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20644

Sigma-Aldrich

O-tert-Butyl-L-threonine

≥98.0% (T)

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About This Item

Empirical Formula (Hill Notation):
C8H17NO3
CAS Number:
4378-13-6
Molecular Weight:
175.23
Beilstein/REAXYS Number:
2206127
MDL number:
MFCD00037766
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
57647850
NACRES:
NA.22

Quality Level

100

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

SMILES string

C[C@@H](OC(C)(C)C)[C@H](N)C(O)=O

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

InChI key

NMJINEMBBQVPGY-RITPCOANSA-N

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
BCCJ2672
BCBG3786V
383959/1
314144/1

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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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