Identification | More | [Name]
Boc-N-Methyl-L-isoleucine | [CAS]
52498-32-5 | [Synonyms]
BOC-L-MEILE-OH BOC-L-MELLE-OH BOC-MEILE-OH BOC-MELLE-OH BOC-N-ALPHA-METHYL-L-ISOLEUCINE BOC-N-ME-ILE-OH BOC-N-ME-ISOLEUCINE BOC-N-METHYL-L-ILE-OH BOC-N-METHYL-L-ISOLEUCINE N-ALPHA-T-BOC-N-ALPHA-METHYL-L-ISOLEUCINE N-ALPHA-T-BUTOXYCARBONYL-N-ALPHA-METHYL-L-ISOLEUCINE N-ALPHA-T-BUTYLOXYCARBONYL-N-ALPHA-METHYL-L-ISOLEUCINE N-ALPHA-TERT-BUTYLOXYCARBONYL-N-ALPHA-METHYL-L-ISOLEUCINE N-ALPHA-TERT-BUTYLOXYCABONYL-N-ALPHA-METHYL-L-ISOLEUCINE N-alpha-t-Butyloxycarbonyl-N-alpha-methy-L-isoleucine NALPHA-tert-Butoxycarbonyl-N-methyl-L-isoleucine N-tert-Butyloxycarbonyl-N-methyl-L-isoleucine | [Molecular Formula]
C12H23NO4 | [MDL Number]
MFCD00066105 | [Molecular Weight]
245.32 | [MOL File]
52498-32-5.mol |
Hazard Information | Back Directory | [Chemical Properties]
White powder | [Uses]
Boc-N-methyl-L-isoleucine (Boc-N-Me-Ile-OH) is a peptide products and can be used as a precursor in organic synthesis and pharmaceuticals[1]. | [References]
[1] KazuhiroIrie, et al. Isolation and biosynthesis of (?)-indolactam I, a new congener of indole alkaloid tumor promoter teleocidins. Tetrahedron Letters, 1990, 7337-7340. |
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