15555
Boc-Nle-OH
≥99.0% (TLC)
Synonym(s):
(S)-2-(Boc-amino)caproic acid, (S)-2-(Boc-amino)hexanoic acid, Boc-L-norleucine
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About This Item
Empirical Formula (Hill Notation):
C11H21NO4
CAS Number:
Molecular Weight:
231.29
UNSPSC Code:
12352209
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
3608376
InChI
1S/C11H21NO4/c1-5-6-7-8(9(13)14)12-10(15)16-11(2,3)4/h8H,5-7H2,1-4H3,(H,12,15)(H,13,14)/t8-/m0/s1
SMILES string
CCCC[C@H](NC(=O)OC(C)(C)C)C(O)=O
InChI key
ZIOCIQJXEKFHJO-QMMMGPOBSA-N
assay
≥99.0% (TLC)
optical activity
[α]20/D −8±1°, c = 1% in methanol
reaction suitability
reaction type: Boc solid-phase peptide synthesis
application(s)
peptide synthesis
Quality Level
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
Regulatory Information
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Tianliang He et al.
Oncogene (2018-06-22)
The antiviral metabolites from bacterial stress response to bacteriophage infection can maintain homeostasis of host cells, while metabolism disorder is a remarkable characteristic of tumorigenesis. In the aspect of metabolic homeostasis, therefore, the antiviral homeostasis-maintaining metabolites of bacteria may possess
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