About This Item
推荐产品
质量水平
方案
96%
表单
solid
旋光性
[α]/D -34±4°, c = 1 in chloroform
mp
222-226 °C
官能团
phosphine
SMILES字符串
P(c7ccccc7)(c6ccccc6)c1c2ccc(c1)CCc3c(cc(cc3)CC2)P(c5ccccc5)c4ccccc4
InChI
1S/C40H34P2/c1-5-13-35(14-6-1)41(36-15-7-2-8-16-36)39-29-31-21-25-33(39)27-23-32-22-26-34(28-24-31)40(30-32)42(37-17-9-3-10-18-37)38-19-11-4-12-20-38/h1-22,25-26,29-30H,23-24,27-28H2
InChI key
GYZZZILPVUYAFJ-UHFFFAOYSA-N
应用
- Enantioselective reductive cyclization of 1,6-enynes via asymmetric hydrogenation in the presence of a rhodium catalyst to form alkylidene-substituted heterocycles.
- Asymmetric hydroboration of 3,3-disubstituted cyclopropenes to form 2,2-disubstituted cyclopropyl boronates.
- Asymmetric ring-opening reactions of azabenzonorbornadienes in the presence of zinc(II) triflate and palladium(II) acetate to form aminodihydronaphthalenes.
法律信息
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
其他客户在看
商品
P-Phos ligand family enhances catalysis, featuring atropisomeric biaryl bisphosphine with unique structural elements.
P-Phos ligand family enhances catalysis, featuring atropisomeric biaryl bisphosphine with unique structural elements.
P-Phos ligand family enhances catalysis, featuring atropisomeric biaryl bisphosphine with unique structural elements.
P-Phos ligand family enhances catalysis, featuring atropisomeric biaryl bisphosphine with unique structural elements.
我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系技术服务部门