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Merck
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重要文件

D102008

Sigma-Aldrich

1,3-二氟苯

≥99%

同義詞:

1,3-二氟苯, 2,4-二氟苯, 间二氟苯

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About This Item

經驗公式(希爾表示法):
C6H4F2
CAS號碼:
分子量::
114.09
Beilstein:
1904537
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

≥99%

形狀

liquid

折射率

n20/D 1.438 (lit.)

bp

82 °C (lit.)

密度

1.163 g/mL at 25 °C (lit.)

SMILES 字串

Fc1cccc(F)c1

InChI

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

InChI 密鑰

UEMGWPRHOOEKTA-UHFFFAOYSA-N

尋找類似的產品? 前往 產品比較指南

象形圖

Flame

訊號詞

Danger

危險聲明

防範說明

危險分類

Flam. Liq. 2

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 1

閃點(°F)

35.6 °F

閃點(°C)

2 °C

個人防護裝備

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


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分析證明 (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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