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[4-[benzyl(methyl)carbamoyl]phenyl]boronic acid is a chemical compound that features a boronic acid group connected to a benzene ring. This ring has a carbamoyl substituent at the para position, which includes both a benzyl and a methyl group. [4-[benzyl(methyl)carbamoyl]phenyl]boronic acid is known for its versatile applications in various fields due to its unique structure and reactivity.

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  • 1029439-41-5 Structure
  • Basic information

    1. Product Name: [4-[benzyl(methyl)carbamoyl]phenyl]boronic acid
    2. Synonyms: [4-[benzyl(methyl)carbamoyl]phenyl]boronic acid
    3. CAS NO:1029439-41-5
    4. Molecular Formula:
    5. Molecular Weight: 269.108
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1029439-41-5.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: [4-[benzyl(methyl)carbamoyl]phenyl]boronic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: [4-[benzyl(methyl)carbamoyl]phenyl]boronic acid(1029439-41-5)
    11. EPA Substance Registry System: [4-[benzyl(methyl)carbamoyl]phenyl]boronic acid(1029439-41-5)
  • 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: 1029439-41-5(Hazardous Substances Data)

1029439-41-5 Usage

Uses

Used in Organic Chemistry:
[4-[benzyl(methyl)carbamoyl]phenyl]boronic acid is used as a reagent in Suzuki-Miyaura cross-coupling reactions, which are crucial for the formation of carbon-carbon bonds. Its role as a boron source makes it a valuable component in this process.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, [4-[benzyl(methyl)carbamoyl]phenyl]boronic acid is utilized for the synthesis of various drugs. Its ability to form different chemical bonds and interact with other molecules makes it a key ingredient in creating new pharmaceutical compounds.
Used in Agrochemical Synthesis:
Similarly, [4-[benzyl(methyl)carbamoyl]phenyl]boronic acid is employed in the synthesis of agrochemicals, which are essential for the agricultural industry to protect crops and enhance their growth.
Used in Materials Science:
[4-[benzyl(methyl)carbamoyl]phenyl]boronic acid is also used in materials science for the preparation of functionalized polymers and materials. Its unique structure allows for the development of materials with specific properties tailored for various applications.
Used in Medicinal Chemistry and Drug Discovery:
Due to its potential to inhibit certain enzymes and receptors, [4-[benzyl(methyl)carbamoyl]phenyl]boronic acid has promising applications in medicinal chemistry and drug discovery. Researchers can leverage its properties to develop new drugs or improve existing ones, targeting specific biological pathways.

Check Digit Verification of cas no

The CAS Registry Mumber 1029439-41-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,9,4,3 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1029439-41:
(9*1)+(8*0)+(7*2)+(6*9)+(5*4)+(4*3)+(3*9)+(2*4)+(1*1)=145
145 % 10 = 5
So 1029439-41-5 is a valid CAS Registry Number.

1029439-41-5Downstream Products

1029439-41-5Relevant articles and documents

AMINOPYRIDINE DERIVATIVES AS PHOSPHATIDYLINOSITOL PHOSPHATE KINASE INHIBITORS

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Paragraph 0560, (2019/07/13)

The invention relates to inhibitors of PI5P4K inhibitors useful in the treatment of cancers, neurodegenerative diseases, inflammatory disorders, and metabolic diseases, having the Formula: (I) where A, B, R1, X1, X2, and W are described herein.

INHIBITORS OF FATTY ACID AMIDE HYDROLASE

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Page/Page column 209, (2008/12/05)

The present invention provide compounds, and pharmaceutical compositions thereof, encompassed by the formulae (I), (II) or (III). The present invention also provides methods for treating FAAH mediated disease, disorder or condition by administering a ther

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