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Catalog Number:
40119
CAS Number:
1256355-23-3
Chlorhydrate d'acide 3-(diméthylamino)phénylboronique
Purity:
98 - 105 % (dosage par titrage)
Synonym(s):
Chlorhydrate d'acide 3-(diméthylamino)benzèneboronique
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Product Information

3-(Dimethylamino)phenylboronic acid hydrochloride is a versatile compound widely recognized for its applications in medicinal chemistry and organic synthesis. This boronic acid derivative is particularly valuable in the development of pharmaceuticals, where it serves as a key building block in the synthesis of biologically active molecules. Its unique ability to form reversible covalent bonds with diols makes it an essential reagent in the preparation of glycosylated compounds, which are crucial in the study of carbohydrate chemistry and drug design.

Additionally, 3-(Dimethylamino)phenylboronic acid hydrochloride is utilized in various research applications, including the development of targeted therapies for cancer and other diseases. Its compatibility with various reaction conditions and ease of handling further enhance its appeal to researchers and industry professionals alike. With its distinct properties and practical applications, this compound stands out as a reliable choice for those looking to innovate in the fields of medicinal chemistry and organic synthesis.

Synonyms
Chlorhydrate d'acide 3-(diméthylamino)benzèneboronique
CAS Number
1256355-23-3
Purity
98 - 105 % (dosage par titrage)
Molecular Formula
C8H12BNO2 · HCl
Molecular Weight
201.46
MDL Number
MFCD04112542
PubChem ID
44754897
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
Chlorhydrate d'acide 3-(diméthylamino)benzèneboronique
CAS Number
1256355-23-3
Purity
98 - 105 % (dosage par titrage)
Molecular Formula
C8H12BNO2 · HCl
Molecular Weight
201.46
MDL Number
MFCD04112542
PubChem ID
44754897
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Conserver entre 2 et 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

3-(Dimethylamino)phenylboronic acid hydrochloride is widely utilized in research focused on:

  • Drug Development: This compound serves as a key building block in the synthesis of various pharmaceuticals, particularly in the development of targeted cancer therapies. Its ability to form stable complexes with biomolecules enhances drug efficacy.
  • Bioconjugation: It is used in bioconjugation processes to attach drugs or imaging agents to antibodies or proteins, improving the delivery and specificity of treatments in fields like oncology and immunotherapy.
  • Organic Synthesis: Researchers employ this compound in organic synthesis as a versatile reagent for coupling reactions, which are essential in creating complex organic molecules for various applications.
  • Sensor Technology: The compound is also applied in the development of chemical sensors, particularly for detecting biomolecules, due to its high sensitivity and selectivity, making it valuable in diagnostics and environmental monitoring.
  • Material Science: In material science, it is utilized to modify surfaces and create functional materials, which can lead to advancements in electronics and nanotechnology, offering improved performance compared to traditional materials.

Citations