-22:
(7*2)+(6*2)+(5*7)+(4*2)+(3*4)+(2*2)+(1*2)=87
87 % 10 = 7
So 22724-22-7 is a valid CAS Registry Number.

22724-22-7Upstream product

22724-22-7Downstream Products

22724-22-7Relevant articles and documents

Reaction of Halogenated Uracils with KI

Chernikova,Spirikhin,Abdullin,Yunusov

, p. 1140 - 1143 (2017)

Treatment of 5-iodo-1,3,6-trimethyluracil or 5-bromo-1,3,6-trimethyluracil with H2SO4 (5%) in the presence of an excess of KI at 80°C for 5 h produced 1,3,6-trimethyluracil as the only product. Analogous treatment of N-bromo-6-iodomethyluracil gave a mixture with 5-bromo-6-iodomethyluracil as the main constituent. The reaction with an excess of KI in MeOH at 50°C formed 5-bromo-6-hydroxymethyluracil, N(1)-iodo-5-bromo-6-hydroxymethyluracil, N(3)-iodo-5-bromo-6-iodomethyluracil, and 5-bromo-6-iodomethyluracil depending on the reaction time.

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