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CAS 143979-15-1

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Boc-L-2-allylglycine dicyclohexylamine salt

Description:
Boc-L-2-allylglycine dicyclohexylamine salt is a chemical compound that features a protected form of the amino acid L-2-allylglycine, where the amino group is protected by a tert-butyloxycarbonyl (Boc) group. This compound is typically used in peptide synthesis and other organic chemistry applications due to its ability to facilitate the formation of peptide bonds while preventing unwanted reactions at the amino group. The presence of the dicyclohexylamine salt enhances its solubility and stability in various solvents, making it suitable for laboratory use. The compound is characterized by its specific molecular structure, which includes an allyl side chain that can participate in further chemical reactions, such as cross-coupling or cyclization. Additionally, the Boc protecting group can be removed under acidic conditions, allowing for the subsequent functionalization of the amino acid. Overall, Boc-L-2-allylglycine dicyclohexylamine salt is a valuable intermediate in synthetic organic chemistry, particularly in the development of biologically active compounds.
Formula:C10H17NO4
InChI:InChI=1/C10H17NO4/c1-5-6-11(7-8(12)13)9(14)15-10(2,3)4/h5H,1,6-7H2,2-4H3,(H,12,13)
SMILES:C=CCN(CC(=O)O)C(=O)OC(C)(C)C
Synonyms:
  • Boc-Gly(Allyl)-Oh Dcha
  • Boc-L-Allylglycine-Dcha
  • Boc-L-Allylglycine Dcha Salt
  • Boc-L-Allylglycine Dicyclohexylaminesalt
  • Boc-L-Allylglycine Dicyclohexylammonium Salt
  • Boc-Algly-Oh Dcha
  • Boc-(Allyl)Gly-Oh Dcha
  • Boc-L-Allylglycine dicyclohexylamine
  • (2S)-2-[(tert-butoxycarbonyl)amino]pent-4-enoic acid - N-cyclohexylcyclohexanamine (1:1)
  • N-(tert-butoxycarbonyl)-N-prop-2-en-1-ylglycine
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