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化驗
97%
形狀
solid
mp
102-104 °C (lit.)
SMILES 字串
ClP(Cl)(=O)CP(Cl)(Cl)=O
InChI
1S/CH2Cl4O2P2/c2-8(3,6)1-9(4,5)7/h1H2
InChI 密鑰
VRXYCDTWIOCJBH-UHFFFAOYSA-N
一般說明
亚甲基双氯化磷是一种有机磷化合物,常用于膦酰化反应。相比POCl3,反应性更强,反应速率更快。这是由于CH2基的作用(lack of electron back-donation),造成磷原子中心的亲电性更强。
應用
亚甲基双(二氯膦酸)可用于以下研究:
- 麦考酚亚甲基双(膦酸)衍生物的合成。
- 核苷的膦酰化。
- P,P′-亚甲基双膦酸部分酯化物的制备。
- 亚甲基双膦酸对称双酯和对称四酯的合成。
訊號詞
Danger
危險聲明
危險分類
Eye Dam. 1 - Skin Corr. 1B
安全危害
儲存類別代碼
8A - Combustible corrosive hazardous materials
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
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Tetrahedron Letters, 46(!4), 2417-2421 (2005)
The Journal of organic chemistry, 78(2), 270-277 (2012-12-05)
A new transformation of methylene-bis(phosphonic dichloride) into tetrathiobisphosphonate derivatives is reported. The reaction of methylene-bis(phosphonic dichloride) with 1,2-ethanedithiol in bromoform in the presence of AlCl(3) formed methylene-bis(1,3,2-dithiaphospholane-2-sulfide), which gave rise to O,O'-diester-methylenediphosphonotetrathioate analogues 1a-k upon reaction with phenols and alkyl
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