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CAS 89536-84-5

:

Boc-N-methyl-D-leucine

Description:
Boc-N-methyl-D-leucine, with the CAS number 89536-84-5, is a protected amino acid commonly used in peptide synthesis. It features a tert-butyloxycarbonyl (Boc) group, which serves as a protective group for the amino functionality, allowing for selective reactions during the synthesis process. The "N-methyl" designation indicates that a methyl group is attached to the nitrogen atom of the amino group, which can influence the steric and electronic properties of the molecule. D-leucine refers to the specific stereochemistry of the leucine residue, which is the D-enantiomer, differing from its L counterpart in spatial arrangement. This compound is typically a white to off-white solid and is soluble in organic solvents like dimethyl sulfoxide (DMSO) and methanol, but less soluble in water. Its applications extend to the fields of medicinal chemistry and biochemistry, particularly in the development of peptide-based drugs and research involving protein synthesis. Proper handling and storage conditions are essential to maintain its stability and reactivity.
Formula:C12H23NO4
InChI:InChI=1/C12H23NO4/c1-8(2)7-9(10(14)15)13(6)11(16)17-12(3,4)5/h8-9H,7H2,1-6H3,(H,14,15)/t9-/m1/s1
SMILES:CC(C)C[C@H](C(=O)O)N(C)C(=O)OC(C)(C)C
Synonyms:
  • Boc-N-Me-D-Leu-OH
  • N-(tert-Butyloxycarbonyl)-N-methyl-D-leucine
  • N-(tert-butoxycarbonyl)-N-methyl-D-leucine
  • Boc-Nalpha-methyl-D-leucine
  • 4-methyl-2-[methyl-[(2-methylpropan-2-yl)oxy-oxomethyl]amino]pentanoic acid
  • (2R)-2-{[(tert-butoxy)carbonyl](methyl)amino}-4-methylpentanoic acid
  • Boc-
  • BOC-D-ALA(TBU)-OH
  • Boc-β-tBu-D-Ala-OH
  • BOC-D-LEU(ME)-OH
  • See more synonyms
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