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Merck

34125

Sigma-Aldrich

二溴二氟甲烷

≥95.0% (GC)

别名:

Carbon dibromide difluoride, Difluorodibromomethane

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About This Item

经验公式(希尔记法):
CBr2F2
CAS号:
分子量:
209.82
Beilstein:
1732515
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

蒸汽密度

7.24 (vs air)

品質等級

蒸汽壓力

12.79 psi ( 20 °C)

化驗

≥95.0% (GC)

形狀

liquid

折射率

n20/D 1.398 (lit.)
n20/D 1.398

bp

22-23 °C (lit.)

mp

−142-−141 °C (lit.)

密度

2.297 g/mL at 25 °C (lit.)

官能基

bromo
fluoro

儲存溫度

2-8°C

SMILES 字串

FC(F)(Br)Br

InChI

1S/CBr2F2/c2-1(3,4)5

InChI 密鑰

AZSZCFSOHXEJQE-UHFFFAOYSA-N

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一般說明

The photolysis products of dibromodifluoromethane were characterized by matrix isolation infrared and UV/Visible spectroscopy. Free radical addition of dibromodifluoromethane with fluoroolefins has been reported. Dibromodifluoromethane reacts with hydrocarbon olefins to yield 1,3-dibromo-1,1-difluoroalkene. Sulfinatodehalogenation reagent promoted addition reaction of difluorodibromomethane with alkenes, alkynes and cyclic enol ethers has been described.

應用

  • Synthesis of 3‑Fluoropyrazoles via Radical-Polar Crossover Photoinduced Cyclization: This study highlights the use of dibromodifluoromethane (CF2Br2) for the synthesis of valuable difluorinated and monofluorinated compounds through a novel photoinduced cyclization process (MA Reed, ND Patil, Synfacts, 2023).

其他說明

作为反应物与羰基化合物通过 Wittig 烯化反应转化成二氟亚甲基或氟亚甲基衍生物;二氟卡宾的前体

象形圖

Exclamation mark

訊號詞

Warning

危險分類

Eye Irrit. 2 - Ozone 1 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Gloves


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分析证书(COA)

Lot/Batch Number

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访问文档库

S. Hayaski et al.
Chemistry Letters (Jpn), 983-983 (1979)
Addition reactions of dibromodifluoromethane promoted by sulfinatodehalogenation reagents.
Wu F-H, et al.
Journal of Fluorine Chemistry, 80(2), 91-94 (1996)
Lisa George et al.
The Journal of chemical physics, 132(8), 084503-084503 (2010-03-03)
The photolysis products of dibromodifluoromethane (CF(2)Br(2)) were characterized by matrix isolation infrared and UV/Visible spectroscopy, supported by ab initio calculations. Photolysis at wavelengths of 240 and 266 nm of CF(2)Br(2):Ar samples (approximately 1:5000) held at approximately 5 K yielded iso-CF(2)Br(2)
H.P. Fritz et al.
Zeitschrift fur Naturforschung, B: Chemical Sciences, 86, 1375-1375 (1981)
Free Radical Additions Involving Fluorine Compounds. I. The Addition of Dibromodifluoromethane to Hydrocarbon Olefins.
Tarrant P and Lovelace AM.
Journal of the American Chemical Society, 76(13), 3466-3468 (1954)

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