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CAS No:28954-12-3
MF:C4H9NO3
Appearance:white or off-white crystalline powder
Specification:98.5%
UN number:-
Package:1/5/10/25kgs/drum
Supply Capacity:Tons
Synonyms:l-allothreonin;O-T-BUTYL-L-ALLO-THREONINE;H-ALLO-THR(BUT)-OH;H-ALLO-THR-O;H-ALLO-THR-OH;H-ALLO-THR(TBU)-OH;H-L-ALLO-THR-OH;L(+)-ALLO-THREONINE,"Allothreonine, L-","L-allo-threonine; L-Allothreonine; 28954-12-3; (2S,3S)-2-amino-3-hydroxybutanoic acid; allo-L-Threonine; HCQ253CKVK; Allothreonine, L-; CHEBI:28718; (S)-ALLOTHREONINE; (S)-ALLO-THREONINE; DTXSID10183151; NSC-206283; DTXCID20105642; 249-327-2; allothreonine; h-allo-thr-oh; DL-allo-Threonine; 144-98-9; L(+)-allo-Threonine; ALLO-THREONINE; MFCD00064268; rel-(2S,3S)-2-Amino-3-hydroxybutanoic acid; DL-allothreonine; (2S,3S)-2-ammonio-3-hydroxybutanoate; Threonine, allo-; Allothreonine, DL-; 4-04-00-03170 (Beilstein Handbook Reference); EINECS 249-327-2; UNII-HCQ253CKVK; NSC 206283; BRN 1721645; 29NAP6417F; DL-2-Amino-3-hydroxybutyric acid; MFCD00067248; NSC-41828; L-; allo; -Threonine; l-(+)-allothreonine; L-allo-Threonine, 99%; CHEMBL59238; SCHEMBL117301; orb1302114; DTXSID301030659; BCP08009; MSK169995; (2S,3S)-2-amino-3-hydroxybutanoate; AKOS015924200; CS-W008315; FA30577; FA48713; HY-W008315; AC-22377; AS-12250; SY024226; SY234191; (2s,3s)-2-amino-3-hydroxy-butyric acid; A1519; NS00074066; (2s 3s)-(+)-2-amino-3-hydroxybutyric acid; (2s,3s)-(+)-2-amino-3-hydroxybutyric acid; EN300-73665; thr; C05519; BUTANOIC ACID, 2-AMINO-3-ALLO-HYDROXY-; 9F03AEE4-59DA-4E42-B83D-06EE4AF23EAF; Q27103859; Z1162448524; L-allo-Threonine;(2S,3S)-2-Amino-3-hydroxybutyric acid",119.120,C4H9NO3,
Product application:L(+)-allo-Threonine L-allothreonine Suzhou Health Chemicals 28954-12-3 L-allo-Threonine manufacturer Chiral amino acid Pharmaceutical intermediates Globomycin synthesis Chiral building blocks Buy L-allo-Threonine L(+)-allo-Threonine price CAS 28954-12-3 supplier High purity L-allothreonine (2S,3S)-2-amino-3-hydroxybutanoic acid Peptide synthesis raw material L-allo-Threonine specification Custom synthesis amino acid
L(+)-allo-Threonine serves as a crucial non-proteinogenic chiral amino acid building block, playing a vital role in modern biopharmaceuticals and organic synthesis. It is predominantly utilized as a key pharmaceutical intermediate in the solid-phase and solution-phase peptide synthesis of novel cyclic peptide antibiotics, including Globomycin and its congener SF-1902 A5. Furthermore, owing to its unique stereocenters and dual-functional reactivity, it is widely employed as an indispensable chiral source for asymmetric synthesis, chiral ligand fabrication, and complex natural product total synthesis.