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D102504

1,5-二氟-2,4-二硝基苯

Name: 1,5-二氟-2,4-二硝基苯
Brand: ALDRICH

97%

别名:

DFDNB

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关于此项目

线性分子式:

F₂C₆H₂(NO₂)₂

化学文摘社编号:

327-92-4

分子量:

204.09

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24893327

EC Number:

206-324-0

Beilstein/REAXYS Number:

1883116

MDL number:

MFCD00007052

Assay:

97%

Form:

powder

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属性

assay

97%

form

powder

mp

72-74 °C (lit.)

SMILES string

[O-][N+](=O)c1cc(c(F)cc1F)[N+]([O-])=O

InChI

1S/C6H2F2N2O4/c7-3-1-4(8)6(10(13)14)2-5(3)9(11)12/h1-2H

InChI key

VILFTWLXLYIEMV-UHFFFAOYSA-N

说明

pictograms

GHS06,GHS08

signalword

Danger

hcodes

H300,H311 + H331,H373

pcodes

P260 - P280 - P301 + P310 - P302 + P352 + P312 - P304 + P340 + P311 - P314

Hazard Classifications

Acute Tox. 2 Oral - Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - STOT RE 2

存储类别

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Benzofused tricycles based on 2-quinoxalinol.

Gang Liu et al.

Journal of combinatorial chemistry, 9(1), 70-78 (2007-01-09)

This paper describes our recent efforts to synthesize novel compound scaffolds integrating 2-quinoxalinol with privileged structures of 1,3-dihydro-benzoimidazol-2-one, 1,3-dihydro-benzoimidazole-2-thione, 3-hydroxy-1H-quinoxalin-2-one, 2H-benzo[1,4]oxazin-3-ol, 2H-benzo[1,4]thiazin-3-ol, and 1,3,4,5-tetrahydro-benzo[1,4]diazepin-2-one, respectively. Eight novel benzofused tricycles and their substituent diversity points were developed. These include pyrazino[2,3-g]quinoxaline-2,8-diol (I)

Scaffold-directed and traceless synthesis of tricyclic quinoxalinone imidazoles under microwave irradiation: for SCS-09 special issue-combinatorial approaches to drug discovery.

Suman Thummanagoti et al.

Molecular diversity, 15(1), 101-107 (2010-03-20)

Traceless synthesis of 2-aminoimidazoquinoxalinones has been performed on soluble polymer support under open-vessel microwave dielectric heating. The reaction progression is monitored directly by the conventional proton NMR which indicated no release of the substrate from the support. Fmoc-deprotected amino acid

Substituent diversity-directed synthesis of indole derivatives.

Dong Mei Wang et al.

Journal of combinatorial chemistry, 11(4), 556-575 (2009-05-28)

This paper reports a versatile, good-yielding, solution-phase method that is a substituent diversity-directed synthesis of 1H-indoles (6-13, 17-20) and 1-hydroxyindoles (14, 15) starting from commercially available 1,5-difluoro-2,4-dinitrobenzene. The synthetic products possessed the maximum six diversity points.

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全球贸易项目编号

货号	GTIN
D102504-10G	04061838353641