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About This Item
Linear Formula:
O2NC6H4CH2ONH2 · HCl
CAS Number:
Molecular Weight:
204.61
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
218-228-6
Beilstein/REAXYS Number:
3709565
MDL number:
Assay:
≥98.5% (AT)
Form:
crystals
Quality Level
assay
≥98.5% (AT)
form
crystals
mp
215 °C (dec.) (lit.)
functional group
nitro
SMILES string
Cl.NOCc1ccc(cc1)[N+]([O-])=O
InChI
1S/C7H8N2O3.ClH/c8-12-5-6-1-3-7(4-2-6)9(10)11;/h1-4H,5,8H2;1H
InChI key
LKCAFSOYOMFQSL-UHFFFAOYSA-N
Other Notes
Reagent for the preparation of N-(4-nitrobenzyloxy)-amino acids as substrates for an unambiguous N-hydroxypeptide synthesis
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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T D Traylor et al.
Journal of chromatography, 272(1), 9-20 (1983-01-14)
A new quantitative procedure for the high-performance liquid chromatographic (HPLC) resolution of human brain gangliosides employing reversed-phase chromatography is described. To provide a derivative which can be determined by UV absorption techniques, p-nitrobenzyloxyamine was coupled to the gangliosides. Derivatization involves
Joo Hyun Lim et al.
Frontiers in microbiology, 9, 2333-2333 (2018-10-16)
2-Deoxy-scyllo-inosose (DOI) has been a valuable starting natural product for the manufacture of pharmaceuticals or chemical engineering resources such as pyranose catechol. DOI synthase, which uses glucose-6-phosphate (Glc6P) as a substrate for DOI biosynthesis, is indispensably involved in the initial
Kenneth P Roberts et al.
Chemical research in toxicology, 19(2), 300-309 (2006-02-21)
A new method has been developed to accurately measure apurinic and apyrimidinic (AP) DNA damage sites, which are lesions in DNA formed by loss of a nucleobase from oxidative stress or carcinogen adducts. If AP sites are left unrepaired (or
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 73200-1G | 04061832867137 |
| 73200-5G | 04061835158225 |