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CAS 132696-45-8

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(R)-3-(BOC-AMINO)-2-METHYLPROPIONIC ACID

Description:
(R)-3-(BOC-AMINO)-2-METHYLPROPIONIC ACID, with the CAS number 132696-45-8, is a chiral amino acid derivative characterized by the presence of a tert-butyloxycarbonyl (BOC) protecting group on the amino functional group. This compound features a branched aliphatic structure, which includes a methyl group and a propionic acid moiety, contributing to its unique stereochemistry. The BOC group is commonly used in peptide synthesis as a protective group for amino acids, allowing for selective reactions without interference from the amino group. The presence of the chiral center at the 3-position of the propionic acid backbone imparts specific optical activity, making it relevant in the synthesis of pharmaceuticals and biologically active compounds. Additionally, this compound is soluble in polar organic solvents, which facilitates its use in various chemical reactions and applications in organic synthesis. Its stability under standard laboratory conditions makes it a valuable intermediate in the preparation of more complex molecules.
Formula:C9H17NO4
InChI:InChI=1/C9H17NO4/c1-6(7(11)12)5-10-8(13)14-9(2,3)4/h6H,5H2,1-4H3,(H,10,13)(H,11,12)/t6-/m1/s1
SMILES:C[C@H](CN=C(O)OC(C)(C)C)C(=O)O
Synonyms:
  • Boc-R-3-Aminoisobutyric acid
  • Propanoic acid, 3-[[(1,1-dimethylethoxy)carbonyl]amino]-2-methyl-, (2R)- (9CI)
  • (R)-Boc-Β2-Homoala-Oh
  • 3-[[(1,1-Dimethylethoxy)Carbonyl]Amino]-2R-Methyl-Propanoic Acid
  • (2R)-3-[(tert-butoxycarbonyl)amino]-2-methylpropanoic acid
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