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
Beilstein:
3608376
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
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
SMILES string
CCCC[C@H](NC(=O)OC(C)(C)C)C(O)=O
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
InChI key
ZIOCIQJXEKFHJO-QMMMGPOBSA-N
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), 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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