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质量水平
检测方案
96%
mp
196-198 °C (lit.)
SMILES字符串
[Na+].[O-]C(=O)C(F)(F)Cl
InChI
1S/C2HClF2O2.Na/c3-2(4,5)1(6)7;/h(H,6,7);/q;+1/p-1
InChI key
MRTAVLDNYYEJHK-UHFFFAOYSA-M
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
J W Harris et al.
Chemical research in toxicology, 4(2), 180-186 (1991-03-01)
1,2-Dichloro-1,1-difluoroethane (HCFC-132b) is a potential substitute for some ozone-depleting chlorofluorocarbons and a model for other 1,1,1,2-tetrahaloethanes under consideration as chlorofluorocarbon substitutes. Male Fischer 344 rats were given 10 mmol/kg HCFC-132b dissolved in corn oil by intraperitoneal injection. An NMR assay
Keith R Solomon et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2(1), 62-67 (2003-03-28)
Increased UV-B through stratospheric ozone depletion leads to an increased chemical activity in the lower atmosphere (the troposphere). The effect of stratospheric ozone depletion on tropospheric ozone is small (though significant) compared to the ozone generated anthropogenically in areas already
M L Hanson et al.
Environmental toxicology and chemistry, 20(12), 2758-2767 (2002-01-05)
Chlorodifluoroacetic acid (CDFA) is a novel haloacetic acid (HAA) and has been recently documented in aquatic systems. It is a suspected degradation product of the refrigerants 1,1,2-trichloro-1,1-difluoroethane (CFC-113) and 1-chloro-1,1-difluoroethane (HCFC-142b). Haloacetic acids can be phytotoxic, putatively acting through inhibition
M Zdanowska-Fraczek et al.
Solid state nuclear magnetic resonance, 6(2), 141-146 (1996-04-01)
The reorientation of CClF2 groups in N(CH3)4H(ClF2CCOO)2 has been studied using pulsed NQR and NMR techniques. The temperature dependence of both chlorine (35Cl) NQR and fluorine (19F) NMR spin-lattice relaxation has been measured T1Q of chlorine is attributed to the
Jian Zheng et al.
Chemical communications (Cambridge, England), 49(68), 7513-7515 (2013-07-19)
A key intermediate, difluoromethylene phosphobetaine, in the Wittig reaction of ClCF2CO2Na-Ph3P with aldehydes was synthesized and characterized, which confirmed the reaction mechanism. The decarboxylation of this stable intermediate was a convenient approach for Wittig difluroolefination. Its reactivity could be adjusted
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