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CAS

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100378-99-2

(5-dihydroxyboranyl-2-methyl-phenyl)-urea, also known as boronic acid-functionalized phenyl-urea, is a chemical compound that features both boronic acid and urea functional groups. This unique combination endows the compound with versatile properties, making it a valuable asset in various fields such as organic chemistry, medicinal chemistry, materials science, and catalysis. The boronic acid group forms reversible covalent bonds with diols, while the urea group contributes to hydrogen bonding interactions, solubility, and reactivity.

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  • 100378-99-2 Structure

  • Basic information

    1. Product Name: (5-dihydroxyboranyl-2-methyl-phenyl)-urea
    2. Synonyms:
    3. CAS NO:100378-99-2
    4. Molecular Formula:
    5. Molecular Weight: 193.998
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 100378-99-2.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: (5-dihydroxyboranyl-2-methyl-phenyl)-urea(CAS DataBase Reference)
    10. NIST Chemistry Reference: (5-dihydroxyboranyl-2-methyl-phenyl)-urea(100378-99-2)
    11. EPA Substance Registry System: (5-dihydroxyboranyl-2-methyl-phenyl)-urea(100378-99-2)

  • 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: 100378-99-2(Hazardous Substances Data)

100378-99-2 Usage

Uses

Used in Organic Chemistry:
(5-dihydroxyboranyl-2-methyl-phenyl)-urea is used as a synthetic building block for the creation of new organic compounds. Its ability to form reversible covalent bonds with diols makes it a valuable tool in the synthesis of complex molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (5-dihydroxyboranyl-2-methyl-phenyl)-urea is used as a molecular scaffold for the development of novel drug molecules. (5-dihydroxyboranyl-2-methyl-phenyl)-urea's unique functional groups can be exploited to design drugs with specific targeting and binding properties.
Used in Materials Science:
(5-dihydroxyboranyl-2-methyl-phenyl)-urea is utilized as a component in the development of new materials with tailored properties. (5-dihydroxyboranyl-2-methyl-phenyl)-urea's functional groups can influence the material's reactivity, solubility, and interaction with other molecules, making it a promising candidate for creating advanced materials.
Used in Catalysis:
As a catalyst or catalyst precursor, (5-dihydroxyboranyl-2-methyl-phenyl)-urea is used in various chemical reactions to enhance reaction rates and selectivity. (5-dihydroxyboranyl-2-methyl-phenyl)-urea's functional groups can facilitate specific reaction pathways, making it a valuable asset in the field of catalysis.

Check Digit Verification of cas no

The CAS Registry Mumber 100378-99-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,3,7 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 100378-99:
(8*1)+(7*0)+(6*0)+(5*3)+(4*7)+(3*8)+(2*9)+(1*9)=102
102 % 10 = 2
So 100378-99-2 is a valid CAS Registry Number.

100378-99-2Upstream product

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