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Merck
CN

D102008

Sigma-Aldrich

1,3-二氟苯

≥99%

别名:

1,3-二氟苯, 2,4-二氟苯, 间二氟苯

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About This Item

经验公式(希尔记法):
C6H4F2
CAS号:
分子量:
114.09
Beilstein:
1904537
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

≥99%

表单

liquid

折射率

n20/D 1.438 (lit.)

沸点

82 °C (lit.)

密度

1.163 g/mL at 25 °C (lit.)

SMILES字符串

Fc1cccc(F)c1

InChI

1S/C6H4F2/c7-5-2-1-3-6(8)4-5/h1-4H

InChI key

UEMGWPRHOOEKTA-UHFFFAOYSA-N

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象形图

Flame

警示用语:

Danger

危险声明

预防措施声明

危险分类

Flam. Liq. 2

储存分类代码

3 - Flammable liquids

WGK

WGK 1

闪点(°F)

35.6 °F

闪点(°C)

2 °C

个人防护装备

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

法规信息

危险化学品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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D Gala et al.
Journal of pharmaceutical sciences, 81(12), 1199-1203 (1992-12-01)
Alpha-Hydroxyaryl ketones such as 2-hydroxypropiophenone and 1-(2,4-difluorophenyl)-2-hydroxy-1-propanone, the key intermediates in the preparation of antifungal agents, decompose into oxidized, rearranged, and condensed products. These products were isolated and characterized. The possible mechanisms for the formation of the products are discussed.
Aujin Kim et al.
The Journal of organic chemistry, 71(5), 2170-2172 (2006-02-25)
A short, high-yielding synthesis of differentially substituted resorcinol derivatives has been developed that utilizes 1,3-difluorobenzene as the starting material and employs sequential nucleophilic aromatic substitution (S(N)Ar) reactions to generate desymmetrized products. The scope and limitations of the second S(N)Ar reaction

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