CAS 313469-03-3
:10-N-Boc-amino-dec-1-ene
Description:
10-N-Boc-amino-dec-1-ene is a chemical compound characterized by its structure, which includes a decene backbone with a Boc (tert-butyloxycarbonyl) protecting group attached to an amino group. This compound typically features a double bond at the first position of the decane chain, contributing to its reactivity and potential applications in organic synthesis. The Boc group serves as a protective moiety for the amino functionality, allowing for selective reactions without interfering with the amine. This compound is often utilized in peptide synthesis and other organic transformations due to its ability to facilitate the introduction of amino groups while maintaining stability under various reaction conditions. Its molecular structure and properties make it a valuable intermediate in the development of pharmaceuticals and other biologically active compounds. As with many organic compounds, handling should be done with care, following appropriate safety protocols to mitigate any risks associated with its use.
Formula:C15H29NO2
InChI:InChI=1/C15H29NO2/c1-5-6-7-8-9-10-11-12-13-16-14(17)18-15(2,3)4/h5H,1,6-13H2,2-4H3,(H,16,17)
SMILES:C=CCCCCCCCCN=C(O)OC(C)(C)C
Synonyms:- 1X1& 1& Ovm9U1 [Wln]
- Carbamic acid, N-9-decen-1-yl-, 1,1-dimethylethyl ester
- Dec-9-en-1-ylcarbamic acid tert-butyl ester
- N-9-Decen-1-ylcarbamic acid 1,1-dimethylethyl ester
- tert-Butyl dec-9-en-1-ylcarbamate
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Found 3 products.
tert-Butyl dec-9-en-1-ylcarbamate
CAS:Formula:C15H29NO2Purity:90%Color and Shape:LiquidMolecular weight:255.3963tert-Butyl dec-9-en-1-ylcarbamate
CAS:<p>tert-Butyl dec-9-en-1-ylcarbamate</p>Purity:90% +(stabilized with TBC)Molecular weight:255.4g/mol10-N-Boc-Amino-dec-1-ene
CAS:Formula:C15H29NO2Purity:90.0%Color and Shape:LiquidMolecular weight:255.402



