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1350989-93-3

2-Amino-4-ethoxycarbonylphenylboronic acid, pinacol ester is a chemical compound that features a boronic acid functional group attached to a phenyl ring, with an amino and an ethoxycarbonyl group as substituents. The pinacol ester group is also connected to the boronic acid, enhancing the compound's stability and solubility. This versatile chemical is widely utilized in organic synthesis and pharmaceutical research, serving as a fundamental building block for the creation of biologically active molecules and pharmaceuticals. Additionally, it acts as a valuable reagent in Suzuki-Miyaura cross-coupling reactions, a prevalent technique for carbon-carbon bond formation in organic chemistry.

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  • Ethyl 3-amino-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate

    Cas No: 1350989-93-3

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  • 1350989-93-3 Structure

  • Basic information

    1. Product Name: 2-AMino-4-ethoxycarbonylphenylboronic acid, pinacol ester
    2. Synonyms: 2-AMino-4-ethoxycarbonylphenylboronic acid, pinacol ester
    3. CAS NO:1350989-93-3
    4. Molecular Formula: C15H24BNO5
    5. Molecular Weight: 309.16576
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1350989-93-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 425.5±35.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.11±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 2.79±0.11(Predicted)
    10. CAS DataBase Reference: 2-AMino-4-ethoxycarbonylphenylboronic acid, pinacol ester(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-AMino-4-ethoxycarbonylphenylboronic acid, pinacol ester(1350989-93-3)
    12. EPA Substance Registry System: 2-AMino-4-ethoxycarbonylphenylboronic acid, pinacol ester(1350989-93-3)

  • 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: 1350989-93-3(Hazardous Substances Data)

1350989-93-3 Usage

Uses

Used in Organic Synthesis:
2-Amino-4-ethoxycarbonylphenylboronic acid, pinacol ester is used as a building block for the synthesis of various biologically active molecules and pharmaceuticals. Its unique structure and functional groups enable the formation of diverse chemical entities with potential applications in medicine and other fields.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-Amino-4-ethoxycarbonylphenylboronic acid, pinacol ester is employed as a key intermediate in the development of new drugs. Its presence in the molecular structure can impart specific biological activities, making it a valuable component in the design and synthesis of novel therapeutic agents.
Used in Suzuki-Miyaura Cross-Coupling Reactions:
2-Amino-4-ethoxycarbonylphenylboronic acid, pinacol ester is used as a versatile reagent in Suzuki-Miyaura cross-coupling reactions. This widely used method for carbon-carbon bond formation in organic synthesis allows for the creation of complex molecular structures with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 1350989-93-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,0,9,8 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1350989-93:
(9*1)+(8*3)+(7*5)+(6*0)+(5*9)+(4*8)+(3*9)+(2*9)+(1*3)=193
193 % 10 = 3
So 1350989-93-3 is a valid CAS Registry Number.

1350989-93-3Upstream product

1350989-93-3Downstream Products

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