15466
Boc-Aib-OH
≥99.0% (T)
Synonym(s):
α-(Boc-amino)isobutyric acid, Boc-α-methylalanine
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About This Item
Linear Formula:
(CH3)3CO2CNHC(CH3)2CO2H
CAS Number:
Molecular Weight:
203.24
Beilstein/REAXYS Number:
1953772
EC Number:
MDL number:
UNSPSC Code:
12352200
eCl@ss:
32160406
PubChem Substance ID:
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Quality Level
assay
≥99.0% (T)
form
solid
reaction suitability
reaction type: Boc solid-phase peptide synthesis
mp
118-122 °C
application(s)
peptide synthesis
SMILES string
CC(C)(C)OC(=O)NC(C)(C)C(O)=O
InChI
1S/C9H17NO4/c1-8(2,3)14-7(13)10-9(4,5)6(11)12/h1-5H3,(H,10,13)(H,11,12)
InChI key
MFNXWZGIFWJHMI-UHFFFAOYSA-N
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Other Notes
Protected unusual and seldom-occurring achiral amino acid.[1]
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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W. Mayr et al.
Liebigs Ann. Chem., 715-715 (1980)
John R Horsley et al.
Journal of the American Chemical Society, 136(35), 12479-12488 (2014-08-15)
Electrochemical studies are reported on a series of peptides constrained into either a 310-helix (1-6) or β-strand (7-9) conformation, with variable numbers of electron rich alkene containing side chains. Peptides (1 and 2) and (7 and 8) are further constrained
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