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CAS 107202-43-7

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(3S)-3-(N-Boc-amino)-4-phenyl-1-butene

Description:
(3S)-3-(N-Boc-amino)-4-phenyl-1-butene is an organic compound characterized by its specific stereochemistry and functional groups. The "N-Boc" (tert-butyloxycarbonyl) group indicates that it is a protected amine, commonly used in peptide synthesis to temporarily shield the amino group from reactions. The presence of a phenyl group suggests that the compound has aromatic characteristics, which can influence its reactivity and solubility. The butene moiety indicates that it contains a double bond, contributing to its unsaturation and potential for further chemical reactions, such as addition or polymerization. The stereochemistry at the 3-position is crucial for its biological activity and interactions, as chirality can significantly affect how the molecule behaves in biological systems. Overall, this compound is likely to be of interest in medicinal chemistry and organic synthesis, particularly in the development of pharmaceuticals or as an intermediate in complex organic reactions.
Formula:C15H21NO2
InChI:InChI=1/C15H21NO2/c1-5-13(11-12-9-7-6-8-10-12)16-14(17)18-15(2,3)4/h5-10,13H,1,11H2,2-4H3,(H,16,17)/t13-/m1/s1
SMILES:C=C[C@H](Cc1ccccc1)N=C(O)OC(C)(C)C
Synonyms:
  • (S)-3-Boc-amino-4-phenyl-1-butene
  • [(1S)-1-(Phenylmethyl)-2-propenyl]carbamic Acid1,1-Dimethylethyl Ester
  • N-[(1S)-1-(Phenylmethyl)-2-propen-1-yl]carbamic Acid ,1-Dimethylethyl Ester
  • tert-butyl [(1S)-1-benzylprop-2-en-1-yl]carbamate
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