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Merck
CN

263524

2,3-二氟苯腈

98%

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线性分子式:
F2C6H3CN
化学文摘社编号:
分子量:
139.10
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
244-418-3
MDL number:
Assay:
98%
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产品名称

2,3-二氟苯腈, 98%

InChI key

GKPHNZYMLJPYJJ-UHFFFAOYSA-N

InChI

1S/C7H3F2N/c8-6-3-1-2-5(4-10)7(6)9/h1-3H

SMILES string

Fc1cccc(C#N)c1F

assay

98%

refractive index

n20/D 1.4882 (lit.)

density

1.254 g/mL at 25 °C (lit.)

functional group

fluoro
nitrile

Quality Level

Application

2,3-Difluorobenzonitrile has been used in the preparation of difluorophenyl-1,2,3,5-dithiadiazolyl and cyanophenoxazines.

General description

Electronic transitions of 2,3-difluorobenzonitrile has been studied by photoacoustic spectroscopy.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

167.0 °F - closed cup

flash_point_c

75 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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M Alcolea Palafox et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 57(12), 2373-2389 (2002-01-05)
Geometry, vibrational frequencies, atomic charges and several thermodynamic parameters (the total energy, the zero point energy, the rotational constants and the room temperature entropy) were calculated using ab initio quantum chemical methods for 2,3-difluorobenzonitrile molecule. The results were compared with
Cyano-activated fluoro displacement reactions in the synthesis of cyanophenoxazines and related compounds.
Eastmond GC, et al.
New. J. Chem., 25(3), 385-390 (2001)
The effect of fluorinated aryl substituents on the crystal structures of 1, 2, 3, 5-dithiadiazolyl radicals.
Clarke CS, et al.
CrystEngComm, 12(1), 172-185 (2010)
Two electronic transitions in the near-UV region of six isomeric difluorobenzonitriles-I.
Ramu K, et al.
Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy, 49(2), 223-236 (1993)

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