CAS 510754-90-2
:tert-butyl (9-aminononyl)carbamate
Description:
Tert-butyl (9-aminononyl)carbamate is an organic compound characterized by its carbamate functional group, which consists of a tert-butyl group attached to a nonylamine moiety. This compound typically exhibits properties such as being a solid or viscous liquid at room temperature, depending on its specific formulation and purity. It is generally soluble in organic solvents, while its solubility in water may be limited due to the hydrophobic nature of the tert-butyl and nonyl groups. The presence of the amino group suggests potential reactivity, particularly in forming hydrogen bonds or participating in nucleophilic reactions. Tert-butyl (9-aminononyl)carbamate may be utilized in various applications, including as a reagent in organic synthesis or as an intermediate in the production of pharmaceuticals and agrochemicals. Safety considerations should be taken into account, as with many organic compounds, including proper handling and storage to avoid exposure. Overall, its unique structure and functional groups contribute to its utility in chemical synthesis and research.
Formula:C14H30N2O2
InChI:InChI=1/C14H30N2O2/c1-14(2,3)18-13(17)16-12-10-8-6-4-5-7-9-11-15/h4-12,15H2,1-3H3,(H,16,17)
SMILES:CC(C)(C)OC(=NCCCCCCCCCN)O
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Found 5 products.
Carbamic acid,N-(9-aminononyl)-, 1,1-dimethylethyl ester
CAS:Formula:C14H30N2O2Purity:97%Color and Shape:SolidMolecular weight:258.4002Nonane-1,9-diamine, N1-BOC protected
CAS:Nonane-1,9-diamine, N1-BOC protectedFormula:C14H30N2O2Purity:97%Color and Shape: pale yellow semi- solidMolecular weight:258.4002g/moltert-Butyl (9-aminononyl)carbamate
CAS:Formula:C14H30N2O2Purity:97%Color and Shape:Low Melting SolidMolecular weight:258.406tert-Butyl (9-aminononyl)carbamate
CAS:<p>Versatile small molecule scaffold</p>Formula:C14H30N2O2Purity:Min. 95%Molecular weight:258.4 g/moltert-Butyl (9-aminononyl)carbamate
CAS:<p>tert-Butyl (9-aminononyl)carbamate is an alkane chain featuring a terminal amine and a Boc-protected amino group. It serves as a PROTAC linker in the synthesis of PROTACs and various coupling applications. The amine can react with carboxylic acids, activated NHS esters, and carbonyl groups (ketones, aldehydes). The Boc group can be deprotected under mild acidic conditions to form a free amine.</p>Formula:C14H30N2O2Color and Shape:SolidMolecular weight:258.4




