2-Amino-4-Nitroanisole
2-Amino-4-Nitroanisole structure
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Common Name | 2-Amino-4-Nitroanisole | ||
|---|---|---|---|---|
| CAS Number | 99-59-2 | Molecular Weight | 168.150 | |
| Density | 1.3±0.1 g/cm3 | Boiling Point | 351.8±22.0 °C at 760 mmHg | |
| Molecular Formula | C7H8N2O3 | Melting Point | 117-119 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 166.6±22.3 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Removal of multi-substituted nitroaromatic pollutants by zero valent iron: a comparison of performance, kinetics, toxicity and mechanisms.
Phys. Chem. Chem. Phys. 17 , 22072-8, (2015) Reductive degradation of three typical multi-substituted nitroaromatic pollutants by zero valent iron was comprehensively compared in terms of performance, kinetics, toxicity and mechanisms in this study. The results showed that 0.5 mM 2,4-dinitrochlorobenzen... |
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Microbial toxicity of the insensitive munitions compound, 2,4-dinitroanisole (DNAN), and its aromatic amine metabolites.
J. Hazard. Mater. 262 , 281-7, (2013) 2,4-Dinitroanisole (DNAN) is an insensitive munitions compound considered to replace conventional explosives such as 2,4,6-trinitrotoluene (TNT). DNAN undergoes facile microbial reduction to 2-methoxy-5-nitroaniline (MENA) and 2,4-diaminoanisole (DAAN). This ... |
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Synthesis and antitumor activity of 5-(9-acridinylamino)anisidine derivatives.
Bioorg. Med. Chem. 13(23) , 6513-20, (2005) A series of 5-(9-acridinylamino)anisidines were synthesized by condensing methoxy-substituted 1,3-phenylenediamines (10 and 11) with 9-chloroacridine derivatives to form 5-(9-acridinylamino)-m-anisidines (AMAs, 14a-e) and 5-(9-acridinylamino)-o-anisidines (AO... |
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(Bio)transformation of 2,4-dinitroanisole (DNAN) in soils.
J. Hazard. Mater. 304 , 214-21, (2015) Recent studies have begun to assess the environmental fate and toxicity of 2,4-dinitroanisole (DNAN), an insensitive munition compound of interest to defense agencies. Aerobic and anaerobic DNAN biotransformation in soils was evaluated in this study. Under ae... |
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5-Nitro-ortho-anisidine.
IARC Monogr. Eval. Carcinog. Risk Chem. Hum. 27 , 133-9, (1982)
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A Weibull model for the estimation of tumorigenic potency.
Biometrics 49(2) , 367-77, (1993) In this paper, a new method of estimating tumorigenic potency is proposed that takes into account information on survival and, when available, the underlying cause of death. Specifically, Weibull distributions are used to describe the time to tumor occurrence... |
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Calculation of carcinogenic potency from long-term animal carcinogenesis experiments.
Biometrics 40(1) , 27-40, (1984) An index of carcinogenic potency for chemicals tested in chronic animal experiments is described. By analogy with the well-known 'lethal dose 50' (LD50) of quantal bioassay, a 'tumorigenic dose 50' (TD50) may be defined (in the absence both of tumors in the c... |
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Disperse dyes derived from 2-methoxy-5-nitroaniline. Otutu JO and Osabohien E.
Orient. J. Chem. 25(4) , 863, (2009)
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