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Cyclopentylamine, 99%, Thermo Scientific Chemicals
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Catalog number L01966.22
also known as L01966-22
Price (USD)/ Each
115.00
-
Quantity:
100 g
Price (USD)/ Each
115.00
Cyclopentylamine, 99%, Thermo Scientific Chemicals
Catalog numberL01966.22
Price (USD)/ Each
115.00
-
Chemical Identifiers
CAS1003-03-8
IUPAC Namecyclopentanamine
Molecular FormulaC5H11N
InChI KeyNISGSNTVMOOSJQ-UHFFFAOYSA-N
SMILESNC1CCCC1
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Specifications
Specification Sheet
Specification SheetIdentification (FTIR)Conforms
Refractive Index1.4480-1.4510 @20?C
FormLiquid
Appearance (Color)Clear colorless to pale yellow
Assay (GC)≥98.5%
Cyclopentylamine acts as an important raw material and intermediate used in organic synthesis and pharmaceuticals. Further, it serves as chemokine receptor 2 antagonists. It acts as a ligand in coordination chemistry and forms cis-dichlorobis(cyclopentylamine)platinum(II) complex.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Cyclopentylamine acts as an important raw material and intermediate used in organic synthesis and pharmaceuticals. Further, it serves as chemokine receptor 2 antagonists. It acts as a ligand in coordination chemistry and forms cis-dichlorobis(cyclopentylamine)platinum(II) complex.
Solubility
Miscible with water, acetone and benzene.
Notes
Incompatible with strong oxidizing agents, acids, acid chlorides, acid anhydrides and carbon dioxide.
Cyclopentylamine acts as an important raw material and intermediate used in organic synthesis and pharmaceuticals. Further, it serves as chemokine receptor 2 antagonists. It acts as a ligand in coordination chemistry and forms cis-dichlorobis(cyclopentylamine)platinum(II) complex.
Solubility
Miscible with water, acetone and benzene.
Notes
Incompatible with strong oxidizing agents, acids, acid chlorides, acid anhydrides and carbon dioxide.
RUO – Research Use Only
General References:
- Qin, W. W.; Sang, C. Y.; Zhang, L. L.; Wei, W.; Tian, H. Z.; Liu, H. X.; Chen, S. W.; Hui, L. Synthesis and biological evaluation of 2,4-diaminopyrimidines as selective Aurora A kinase inhibitors. Eur. J. Med. Chem. 2015, 95, 174-184.
- Shackman, H. M.; Ding, W.; Bolgar, M. S. A Novel Route to Recognizing Quaternary Ammonium Cations Using Electrospray Mass Spectrometry. J. Am. Soc. Mass. Spectrom. 2015, 26 (1), 181-189.