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1434127-01-1 | tert-butyl N-[(3S,4S)-3-fluoropiperidin-4-yl]carbamate

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Purchase CAS:1434127-01-1 | tert-butyl N-[(3S,4S)-3-fluoropiperidin-4-yl]carbamate,view related peer-reviewed papers,technical documents,similar products,MSDS & more.Molecular Structure AnalysisThe molecular formula of “tert-butyl N-[(3S,4S)-3-fluoropiperidin-4-yl]carbamate” is C10H20N2O3 . The exact mass is 216.14739250 g/mol . The compound has 2 hydrogen bond donors and 4 hydrogen bond acceptors . The compound has a complexity of 225 ....
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CAS:1434127-01-1 | tert-butyl N-[(3S,4S)-3-fluoropiperidin-4-yl]carbamate,Description

 

Molecular Structure Analysis

The molecular formula of “tert-butyl N-[(3S,4S)-3-fluoropiperidin-4-yl]carbamate” is C10H20N2O3. The exact mass is 216.14739250 g/mol. The compound has 2 hydrogen bond donors and 4 hydrogen bond acceptors. The compound has a complexity of 225.

 

Physical And Chemical Properties Analysis

The compound has a molecular weight of 216.28 g/mol. It has a topological polar surface area of 73.6 Ų. The compound has a rotatable bond count of 3. The physical form of a similar compound, “tert-butyl N-[(3S,4S)-3-aminooxan-4-yl]carbamate”, is a white to yellow solid.

Scientific Research Applications

 

  • Synthesis and Chemical Transformation :
    • Zhao et al. (2017) detailed the synthesis of a tert-butyl carbamate derivative, emphasizing its role as an intermediate in biologically active compounds like omisertinib (Zhao, Guo, Lan, & Xu, 2017).
    • Tang et al. (2014) synthesized (R)-tert-butyl carbamate as an intermediate of jaspine B, a natural product with cytotoxic activity against human carcinoma cell lines (Tang, Liu, Qin, Wang, Li, Huang, & Wang, 2014).
    • Sakaitani and Ohfune (1990) discussed the chemoselective transformation of amino protecting groups via tert-butyldimethylsilyl carbamates, highlighting their utility in organic synthesis (Sakaitani & Ohfune, 1990).
  • Biological and Pharmacological Applications :
    • Camarillo-López et al. (2020) explored a tert-butyl carbamate derivative’s potential in treating Alzheimer's disease, focusing on its β-secretase and acetylcholinesterase inhibitory activities (Camarillo-López, Hernández Rodríguez, Torres-Ramos, Arciniega-Martínez, García-Marín, Correa Basurto, Méndez Méndez, & Rosales-Hernández, 2020) .
    • Ghosh, Cárdenas, and Brindisi (2017) described enantioselective syntheses of tert-butyl carbamate derivatives for potential use as protease inhibitors (Ghosh, Cárdenas, & Brindisi, 2017).
  • Chemical Structure and Properties :
    • Kant, Singh, and Agarwal (2015) conducted synthetic and crystallographic studies on tert-butyl carbamate derivatives, offering insights into their molecular structure and interactions (Kant, Singh, & Agarwal, 2015).
    • Zheng et al. (2008) analyzed the crystal structure of a tert-butyl carbamate derivative to better understand its molecular conformation (Zheng, Huang, Guo, Zhang, & Jin, 2008).

More Information

Product Name:tert-butyl N-[(3S,4S)-3-fluoropiperidin-4-yl]carbamate
Synonyms:tert-butyl N-[(3S,4S)-3-fluoropiperidin-4-yl]carbamate;N-[(3S,4S)-3-Fluoro-4-piperidinyl]carbamic acid 1,1-dimethylethyl ester;(3S,4S)-4-(BOC-AMINO)-3-FLUOROPIPERIDINE;Carbamic acid, N-[(3S,4S)-3-fluoro-4-piperidinyl]-, 1,1-dimethylethyl ester;(S)-1-tert-butyl 3-methyl tetrahydropyridazine-1,3(2H)-dicarboxylate;tert-butyl ((3S,4S)-3-fluoropiperidin-4-yl)carbamate;(3S,4S)-N-Boc-3-fluoro-4-aminopiperidine
CAS:1434127-01-1
MF:C10H19FN2O2
MW:218.27
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Mol File:1434127-01-1.mol
 
tert-butyl N-[(3S,4S)-3-fluoropiperidin-4-yl]carbamate Chemical Properties
Boiling point 313.3±42.0 °C(Predicted)
density 1.08±0.1 g/cm3(Predicted)
pka11.24±0.40(Predicted)

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