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Catalog Number:
39981
CAS Number:
331958-92-0
2-(3-Buten-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (stabilized with Phenothiazine)
Purity:
≥ 97% (GC)
Synonym(s):
(3-Buten-1-yl)boronic acid pinacol ester (stabilized with Phenothiazine)
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$58.39 /1G
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Product Information

2-(3-Buten-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, stabilized with Phenothiazine, is a versatile boron compound known for its unique reactivity and stability. This compound is particularly valuable in organic synthesis, serving as a key intermediate in the preparation of various organic molecules. Its structure allows for selective reactions, making it an excellent choice for researchers looking to develop new materials or pharmaceuticals. The stabilization with Phenothiazine enhances its shelf-life and usability, ensuring consistent performance in laboratory settings.

In practical applications, this compound is utilized in the synthesis of complex organic compounds, including pharmaceuticals and agrochemicals. Its ability to facilitate cross-coupling reactions makes it a preferred reagent in the development of advanced materials and fine chemicals. Researchers and industry professionals benefit from its efficiency and effectiveness, as it can significantly streamline synthetic pathways while minimizing by-products. With its unique properties and broad applicability, this compound is an essential tool for those engaged in cutting-edge chemical research and development.

Synonyms
(3-Buten-1-yl)boronic acid pinacol ester (stabilized with Phenothiazine)
CAS Number
331958-92-0
Purity
≥ 97% (GC)
Molecular Formula
C10H19BO2
Molecular Weight
182.07
MDL Number
MFCD11858602
PubChem ID
46739762
Density
0.89 g/mL
Appearance
Clear colorless liquid
Conditions
Store at RT
General Information
Synonyms
(3-Buten-1-yl)boronic acid pinacol ester (stabilized with Phenothiazine)
CAS Number
331958-92-0
Purity
≥ 97% (GC)
Molecular Formula
C10H19BO2
Molecular Weight
182.07
MDL Number
MFCD11858602
PubChem ID
46739762
Density
0.89 g/mL
Appearance
Clear colorless liquid
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-(3-Buten-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (stabilized with Phenothiazine) is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile reagent in organic chemistry, particularly in the synthesis of complex molecules, including pharmaceuticals and agrochemicals.
  • Cross-Coupling Reactions: It is employed in cross-coupling reactions, such as Suzuki-Miyaura reactions, facilitating the formation of carbon-carbon bonds, which is crucial in material science and drug development.
  • Polymer Chemistry: The compound is used in the production of boron-containing polymers, enhancing properties like thermal stability and mechanical strength, making it valuable in the plastics industry.
  • Fluorescent Probes: Its unique structure allows it to be utilized in the development of fluorescent probes for biological imaging, aiding researchers in studying cellular processes.
  • Environmental Applications: The compound can be used in the synthesis of environmentally friendly pesticides, contributing to sustainable agricultural practices by reducing chemical residues.

Citations