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Catalog Number:
39921
CAS Number:
286961-15-7
1-Carbobenzoxy-1,2,3,6-tétrahydro-4-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)pyridine
Purity:
≥ 98% (CG)
Synonym(s):
Ester pinacol de l'acide 1-Cbz-1,2,3,6-tétrahydropyridine-4-boronique, Ester pinacolique de l'acide 1-benzyloxycarbonyl-1,2,3,6-tétrahydropyridine-4-boronique, 2-[1-(carbobenzoxy)-1,2,3,6-tétrahydro-4-pyridyl]-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane, Benzyl-4-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridine-1(2 H )-carboxylate
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Product Information

1-Carbobenzoxy-1,2,3,6-tetrahydro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a versatile compound with significant potential in organic synthesis and medicinal chemistry. This compound features a unique dioxaborolane moiety, which enhances its reactivity and stability, making it an excellent candidate for various chemical transformations. Its structure allows for applications in the development of pharmaceuticals, particularly in the synthesis of complex molecules where precision and efficiency are paramount.

Researchers and industry professionals can leverage this compound in the creation of targeted drug delivery systems and in the development of new therapeutic agents. Its ability to facilitate cross-coupling reactions positions it as a valuable tool in the synthesis of biologically active compounds. The compound's stability and reactivity profile also make it suitable for use in high-throughput screening applications, where rapid synthesis and evaluation of compounds are essential.

Synonyms
Ester pinacol de l'acide 1-Cbz-1,2,3,6-tétrahydropyridine-4-boronique, Ester pinacolique de l'acide 1-benzyloxycarbonyl-1,2,3,6-tétrahydropyridine-4-boronique, 2-[1-(carbobenzoxy)-1,2,3,6-tétrahydro-4-pyridyl]-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane, Benzyl-4-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridine-1(2 H )-carboxylate
CAS Number
286961-15-7
Purity
≥ 98% (CG)
Molecular Formula
C 19 H 26 BNO 4
Molecular Weight
343.23
MDL Number
MFCD11521562
PubChem ID
11290836
Melting Point
93 - 97 ?C
Appearance
Poudre cristalline blanche à jaune clair
Conditions
Conserver à ≤ -10 °C
General Information
Synonyms
Ester pinacol de l'acide 1-Cbz-1,2,3,6-tétrahydropyridine-4-boronique, Ester pinacolique de l'acide 1-benzyloxycarbonyl-1,2,3,6-tétrahydropyridine-4-boronique, 2-[1-(carbobenzoxy)-1,2,3,6-tétrahydro-4-pyridyl]-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane, Benzyl-4-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridine-1(2 H )-carboxylate
CAS Number
286961-15-7
Purity
≥ 98% (CG)
Molecular Formula
C 19 H 26 BNO 4
Molecular Weight
343.23
MDL Number
MFCD11521562
PubChem ID
11290836
Melting Point
93 - 97 ?C
Appearance
Poudre cristalline blanche à jaune clair
Conditions
Conserver à ≤ -10 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

1-Carbobenzoxy-1,2,3,6-tetrahydro-4-(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 a key intermediate in the synthesis of various pharmaceutical agents, particularly in the development of drugs targeting neurological disorders.
  • Organic Synthesis: It is employed in organic synthesis as a versatile building block, facilitating the creation of complex molecules with specific functional groups.
  • Material Science: The compound finds applications in the formulation of advanced materials, enhancing properties such as thermal stability and mechanical strength.
  • Catalysis: It can be used in catalytic processes, improving reaction efficiency and selectivity in organic transformations, making it valuable for chemists in both academic and industrial settings.
  • Research in Boron Chemistry: As a boron-containing compound, it contributes to the study of boron chemistry, which has implications in various fields including agriculture and environmental science.

Citations