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Catalog Number:
40234
CAS Number:
89694-47-3
Acide 4-chloro-3-méthoxyphénylboronique
Purity:
98 - 105 % (dosage par titrage)
Synonym(s):
Acide 4-chloro-3-méthoxybenzèneboronique
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Product Information

4-Chloro-3-methoxyphenylboronic acid is a versatile boronic acid derivative that plays a crucial role in organic synthesis and medicinal chemistry. This compound is recognized for its ability to form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Researchers and industry professionals utilize this compound to synthesize a variety of biologically active molecules, including pharmaceuticals and agrochemicals. Its unique structure allows for selective functionalization, which is particularly beneficial in the development of targeted therapies and advanced materials.

The compound's properties, such as its solubility in organic solvents and compatibility with various reaction conditions, enhance its utility in laboratory settings. Additionally, 4-Chloro-3-methoxyphenylboronic acid serves as a key building block in the synthesis of complex organic compounds, enabling the creation of innovative solutions in drug discovery and development. Its application in the synthesis of heterocyclic compounds further underscores its significance in the field, making it a valuable asset for researchers aiming to explore new chemical entities.

Synonyms
Acide 4-chloro-3-méthoxybenzèneboronique
CAS Number
89694-47-3
Purity
98 - 105 % (dosage par titrage)
Molecular Formula
C7H8BClO3
Molecular Weight
186.4
MDL Number
MFCD01318965
PubChem ID
23005377
Melting Point
151 °C (lit.)
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Magasin chez RT
General Information
Synonyms
Acide 4-chloro-3-méthoxybenzèneboronique
CAS Number
89694-47-3
Purity
98 - 105 % (dosage par titrage)
Molecular Formula
C7H8BClO3
Molecular Weight
186.4
MDL Number
MFCD01318965
PubChem ID
23005377
Melting Point
151 °C (lit.)
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

4-Chloro-3-methoxyphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound is essential for creating complex organic molecules, particularly in the synthesis of pharmaceuticals and agrochemicals, due to its ability to form stable boronate esters.
  • Medicinal Chemistry: It plays a crucial role in drug development, especially in the design of inhibitors for various enzymes, making it valuable in the pharmaceutical industry for targeting diseases.
  • Materials Science: The compound is used in developing advanced materials, including polymers and nanomaterials, which can enhance properties such as conductivity and strength.
  • Bioconjugation: It is employed in bioconjugation techniques to attach biomolecules to surfaces or other molecules, facilitating research in biotechnology and diagnostics.
  • Analytical Chemistry: This chemical serves as a reagent in various analytical methods, helping researchers detect and quantify specific compounds in complex mixtures.

Citations