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方案
≥98.0% (T)
旋光性
[α]20/D −10±1°, c = 1% in methanol
反应适用性
reaction type: solution phase peptide synthesis
mp
59-61 °C
应用
peptide synthesis
SMILES字符串
CC(O)=O.C[C@@H](OC(C)(C)C)[C@H](N)C(=O)OC(C)(C)C
InChI
1S/C12H25NO3.C2H4O2/c1-8(15-11(2,3)4)9(13)10(14)16-12(5,6)7;1-2(3)4/h8-9H,13H2,1-7H3;1H3,(H,3,4)/t8-,9+;/m1./s1
InChI key
BGAUVMFJRASONL-RJUBDTSPSA-N
其他说明
保护性苏氨酸，可用于多肽合成，例如糖肽的合成
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
Chernyak AYa et al.
Carbohydrate research, 216, 381-398 (1991-09-02)
The disaccharides alpha-L-Rhap-(1----3)-beta-D-GlcpA and beta-D-GlcpA-(1----3)-alpha-L-Rhap bearing amide-linked L-serine or L-threonine, which represent the repeating unit(s) of the capsular polysaccharide from E. coli O6:K54:H10, have been synthesised. O-tert-Butyl-protected amino acid tert-butyl esters were condensed with the corresponding biouronic acid as the
N.J. Forrow et al.
Tetrahedron Letters, 31, 3493-3493 (1990)
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