All Photos(2)
About This Item
Linear Formula:
ClC6H3(NO2)OH
CAS Number:
Molecular Weight:
173.55
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
assay
97%
form
powder
mp
105-106 °C (lit.)
SMILES string
Oc1ccc(cc1Cl)[N+]([O-])=O
InChI
1S/C6H4ClNO3/c7-5-3-4(8(10)11)1-2-6(5)9/h1-3,9H
InChI key
BOFRXDMCQRTGII-UHFFFAOYSA-N
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signalword
Warning
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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α-L-Fucosidase (AFU) is a promising therapeutic target for the treatment of inflammation, cancer, cystic fibrosis, and fucosidosis. Some of the existing analytical methods for the assessment of AFU activity are lacking in sensitivity and selectivity, since most of them are
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Applied and environmental microbiology, 85(14) (2019-05-06)
The yeast Kluyveromyces lactis has been a successful host for the production of heterologous proteins for over 30 years. Currently, the galactose-/lactose-inducible and glucose-repressible LAC4 promoter (P
H Schulz et al.
Mikrobiologiia, 51(3), 402-406 (1982-05-01)
The coefficients of distribution of flavofungin, flavopentin, nigrofungin and brunefungin, antifungal antibiotics, carbonyl-conjugated pentaenes, between water and Saccharomyces cerevisiae cells were determined. The coefficients were shown to increase with a decrease in the cell concentration. Therefore, the minimal concentrations of
[Solubility of carbonyl-conjugated pentaenes in organic solvents and the effect of water].
H Schultz et al.
Antibiotiki, 27(1), 11-15 (1982-01-01)
G I Konoshenko et al.
Antibiotiki, 27(9), 687-693 (1982-01-01)
When used in concentrations of 10-15 micrograms per 10(8) cells, flavofungin and nigrofungin, carbonyl-conjugated pentaenes lowered the rate of oxygen absorption by thymocyte suspensions in the presence of glucose. Flavopentin inhibited glucose oxidation in higher concentrations. ADP and succinate did
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