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氯化铬(II), 无水_分子结构_CAS_10049-05-5)
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氯化铬(II), 无水

产品号 L14342 公司名称 Alfa Aesar
CAS号 10049-05-5 公司网站 http://www.alfa.com
分子式 Cl2Cr 电 话
分子量 122.9021 传 真
纯 度 97% 电子邮件
保 存 Chembase数据库ID: 302385

产品价格信息

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产品别名

标题
Chromium(II) chloride, anhydrous
IUPAC标准名
λ2-chromium(2+) ion dichloride
IUPAC传统名
λ2-chromium(2+) ion dichloride
别名
Chromous chloride

产品登记号

EC号 233-163-3
CAS号 10049-05-5
默克索引号 142244
MDL号 MFCD00010947

产品性质

纯度 97%
密度 2.878
熔点 824°C
GHS危险品标识 GHS05
GHS危险品标识 GHS07
GHS危险声明 H314-H318-H302
欧盟危险性物质标志 X
欧盟危险性物质标志 腐蚀性(Corrosive) 腐蚀性(Corrosive) (C)
GHS警示性声明 P260-P303+P361+P353-P305+P351+P338-P301+P330+P331-P405-P501A
危险公开号 22-34
RTECS编号 GB5250000
安全公开号 26-36/37/39-45
保存注意事项 Air & Moisture Sensitive
TSCA收录
联合国危险货物等级 8
联合国危险货物编号 UN3260
联合国危险货物包装类别(PG) III

产品详细信息

参考文献

  • With vinyl halides, forms vinyl Cr compounds which can add selectively to aldehydes to give allylic alcohols (Nozaki reaction): Tetrahedron Lett., 24, 5281 (1983). Better results have been obtained in the presence of a trace of NiCl2: J. Am. Chem. Soc., 108, 6048(1986). For similar reaction with alkynyl halides, see: Tetrahedron Lett., 26, 5585 (1985); Tetrahedron Lett., 28, 3463 (1987): Org. Synth. Coll., 9, 472 (1998). Intramolecular application of the Nozaki reaction has effected closure of a 13-membered ring: J. Am. Chem. Soc., 110, 5198 (1988), and of a strained 9-membered ring: J. Am. Chem. Soc., 112, 5369 (1992), in good yield. For brief reviews of CrCl2 as a reagent, see: J. Prakt. Chem./ Chem.-Ztg., 338, 491 (1996); Synlett, 722 (2001).
  • Reducing agent. Converts vic-dihalides and epoxides to alkenes, and ɑ-haloketones to ketones: J. Am. Chem. Soc., 82, 3399, 3696 (1960), reduces benzoquinones to hydroquinones: J. Chem. Soc. (C), 2349 (1969), and deoxygenates aromatic amine oxides: Chem. Pharm. Bull., 24, 1839 (1976). Alkyl nitro compounds are reduced to oximes: J. Chem. Soc. (C), 1182 (1970); Synthesis, 7 (1974). Aromatic nitro groups can be selectively reduced in DMF under mild conditions to arylamines, applicable to solid supported systems: Tetrahedron Lett., 40, 245 (1999).
  • Promotes the addition of allylic halides to aldehydes to give homoallylic alcohols, generally with high anti- selectivity (Hiyama reaction): Tetrahedron Lett., 22, 1037 (1981); 23, 2343 (1982); Tetrahedron, 37, 3873 (1981); J. Am. Chem. Soc., 113, 4218 (1991).