2,7-二硝基甲酚

2,7-二硝基甲酚名称

[ CAS 号 ]:
24824-27-9

[ 中文名 ]:
2,7-二硝基甲酚

[ 英文名 ]:
2,7-dinitronaphthalene

[中文别名 ]:

2,7-二硝基萘

[英文别名 ]:

2,7-dinitro-naphthalene
Naphthalene,2,7-dinitro
1,7-Dinitronaphthalin
2,7-DINITRONAPHTHALENE
2,7-Dinitronaphthalin
EINECS 246-480-7
2,5-DIMETHYLPHENYLACETONE

2,7-二硝基甲酚物理化学性质

[ 密度 ]:
1.481g/cm3

[ 沸点 ]:
413.5ºC at 760mmHg

[ 熔点 ]:
231-233ºC

[ 分子式 ]:
C₁₀H₆N₂O₄

[ 分子量 ]:
218.16600

[ 闪点 ]:
216.6ºC

[ 精确质量 ]:
218.03300

[ PSA ]:
91.64000

[ LogP ]:
3.70260

[ 蒸汽压 ]:
1.14E-06mmHg at 25°C

[ 折射率 ]:
1.704

2,7-二硝基甲酚MSDS

2,7-二硝基甲酚毒性和生态

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

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2,7-二硝基甲酚安全信息

[ 个人防护装备 ]:
Eyeshields;Gloves

[ 危险品运输编码 ]:
UN 2811

[ RTECS号 ]:
QJ4552500

[ 包装等级 ]:
III

[ 危险类别 ]:
6.1(b)

[ 海关编码 ]:
2904209090

2,7-二硝基甲酚合成路线

2,7-二硝基甲酚上下游产品

2,7-二硝基甲酚上游产品

2,7-二硝基甲酚下游产品

2,7-二硝基甲酚海关

[ 海关编码 ]: 2904209090

[ 中文概述 ]:
2904209090 其他仅含硝基或亚硝基的衍生物。监管条件:无。增值税率:17.0%。退税率:9.0%。最惠国关税:5.5%。普通关税:30.0%

[ 申报要素 ]: 品名, 成分含量, 用途

[ 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%

2,7-二硝基甲酚文献

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)

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