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About This Item
Empirical Formula (Hill Notation):
C8H17NO3
CAS Number:
Molecular Weight:
175.23
Beilstein:
2206127
MDL number:
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.22
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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 Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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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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