おすすめの製品
品質水準
アッセイ
96%
mp
196-198 °C (lit.)
官能基
chloro
fluoro
SMILES記法
[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
シグナルワード
Warning
危険有害性情報
危険有害性の分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
ターゲットの組織
Respiratory system
保管分類コード
11 - Combustible Solids
WGK
WGK 3
引火点(°F)
Not applicable
引火点(℃)
Not applicable
個人用保護具 (PPE)
dust mask type N95 (US), Eyeshields, Gloves
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
Jan Code
374067-5G:
374067-BULK:
374067-VAR:
374067-25G:
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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
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
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
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
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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