9-Nitroanthracene

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Names

[ CAS No. ]:
602-60-8

[ Name ]:
9-Nitroanthracene

[Synonym ]:
EINECS 210-021-9
MFCD00001248
Anthracene, 9-nitro-
9-Nitroanthracene

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Boiling Point ]:
402.9±14.0 °C at 760 mmHg

[ Melting Point ]:
144-144ºC

[ Molecular Formula ]:
C14H9NO2

[ Molecular Weight ]:
223.227

[ Flash Point ]:
200.4±12.9 °C

[ Exact Mass ]:
223.063324

[ PSA ]:
45.82000

[ LogP ]:
4.41

[ Vapour Pressure ]:
0.0±0.9 mmHg at 25°C

[ Index of Refraction ]:
1.742

[ Storage condition ]:
2-8°C

MSDS

Click to get detail MSDS

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
CB0715000
CHEMICAL NAME :
Anthracene, 9-nitro-
CAS REGISTRY NUMBER :
602-60-8
LAST UPDATED :
199510
DATA ITEMS CITED :
5
MOLECULAR FORMULA :
C14-H9-N-O2
MOLECULAR WEIGHT :
223.24
WISWESSER LINE NOTATION :
L C666J BNW

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

MUTATION DATA

TYPE OF TEST :
Mutation in mammalian somatic cells
TEST SYSTEM :
Human Lymphocyte
DOSE/DURATION :
3800 ug/L
REFERENCE :
MUREAV Mutation Research. (Elsevier Science Pub. B.V., POB 211, 1000 AE Amsterdam, Netherlands) V.1- 1964- Volume(issue)/page/year: 371,123,1996 *** REVIEWS *** IARC Cancer Review:Animal No Adequate Data IMEMDT IARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Man. (WHO Publications Centre USA, 49 Sheridan Ave., Albany, NY 12210) V.1- 1972- Volume(issue)/page/year: 33,179,1984 IARC Cancer Review:Human No Adequate Data IMEMDT IARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Man. (WHO Publications Centre USA, 49 Sheridan Ave., Albany, NY 12210) V.1- 1972- Volume(issue)/page/year: 33,179,1984 IARC Cancer Review:Group 3 IMSUDL IARC Monographs, Supplement. (WHO Publications Centre USA, 49 Sheridan Ave., Albany, NY 12210) No.1- 1979- Volume(issue)/page/year: 7,56,1987

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Safety Phrases ]:
S22-S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ RTECS ]:
CB0715000

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • Anthracene
  • Hexanitroethan
  • Anthracene,tetradecahydro-
  • 9-chloro-10-nitro-9,10-dihydroanthracene
  • 9,10-Dinitroanthracene
  • 9-ethoxy-10-nitro-9,10-dihydroanthracene
  • 9,9'-dinitro-9,9',10,10'-tetrahydro-10,10'-bianthryl
  • trifluoroacetic acid
  • cis-9,10-dinitro-9,10-dihydroanthracene

DownStream

  • Melitracen hydrochloride
  • 9,10-Dinitroanthracene
  • 9,10-Dibromo anthracene
  • 9-bromo-10-nitroanthracene
  • Anthrone
  • Dianthrone
  • Anthraquinone
  • 5,6-Dithiadecane
  • 9-butylsulfanylanthracene

Articles

Preparation, Structural Determination, and Characterization of Electronic Properties of Bis-silylated and Bis-germylated Lu3 N@Ih -C80.

Chemistry 21 , 16411-20, (2015)

Bis-silylated and bis-germylated derivatives of Lu3 N@Ih -C80 (3, 4, 5) were successfully synthesized by the photochemical addition of disiliranes 1 a, 1 b or digermirane 2, and fully characterized by...

9-Nitroanthracene derivative as a precursor of anthraquinone for photodynamic therapy.

Bioorg. Med. Chem. 15(11) , 3869-73, (2007)

Anthraquinones are typical photosensitizers used in photodynamic therapy (PDT). However, systemic toxicity is a major problem for anthraquinones due to their ability not only to bind DNA but also to c...

Xanthine oxidase-catalyzed DNA binding of dihydrodiol derivatives of nitro-polycyclic aromatic hydrocarbons.

Biochem. Biophys. Res. Commun. 141(1) , 245-50, (1986)

Xanthine oxidase, a mammalian nitroreductase, catalyzed the covalent binding of a series of nitro-polycyclic aromatic hydrocarbons (nitro-PAHs) trans-dihydrodiols to DNA. Some of the trans-dihydrodiol...


More Articles

Related Compounds

  • 9-NITROANTHRACENE
  • 9-nitroanthracene-d9
  • 2-methyl-9-nitroanthracene
  • 1-methyl-9-nitroanthracene
  • 9-bromo-10-nitroanthracene
  • 9-phenyl-10-nitroanthracene
  • 4-((Cyclohexylamino)methyl)benzoic acid hydrochloride
  • 1-[(2,4-Dichlorophenyl)methyl]-N-(1,1-dimethylethyl)-2-methyl-1H-indole-3-methanamine
  • 2-Methoxy-6-(pyrazol-1-yl)-benzonitrile
  • (R)-5-(1-(Methylamino)ethyl)nicotinic acid
  • 1H-3-Benzazepin-7-ol, 8-chloro-2,3,4,5-tetrahydro-5-(3-iodophenyl)-3-methyl-, (S)-
  • (4-Methyl-tetrahydro-furan-2-yl)-methanol
  • N-(1-cyanocyclopentyl)-2-[4-(4-fluorobenzenesulfonyl)-1,4-diazepan-1-yl]acetamide
  • 4,5,6,7-Tetrahydrobenzo[d]isoxazole-3-carbaldehyde
  • tert-Butyl-DL-alanine
  • 4-amino-N-[2-tert-butyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-benzimidazol-5-yl]-N-ethylbenzenesulfonamide