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About This Item
Linear Formula:
HOC6H3(NO2)CHO
CAS Number:
Molecular Weight:
167.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-587-0
Beilstein/REAXYS Number:
512565
MDL number:
Assay:
98%
InChI key
IHFRMUGEILMHNU-UHFFFAOYSA-N
InChI
1S/C7H5NO4/c9-4-5-3-6(8(11)12)1-2-7(5)10/h1-4,10H
SMILES string
[H]C(=O)c1cc(ccc1O)[N+]([O-])=O
assay
98%
Quality Level
functional group
aldehyde, nitro
Related Categories
General description
2-Hydroxy-5-nitrobenzaldehyde is a nitroaromatic compound used to prepare Schiff base ligands.
The interaction of 2-hydroxy-5-nitrobenzaldehyde and chlorogenic acid (CHL) with the components of the rat hepatic glucose 6-phosphatase system was studied.
The interaction of 2-hydroxy-5-nitrobenzaldehyde and chlorogenic acid (CHL) with the components of the rat hepatic glucose 6-phosphatase system was studied.
Free of 3-nitro isomer
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Anas G Elsafy et al.
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S 3483, a synthetic derivative of chlorogenic acid (CHL), was found to be a reversible, linear competitive inhibitor of the glucose-6-phosphatase (Glc-6-Pase) system in rat renal microsomes and rat and human liver microsomes. The Ki for S 3483 in rat
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Photodetection of originality and authentication of security documents such as money, passport, bank note, and national card have been a significant challenge in recent decade. Using of advanced optical systems could remarkably reduce copy and counterfeiting of such national and
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