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2,7-dinitronaphthalene

Names

[ CAS No. ]:
24824-27-9

[ Name ]:
2,7-dinitronaphthalene

[Synonym ]:
2,7-dinitro-naphthalene
Naphthalene,2,7-dinitro
1,7-Dinitronaphthalin
2,7-DINITRONAPHTHALENE
2,7-Dinitronaphthalin
EINECS 246-480-7
2,5-DIMETHYLPHENYLACETONE

Chemical & Physical Properties

[ Density]:
1.481g/cm3

[ Boiling Point ]:
413.5ºC at 760mmHg

[ Melting Point ]:
231-233ºC

[ Molecular Formula ]:
C10H6N2O4

[ Molecular Weight ]:
218.16600

[ Flash Point ]:
216.6ºC

[ Exact Mass ]:
218.03300

[ PSA ]:
91.64000

[ LogP ]:
3.70260

[ Vapour Pressure ]:
1.14E-06mmHg at 25°C

[ Index of Refraction ]:
1.704

MSDS

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
QJ4552500
CHEMICAL NAME :
Naphthalene, 2,7-dinitro-
CAS REGISTRY NUMBER :
24824-27-9
LAST UPDATED :
199206
DATA ITEMS CITED :
1
MOLECULAR FORMULA :
C10-H6-N2-O4
MOLECULAR WEIGHT :
218.18

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

MUTATION DATA

TYPE OF TEST :
Mutation test systems - not otherwise specified
TEST SYSTEM :
Bacteria - Escherichia coli
DOSE/DURATION :
10 ug/tube
REFERENCE :
EMMUEG Environmental and Molecular Mutagenesis. (Alan R. Liss, Inc., 41 E. 11th St., New York, NY 10003) V.10- 1987- Volume(issue)/page/year: 18,41,1991

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves

[ RIDADR ]:
UN 2811

[ RTECS ]:
QJ4552500

[ Packaging Group ]:
III

[ Hazard Class ]:
6.1(b)

[ HS Code ]:
2904209090

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2904209090

[ Summary ]:
2904209090 derivatives containing only nitro or only nitroso groups。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:5.5%。General tariff:30.0%

Articles

Electron transfer within charge-localized dinitroaromatic radical anions.

J. Phys. Chem. A 113(27) , 7730-6, (2009)

Rate constants for the intramolecular electron-transfer reaction in the 2,7-dinitronaphthalene (2(-)), 4,4'-dinitrotolane (3(-)), and 2,2'-dimethyl-4,4'-dinitrobiphenyl (4(-)) radical anions in severa...

Selectivity in capillary electrochromatography using native and single isomer anionic cyclodextrin reagents.

Anal. Chem. 72(1) , 88-95, (2000)

Separations of naphthalene compounds that differ in position of substitution and type of substituent were accomplished using cyclodextrin distribution capillary electrochromatography. Separation syste...

107. The further nitration of 1: 3-, 1: 6-, 2: 6-, and 2: 7-dinitronaphthalenes, and the preparation of 1: 3: 6-trinitronaphthalene. Edward, R.

J. Chem. Soc. , 533-34, (1946)


More Articles


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