20644
O-tert-Butyl-L-threonine
≥98.0% (T)
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About This Item
Empirical Formula (Hill Notation):
C8H17NO3
CAS Number:
Molecular Weight:
175.23
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352209
MDL number:
Beilstein/REAXYS Number:
2206127
Product Name
O-tert-Butyl-L-threonine, ≥98.0% (T)
InChI
1S/C8H17NO3/c1-5(6(9)7(10)11)12-8(2,3)4/h5-6H,9H2,1-4H3,(H,10,11)/t5-,6+/m1/s1
SMILES string
C[C@@H](OC(C)(C)C)[C@H](N)C(O)=O
InChI key
NMJINEMBBQVPGY-RITPCOANSA-N
assay
≥98.0% (T)
optical activity
[α]20/D −43±2°, c = 1% in H2O
reaction suitability
reaction type: solution phase peptide synthesis
application(s)
peptide synthesis
Quality Level
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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Sajjad Ahmad et al.
Drug design, development and therapy, 15, 1299-1313 (2021-04-02)
Organocatalytic asymmetric Michael addition is a strong approach for C-C bond formation. The objective of the study is to design molecules by exploiting the efficiency of Michael Adducts. We proceeded with the synthesis of Michael adducts by tailoring the substitution
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