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F10801

1-氟-2-硝基苯

Name: 1-氟-2-硝基苯
Brand: ALDRICH

99%

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关于此项目

线性分子式:

FC₆H₄NO₂

化学文摘社编号:

1493-27-2

分子量:

141.10

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24894745

EC Number:

216-088-0

Beilstein/REAXYS Number:

607262

MDL number:

MFCD00007048

Assay:

99%

Form:

liquid

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属性

assay

99%

form

liquid

refractive index

n20/D 1.532 (lit.)

bp

116 °C/22 mmHg (lit.)

mp

−9-−6 °C (lit.)

density

1.338 g/mL at 25 °C (lit.)

SMILES string

[O-][N+](=O)c1ccccc1F

InChI

1S/C6H4FNO2/c7-5-3-1-2-4-6(5)8(9)10/h1-4H

InChI key

PWKNBLFSJAVFAB-UHFFFAOYSA-N

说明

pictograms

GHS06,GHS08,GHS09

signalword

Danger

hcodes

H302 + H332,H311,H372,H411

pcodes

P273 - P280 - P301 + P312 - P302 + P352 + P312 - P304 + P340 + P312 - P314

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - STOT RE 1

存储类别

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

201.2 °F - closed cup

flash_point_c

94 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Spectroscopic, electronic structure and natural bond orbital analysis of o-fluoronitrobenzene and p-fluoronitrobenzene: a comparative study.

V Arjunan et al.

Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 84(1), 196-209 (2011-10-14)

Experimental FTIR, FT-Raman and FT-NMR spectroscopic studies of o-fluoronitrobenzene and p-fluoronitrobenzene have been carried out. A detailed quantum chemical calculations have been performed using DFT/B3LYP method with 6-311++G** and 6-31G** basis sets. Complete vibrational analyses of the compounds were performed.

[Parallelism between the kinetics of cross-reaction responses (anti-TNP and anti-DNP) and differences from the anti-LPS response when challenged with TNP-LPS immunization].

N Tuset et al.

Allergologia et immunopathologia, 14(6), 489-497 (1986-11-01)

The multi-functionality of a given antibody, even monoclonal antibody has recently been shown; this raises the possibility that the specificity of an antiserum be due to a population phenomena; i.e., the specificity would be the net result of the affinity

A new synthesis of amino acid-based enantiomerically pure substituted 2,3,4,4a,5,6-hexahydro-1H-pyrazino[1,2-a]quinoxalines.

Krishnananda Samanta et al.

Organic & biomolecular chemistry, 8(12), 2823-2828 (2010-04-24)

A new series of enantiomerically pure 2,3,4,4a,5,6-hexahydro-1H-pyrazino[1,2-a]quinoxalines were synthesized for the first time in twelve steps from 1-fluoro-2-nitrobenzene and S-amino acids with 13-20% overall yields. First use of intramolecular Mitsunobu cyclization for 1,2,3,4-tetrahydroquinoxalines followed by PPh(3)/I(2)/imidazole mediated 6-exo-tet cyclization were

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全球贸易项目编号

货号	GTIN
F10801-250G	04061832765853
F10801-50G	04061833611647