Cas no 81505-49-9 (N-Boc-6-hydroxy-DL-norleucine Methyl Ester)

N-Boc-6-hydroxy-DL-norleucine Methyl Ester is a chiral building block for peptide synthesis, offering high purity and stability. This compound facilitates the assembly of complex peptides with precise stereochemistry, making it an invaluable tool for research in pharmaceutical and biotech industries. Its ease of use and consistent performance contribute to efficient synthesis processes.
N-Boc-6-hydroxy-DL-norleucine Methyl Ester structure
81505-49-9 structure
Product Name:N-Boc-6-hydroxy-DL-norleucine Methyl Ester
CAS No:81505-49-9
MF:C12H23NO5
MW:261.314724206924
MDL:MFCD18384776
CID:1803755
PubChem ID:18786293
Update Time:2025-10-16

N-Boc-6-hydroxy-DL-norleucine Methyl Ester Chemical and Physical Properties

Names and Identifiers

    • Methyl 6-hydroxy-N-{[(2-methyl-2-propanyl)oxy]carbonyl}norleucina te
    • Boc-L-Ser(Tos)-OCH3
    • methyl N-(t-butoxycarbonyl)-O-tosyl-L-serinate
    • AK-49073
    • PubChem12168
    • methyl (2S)-2-[N-(t-butoxycarbonyl)amino]-3-(4-methylbenzenesulfonyl)-oxypropionate
    • Boc-Ser(Tos)-OCH3
    • Boc-Ser(Tos)-OMe
    • methyl (2S)-2-[(tert-butoxycarbonyl)amino]-3-(p-tolylsulfonyloxy)propionate
    • (S)-methyl 2-(tert-butoxycarbonylamino)-6-hydroxyhexanoate
    • (S)-(-)-Methyl 2-[(tert-butoxycarbonyl)amino]-6-hydroxypentanoate
    • methyl N-(tert-butoxycarbonyl)-O-[(4-methylphenyl)sulfonyl]serinate
    • KB-48416
    • methyl 3-(p-toluenesulfonyloxy)-2-(S)-(t-butoxycarbonylamino)propionate
    • BR-49073
    • N-Boc-L-Ser-(OTos)-OMe
    • methyl (2S)-2-[(tert-butoxycarbonyl)amino]-6-hydroxyhexanoate
    • N-Boc-6-hydroxy-DL-norleucine Methyl Ester
    • DL-Norleucine, N-[(1,1-dimethylethoxy)carbonyl]-6-hydroxy-, methyl ester (ZCI)
    • N-[(1,1-Dimethylethoxy)carbonyl]-6-hydroxynorleucine methyl ester (ACI)
    • Methyl 2-((tert-butoxycarbonyl)amino)-6-hydroxyhexanoate
    • N-Boc-6-hydroxy-DL-norleucine methyl ester (Boc-DL-Nle(OH)-OMe)
    • DB-087991
    • methyl 6-hydroxy-2-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoate
    • SCHEMBL4416484
    • AC6865
    • AKOS027257019
    • SY028579
    • CS-0319393
    • N-Boc-6-hydroxy-DL-norleucineMethylEster
    • MFCD18384776
    • 81505-49-9
    • MDL: MFCD18384776
    • Inchi: 1S/C12H23NO5/c1-12(2,3)18-11(16)13-9(10(15)17-4)7-5-6-8-14/h9,14H,5-8H2,1-4H3,(H,13,16)
    • InChI Key: RROCSCBJUBRRQV-UHFFFAOYSA-N
    • SMILES: O=C(NC(CCCCO)C(OC)=O)OC(C)(C)C

Computed Properties

  • Exact Mass: 261.15800
  • Monoisotopic Mass: 261.15762283g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 6
  • Heavy Atom Count: 18
  • Rotatable Bond Count: 10
  • Complexity: 272
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 0.9
  • Topological Polar Surface Area: 84.9?2

Experimental Properties

  • PSA: 88.35000
  • LogP: 1.41970

N-Boc-6-hydroxy-DL-norleucine Methyl Ester Pricemore >>

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N-Boc-6-hydroxy-DL-norleucine Methyl Ester Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Zinc ,  Ammonium chloride Catalysts: Copper(II) triflate Solvents: Ethanol ,  Water ;  3 h, rt; 1 h, rt; 2 h, rt
Reference
Cu(OTf)2-Promoted 1,4-Addition of Alkyl Bromides to Dehydroalanine
Shin, Jung-Ah; et al, Journal of Organic Chemistry, 2019, 84(7), 4558-4565

Production Method 2

Reaction Conditions
1.1 Reagents: Potassium carbonate ,  1,4-Diiodobutane Solvents: Dimethylformamide ;  4 h, rt
2.1 Reagents: Zinc ,  Ammonium chloride Catalysts: Copper(II) triflate Solvents: Ethanol ,  Water ;  3 h, rt; 1 h, rt; 2 h, rt
Reference
Cu(OTf)2-Promoted 1,4-Addition of Alkyl Bromides to Dehydroalanine
Shin, Jung-Ah; et al, Journal of Organic Chemistry, 2019, 84(7), 4558-4565

N-Boc-6-hydroxy-DL-norleucine Methyl Ester Raw materials

N-Boc-6-hydroxy-DL-norleucine Methyl Ester Preparation Products

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