4-nitrocatechol structure
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Common Name | 4-nitrocatechol | ||
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CAS Number | 3316-09-4 | Molecular Weight | 155.108 | |
Density | 1.6±0.1 g/cm3 | Boiling Point | 358.2±32.0 °C at 760 mmHg | |
Molecular Formula | C6H5NO4 | Melting Point | 173-177 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 168.8±13.6 °C |
Use of 4-nitrocatechol4-Nitrocatechol is a potent lipoxygenase inhibitor[1]. |
Name | 4-nitrocatechol |
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Synonym | More Synonyms |
Description | 4-Nitrocatechol is a potent lipoxygenase inhibitor[1]. |
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Related Catalog | |
Target |
Human Endogenous Metabolite Microbial Metabolite |
References |
Density | 1.6±0.1 g/cm3 |
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Boiling Point | 358.2±32.0 °C at 760 mmHg |
Melting Point | 173-177 °C(lit.) |
Molecular Formula | C6H5NO4 |
Molecular Weight | 155.108 |
Flash Point | 168.8±13.6 °C |
Exact Mass | 155.021851 |
PSA | 86.28000 |
LogP | 1.68 |
Vapour Pressure | 0.0±0.8 mmHg at 25°C |
Index of Refraction | 1.668 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
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Hazard Codes | Xi:Irritant; |
Risk Phrases | R36/37/38 |
Safety Phrases | S26 |
RIDADR | 2811 |
WGK Germany | 3 |
Packaging Group | III |
Hazard Class | 6.1(b) |
HS Code | 2908999090 |
Precursor 10 | |
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DownStream 10 | |
HS Code | 2908999090 |
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Summary | 2908999090 halogenated, sulphonated, nitrated or nitrosated derivatives of phenols or phenol-alcohols。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:5.5%。General tariff:30.0% |
Effect of commercially available green and black tea beverages on drug-metabolizing enzymes and oxidative stress in Wistar rats.
Food Chem. Toxicol. 70 , 120-7, (2014) The effect of commercially available green tea (GT) and black tea (BT) drinks on drug metabolizing enzymes (DME) and oxidative stress in rats was investigated. Male Wistar rats were fed a laboratory c... |
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Molecular characterization of the boron adducts of the proteasome inhibitor bortezomib with epigallocatechin-3-gallate and related polyphenols.
Org. Biomol. Chem. 13(13) , 3887-99, (2015) The green tea polyphenol epigallocatechin-3-gallate (EGCG) was reported to effectively antagonize the ability of Bortezomib (BZM) to induce apoptosis in cancer cells. This interaction was attributed t... |
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Phase II metabolism in human skin: skin explants show full coverage for glucuronidation, sulfation, N-acetylation, catechol methylation, and glutathione conjugation.
Drug Metab. Dispos. 43(1) , 126-39, (2014) Although skin is the largest organ of the human body, cutaneous drug metabolism is often overlooked, and existing experimental models are insufficiently validated. This proof-of-concept study investig... |
EINECS 222-009-0 |
1,2-Benzenediol, 4-nitro- |
1,2-dihydroxy-4-nitrobenzene |
[14C]-4-Nitrocatechol |
NITROCATECHOL (MIX OF ISOMERS) |
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3,4-dihydroxynitrobenzene |
4-Nitro-1,2-benzenediol |
4-nitrocatechol |
4-Nitrobenzol-1,2-diol |
MFCD00007242 |
4-Nitropyrocatechol |
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