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Catalog Number:
39985
CAS Number:
885693-20-9
1-(tert-Butoxycarbonyl)-1,2,5,6-tetrahydro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
Purity:
≥ 98% (GC)
Synonym(s):
1-Boc-1,2,5,6-tetrahydro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine, 1-(tert-Butoxycarbonyl)-1,2,5,6-tetrahydro-3-pyridylboronic acid pinacol ester, 1-Boc-1,2,5,6-tetrahydro-3-pyridylboronic acid pinacol ester, 2-[1-(tert-Butoxycarbonyl)-1,2,5,6-tetrahydro-3-pyridyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Documents
$101.45 /200MG
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Product Information

1-(tert-Butoxycarbonyl)-1,2,5,6-tetrahydro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a versatile compound with significant applications in organic synthesis and medicinal chemistry. This compound is particularly valuable for researchers focused on developing novel pharmaceuticals, as its unique structure allows for the introduction of boron-containing moieties, which can enhance the biological activity of drug candidates. The presence of the tert-butoxycarbonyl (Boc) protecting group facilitates easy manipulation during synthetic processes, making it an ideal choice for complex molecule construction.

In addition to its utility in drug development, this compound can also serve as a key intermediate in the synthesis of various agrochemicals and functional materials. Its ability to form stable complexes with various substrates opens avenues for innovative applications in catalysis and materials science. Researchers and industry professionals will appreciate the compound's stability and ease of handling, which contribute to more efficient synthetic routes and improved yields in their projects.

Synonyms
1-Boc-1,2,5,6-tetrahydro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine, 1-(tert-Butoxycarbonyl)-1,2,5,6-tetrahydro-3-pyridylboronic acid pinacol ester, 1-Boc-1,2,5,6-tetrahydro-3-pyridylboronic acid pinacol ester, 2-[1-(tert-Butoxycarbonyl)-1,2,5,6-tetrahydro-3-pyridyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS Number
885693-20-9
Purity
≥ 98% (GC)
Molecular Formula
C16H28BNO4
Molecular Weight
309.21
MDL Number
MFCD10697911
PubChem ID
49835909
Melting Point
103 - 107 ?C
Appearance
White to light yellow crystalline powder
Conditions
Store at RT
General Information
Synonyms
1-Boc-1,2,5,6-tetrahydro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine, 1-(tert-Butoxycarbonyl)-1,2,5,6-tetrahydro-3-pyridylboronic acid pinacol ester, 1-Boc-1,2,5,6-tetrahydro-3-pyridylboronic acid pinacol ester, 2-[1-(tert-Butoxycarbonyl)-1,2,5,6-tetrahydro-3-pyridyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS Number
885693-20-9
Purity
≥ 98% (GC)
Molecular Formula
C16H28BNO4
Molecular Weight
309.21
MDL Number
MFCD10697911
PubChem ID
49835909
Melting Point
103 - 107 ?C
Appearance
White to light yellow 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

1-(tert-Butoxycarbonyl)-1,2,5,6-tetrahydro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as an intermediate in the synthesis of various pharmaceuticals, particularly in the development of new drugs targeting neurological disorders.
  • Organic Synthesis: It is employed in organic synthesis as a building block for creating complex molecules, making it valuable for chemists working on innovative chemical reactions.
  • Material Science: The compound is used in the formulation of advanced materials, including polymers and coatings, enhancing their properties such as durability and resistance to environmental factors.
  • Agricultural Chemicals: It finds application in the synthesis of agrochemicals, contributing to the development of more effective pesticides and herbicides that are safer for the environment.
  • Research in Catalysis: The compound is utilized in catalytic processes, improving reaction efficiency and selectivity in various chemical transformations, which is crucial for researchers aiming to optimize reaction conditions.

Citations