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Catalog Number:
39943
CAS Number:
68716-51-8
2-(3,5-Dichlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Purity:
≥ 98% (GC)
Synonym(s):
1,3-Dichloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene, 3,5-Dichlorophenylboronic acid pinacol ester
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Product Information

2-(3,5-Dichlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile boron-containing compound that finds significant applications in organic synthesis and medicinal chemistry. Known for its unique structure, this compound serves as a valuable reagent in cross-coupling reactions, particularly in the formation of carbon-carbon bonds. Its ability to selectively participate in reactions makes it an essential tool for researchers aiming to develop complex organic molecules, including pharmaceuticals and agrochemicals. The presence of the dichlorophenyl group enhances its reactivity, allowing for targeted modifications in synthetic pathways.

In addition to its synthetic utility, 2-(3,5-Dichlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is recognized for its stability and ease of handling, which are critical for laboratory applications. Researchers benefit from its compatibility with various reaction conditions, making it an ideal choice for both academic and industrial settings. Its unique properties not only streamline synthetic processes but also contribute to the development of innovative solutions in drug discovery and material science.

Synonyms
1,3-Dichloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene, 3,5-Dichlorophenylboronic acid pinacol ester
CAS Number
68716-51-8
Purity
≥ 98% (GC)
Molecular Formula
C12H15BCl2O2
Molecular Weight
272.96
MDL Number
MFCD05863906
PubChem ID
2758200
Melting Point
51 - 55 ?C
Appearance
White to off-white crystalline powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
1,3-Dichloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene, 3,5-Dichlorophenylboronic acid pinacol ester
CAS Number
68716-51-8
Purity
≥ 98% (GC)
Molecular Formula
C12H15BCl2O2
Molecular Weight
272.96
MDL Number
MFCD05863906
PubChem ID
2758200
Melting Point
51 - 55 ?C
Appearance
White to off-white crystalline powder
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-(3,5-Dichlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile reagent in the synthesis of various organic molecules, particularly in the formation of carbon-boron bonds, which are crucial in creating complex organic structures.
  • Agricultural Chemistry: It is employed in the development of new agrochemicals, enhancing crop protection formulations by improving the efficacy of active ingredients against pests and diseases.
  • Pharmaceutical Development: The compound is used in medicinal chemistry for the synthesis of potential drug candidates, particularly in the design of boron-containing pharmaceuticals that may exhibit unique biological activities.
  • Material Science: It plays a role in the creation of advanced materials, including polymers and composites, where its boron content can enhance thermal and mechanical properties.
  • Environmental Applications: This chemical is investigated for its potential in environmental remediation processes, particularly in the removal of pollutants through innovative boron-based technologies.

Citations