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双(乙腈)二氯钯(II)

产品号 10002 公司名称 Alfa Aesar
CAS号 14592-56-4 公司网站 http://www.alfa.com
分子式 C4H6Cl2N2Pd 电 话
分子量 259.42984 传 真
纯 度 Pd 40.5% 电子邮件
保 存 Chembase数据库ID: 288327

产品价格信息

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产品别名

标题
Bis(acetonitrile)dichloropalladium(II)
IUPAC标准名
palladium(2+) ion bis(acetonitrile) dichloride
IUPAC传统名
palladium(2+) ion bis(acetonitrile) dichloride
别名
cis-Dichlorobis(acetonitrile)palladium(II)

产品登记号

CAS号 14592-56-4
MDL号 MFCD00013122
EC号 238-637-3

产品性质

纯度 Pd 40.5%
外观 Powder
溶解度 Soluble in acetonitrile, acetone, chloroform
GHS危险品标识 GHS06
GHS危险声明 H331-H302-H312-H315-H319-H335
欧盟危险性物质标志 X
GHS警示性声明 P261-P305+P351+P338-P302+P352-P321-P405-P501A
危险公开号 20/21/22-36/37/38
安全公开号 9-26-36/37
TSCA收录
联合国危险货物等级 6.1
联合国危险货物编号 UN3439
联合国危险货物包装类别(PG) III

产品详细信息

参考文献

  • A 6:1 molar ratio of the high-temperature phase-transfer catalyst Tetraphenylphosphonium chloride, A10575, and the Pd complex, provides an effective catalyst for the Heck reaction of normally unreactive aryl halides, e.g. chlorobenzene with styrene to give stilbene. The reaction is performed at 140-150o in DMF or NMP in the presence of sodium acetate: Angew. Chem. Int. Ed., 37, 481 (1997).
  • Effective alternative catalyst to trans-Dichlorobis(triphenylphosphine)palladium(II), 10491, for the carbonylative cross-coupling of arylboronic acids with aryl iodides to give unsymmetrical benzophenones: Tetrahedron Lett., 34, 7595 (1993); see also Appendix 5.
  • Catalyses the cleavage of phenolic TBDMS ethers under mild conditions: Tetrahedron Lett., 37, 153 (1996), and, in the presence of 2-Bromomesitylene, A12277, promotes one-pot desilylation-oxidation of aliphatic silyl ethers to aldehydes or ketones: J. Org. Chem., 61, 2918 (1996); cf J. Org. Chem., 48, 1286 (1983).
  • Organic-soluble complex for catalysis of a variety of reactions, with the advantage over trans-Bis(benzonitrile)dichloropalladium(II), 10006, that the nitrile by-product, being volatile and water-miscible, is readily removed in the workup. In the presence of triethylamine, ortho-allylanilines undergo cyclization to indoles: J. Am. Chem. Soc., 98, 2674 (1976):