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CAS 73821-95-1

:

boc-L-aspartic acid 4-cyclohexyl ester

Description:
Boc-L-aspartic acid 4-cyclohexyl ester is a chemical compound characterized by its structure, which includes a Boc (tert-butyloxycarbonyl) protecting group attached to the amino group of L-aspartic acid, along with a cyclohexyl ester moiety at the carboxylic acid position. This compound is typically used in peptide synthesis and medicinal chemistry due to its ability to protect the amino group during reactions, thereby facilitating the selective modification of the carboxylic acid. The presence of the cyclohexyl group enhances lipophilicity, which can influence the compound's solubility and biological activity. It is a white to off-white solid, and its stability and reactivity can be affected by environmental conditions such as pH and temperature. As with many amino acid derivatives, it may exhibit specific optical activity due to its chiral nature. Safety data should be consulted for handling, as with all chemical substances, to ensure proper precautions are taken during use.
Formula:C15H25NO6
InChI:InChI=1/C15H25NO6/c1-15(2,3)22-14(20)16-11(9-12(17)18)13(19)21-10-7-5-4-6-8-10/h10-11H,4-9H2,1-3H3,(H,16,20)(H,17,18)/t11-/m0/s1
SMILES:CC(C)(C)OC(=N[C@@H](CC(=O)O)C(=O)OC1CCCCC1)O
Synonyms:
  • Boc-Asp(OcHex)-OH
  • BOC-Asp(OcHx)-OH
  • 2-[(Tert-Butoxycarbonyl)Amino]-4-(Cyclohexyloxy)-4-Oxobutanoic Acid (Non-Preferred Name)
  • (2S)-2-[(tert-butoxycarbonyl)amino]-4-(cyclohexyloxy)-4-oxobutanoic acid (non-preferred name)
  • (3S)-3-[(tert-butoxycarbonyl)amino]-4-(cyclohexyloxy)-4-oxobutanoic acid (non-preferred name)
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