20646
O-tert-Butyl-L-threonine tert-butyl ester acetate salt
≥98.0% (T)
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About This Item
Empirical Formula (Hill Notation):
C12H25NO3 · C2H4O2
CAS Number:
Molecular Weight:
291.38
UNSPSC Code:
12352209
NACRES:
NA.22
PubChem Substance ID:
EC Number:
227-464-9
Beilstein/REAXYS Number:
6707078
MDL number:
InChI key
BGAUVMFJRASONL-RJUBDTSPSA-N
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
SMILES string
CC(O)=O.C[C@@H](OC(C)(C)C)[C@H](N)C(=O)OC(C)(C)C
assay
≥98.0% (T)
optical activity
[α]20/D −10±1°, c = 1% in methanol
reaction suitability
reaction type: solution phase peptide synthesis
mp
59-61 °C
application(s)
peptide synthesis
Other Notes
Protected threonine for peptide synthesis, e.g. of glycopeptides
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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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