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15555

Sigma-Aldrich

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:
6404-28-0
Molecular Weight:
231.29
Beilstein/REAXYS Number:
3608376
MDL number:
MFCD00037270
UNSPSC Code:
12352209
PubChem Substance ID:
57647494
NACRES:
NA.22

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

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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