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Catalog Number:
40025
CAS Number:
1073354-70-7
1-(tert-Butoxycarbonyl)-3,5-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazole
Purity:
≥ 98% (HPLC)
Synonym(s):
1-Boc-3,5-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazole, 1-Boc-3,5-dimethylpyrazole-4-boronic acid pinacol ester, 1-(tert-Butoxycarbonyl)-3,5-dimethylpyrazole-4-boronic acidpinacol ester, tert-Butyl3,5-Dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole-1-carboxylate
Documents
$38.06 /200MG
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Product Information

1-(tert-Butoxycarbonyl)-3,5-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazole is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This compound features a unique structure that incorporates both a pyrazole ring and a dioxaborolane moiety, making it particularly valuable in the development of pharmaceuticals and agrochemicals. Its ability to facilitate various chemical reactions, such as cross-coupling reactions, positions it as a key intermediate in the synthesis of complex molecules. Researchers have found it beneficial in the design of novel drug candidates, especially in targeting specific biological pathways due to its functional groups that enhance solubility and bioavailability.

Moreover, this compound's stability and reactivity profile allow for its application in the synthesis of boron-containing compounds, which are increasingly important in materials science and catalysis. Its unique properties enable chemists to explore innovative pathways for creating new materials with tailored functionalities. The compound stands out in comparison to similar intermediates due to its enhanced selectivity and efficiency in reactions, making it an essential tool for researchers and industry professionals looking to advance their projects.

Synonyms
1-Boc-3,5-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazole, 1-Boc-3,5-dimethylpyrazole-4-boronic acid pinacol ester, 1-(tert-Butoxycarbonyl)-3,5-dimethylpyrazole-4-boronic acidpinacol ester, tert-Butyl3,5-Dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole-1-carboxylate
CAS Number
1073354-70-7
Purity
≥ 98% (HPLC)
Molecular Formula
C16H27BN2O4
Molecular Weight
322.21
MDL Number
MFCD09027070
PubChem ID
16218387
Melting Point
109 - 113 °C
Appearance
White to off-white crystalline powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
1-Boc-3,5-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazole, 1-Boc-3,5-dimethylpyrazole-4-boronic acid pinacol ester, 1-(tert-Butoxycarbonyl)-3,5-dimethylpyrazole-4-boronic acidpinacol ester, tert-Butyl3,5-Dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole-1-carboxylate
CAS Number
1073354-70-7
Purity
≥ 98% (HPLC)
Molecular Formula
C16H27BN2O4
Molecular Weight
322.21
MDL Number
MFCD09027070
PubChem ID
16218387
Melting Point
109 - 113 °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

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

  • Pharmaceutical Development: This compound serves as an intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders, enhancing drug efficacy and specificity.
  • Organic Synthesis: It is used in the development of complex organic molecules, allowing chemists to create diverse compounds with unique properties, which can lead to innovations in materials science.
  • Bioconjugation: The chemical is valuable in bioconjugation processes, where it helps in attaching biomolecules to surfaces or other molecules, improving the functionality of diagnostic tools and therapeutic agents.
  • Agricultural Chemistry: This compound can be utilized in the formulation of agrochemicals, contributing to the development of more effective pesticides and herbicides that are safer for the environment.
  • Research in Catalysis: It plays a role in catalysis research, aiding in the design of catalysts that enhance reaction rates and selectivity, which is crucial for sustainable chemical processes.

Citations