15035
(Boc-aminooxy)acetic acid
≥98.0% (T)
Synonym(s):
N-Boc-(carboxymethoxy)amine
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About This Item
Linear Formula:
(CH3)3CO2CNHOCH2CO2H
CAS Number:
Molecular Weight:
191.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
6137646
Assay:
≥98.0% (T)
Form:
powder
Quality Level
assay
≥98.0% (T)
form
powder
mp
~115 °C (dec.)
functional group
amine, carboxylic acid
SMILES string
CC(C)(C)OC(=O)NOCC(O)=O
InChI
1S/C7H13NO5/c1-7(2,3)13-6(11)8-12-4-5(9)10/h4H2,1-3H3,(H,8,11)(H,9,10)
InChI key
QBXODCKYUZNZCY-UHFFFAOYSA-N
Application
(Boc-aminooxy)acetic acid was used in the preparation of Boc-aminooxy tetra(ethylene glycol).
Other Notes
Employed to introduce a hydroxylamine moiety into peptides; reaction with an aldehyde to an oxime.
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Storage Class
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Mariarosaria De Simone et al.
Contrast media & molecular imaging, 11(6), 561-571 (2017-01-05)
Superparamagnetic iron oxide nanoparticles (SPIONs) have received increasing interest as contrast media in biomedical imaging and innovative therapeutic tools, in particular for loco-regional ablative treatments and drug delivery. The future of therapeutic applications would strongly benefit from improving the capability
J. Shao et al.
Journal of the American Chemical Society, 117, 3893-3893 (1995)
O. Nyanguile et al.
Lett. Pept. Sci., 1, 9-9 (1994)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 15035-5G | 04061838738776 |
| 15035-1G | 04061825590998 |