物质信息
ID:722308
名称和标识
IUPAC标准名
{1-[2-(diphenylphosphanyl)naphthalen-1-yl]naphthalen-2-yl}diphenylphosphane
别名
(R)-(+)-BINAP(R)-(+)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl(R)-(+)-2,2'-联(二苯基膦基)-1,1'-联萘
IUPAC传统名
binap
化合物性质
理化性质
比旋光度
+230 (c=0.3 in toluene)
熔点
239-241°C
安全信息
欧盟危险性物质标志
刺激性 (Xi)危险公开号
36/37/38
GHS危险声明
H315-H319-H335
GHS警示性声明
P261-P305+P351+P338-P302+P352-P321-P405-P501A
TSCA收录
否
GHS危险品标识
急性毒性（口服，皮肤接触，吸入），类别4
皮肤刺激，类别2
眼刺激，类别2
皮肤过敏，类别1
特定目标器官毒性 -一次接触，类别3
安全公开号
26-37
保存注意事项
Air Sensitive
产品相关信息
纯度
98%
描述信息
暂无数据
点击上传数据
分子图谱
暂无数据
点击上传数据
参考文献
• Chiral chelating ligand which is the basis of a number of homogeneous catalysts which promote hydrogenation reactions with very high enantiomeric excesses. Rh complexes catalyze the asymmetric hydrogenation of ɑ-acylaminoacrylic acids: J. Am. Chem. Soc., 102, 7932 (1980), and the isomerization of allylamines to chiral enamines: J. Chem. Soc., Chem. Commun., 600 (1982); Synthesis, 665 (1991). Asymmetric hydrogenation of ?-keto esters is achieved with a Ru based catalyst: J. Org. Chem., 57, 6691 (1992). For preparation of a cycloocta-1,5-diene Rh complex and use in enantioselective hydrogenation reaction, see: Org. Synth. Coll., 8, 183 (1993). For a review of the use of Ru BINAP complexes in asymmetric hydrogenation, see: Acta Chem. Scand., 50, 380 (1996).
• Reviews: BINAP catalysis: Acc. Chem. Res., 23, 345 (1990); binaphthylic derivatives as chiral auxiliaries: Synthesis, 503 (1992); advances in biaryl-type biphosphne ligands: Tetrahedron, 61, 5405 (2005).