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Catalog Number:
40228
CAS Number:
380430-55-7
2-Amino-4-(methoxycarbonyl)phenylboronic acid hydrochloride
Purity:
≥ 98% (HPLC)
Synonym(s):
2-Amino-4-(methoxycarbonyl)benzeneboronic acid hydrochloride
Documents
$83.42 /200MG
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Product Information

2-Amino-4-(methoxycarbonyl)phenylboronic acid hydrochloride is a versatile compound widely utilized in pharmaceutical and biochemical research. This boronic acid derivative is particularly valued for its role in the development of targeted therapies and drug discovery processes. Its unique ability to form reversible covalent bonds with diols makes it an essential tool in the synthesis of complex organic molecules and in the study of biomolecular interactions. Researchers often leverage this compound in the design of protease inhibitors and in the development of novel therapeutic agents, showcasing its relevance in medicinal chemistry.

In addition to its applications in drug development, 2-Amino-4-(methoxycarbonyl)phenylboronic acid hydrochloride is also employed in various analytical techniques, including chromatography and mass spectrometry, due to its ability to enhance the detection of specific analytes. Its stability and ease of use make it a preferred choice for researchers seeking reliable results in their experiments. With its broad range of applications and significant advantages over similar compounds, this hydrochloride form stands out as a valuable asset in both academic and industrial settings.

Synonyms
2-Amino-4-(methoxycarbonyl)benzeneboronic acid hydrochloride
CAS Number
380430-55-7
Purity
≥ 98% (HPLC)
Molecular Formula
C8H10BNO4·HCl
Molecular Weight
231.44
MDL Number
MFCD02258941
PubChem ID
2737800
Melting Point
180 °C (Lit.)
Appearance
White to orange crystalline powder
Conditions
Store at RT
General Information
Synonyms
2-Amino-4-(methoxycarbonyl)benzeneboronic acid hydrochloride
CAS Number
380430-55-7
Purity
≥ 98% (HPLC)
Molecular Formula
C8H10BNO4·HCl
Molecular Weight
231.44
MDL Number
MFCD02258941
PubChem ID
2737800
Melting Point
180 °C (Lit.)
Appearance
White to orange crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-Amino-4-(methoxycarbonyl)phenylboronic acid hydrochloride is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting cancer and diabetes.
  • Bioconjugation: It is used in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other compounds, enhancing drug delivery systems.
  • Material Science: The compound is applied in the creation of advanced materials, such as sensors and catalysts, due to its unique boronic acid properties that facilitate chemical bonding.
  • Analytical Chemistry: It plays a significant role in analytical methods, particularly in the detection of sugars and other biomolecules, improving the accuracy of various assays.
  • Organic Synthesis: This chemical is a valuable reagent in organic synthesis, enabling the formation of complex molecules through cross-coupling reactions, which is essential in the development of new materials and compounds.

Citations