578428
(S)-(-)-5,5′,6,6′-四甲基-3,3′-二叔丁基-1,1′-联苯-2,2′-二醇
97%
方案
97%
表单
solid
旋光性
[α]20/D -83±3°, c = 0.4 in THF
mp
170-174 °C
SMILES字符串
Cc1cc(c(O)c(c1C)-c2c(C)c(C)cc(c2O)C(C)(C)C)C(C)(C)C
InChI
1S/C24H34O2/c1-13-11-17(23(5,6)7)21(25)19(15(13)3)20-16(4)14(2)12-18(22(20)26)24(8,9)10/h11-12,25-26H,1-10H3
InChI key
NMVVBVMYPLMIOU-UHFFFAOYSA-N
一般描述
(S)-5,5′,6,6′-Tetramethyl-3,3′-di-tert-butyl-1,1′-biphenyl-2,2′-diol, a biphenyl chiral ligand is used to prepare mono- and bidentate phosphites applicable as catalysts in the hydroformylation of allyl cyanide, heterocyclic olefins, and asymmetric hydrogenation of dimethyl itaconate.
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
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
Synthesis of new chiral monodentate phosphite ligands and their use in catalytic asymmetric hydrogenation
Hua Z, et al.
Organic Letters, 5(21), 3831-3834 (2003)
Asymmetric Hydroformylation of Heterocyclic Olefins Mediated by Supramolecularly Regulated Rhodium-Bisphosphite Complexes
Rovira L, et al.
The Journal of Organic Chemistry, 80(20), 10397-10403 (2015)
Synthesis and application of a new bisphosphite ligand collection for asymmetric hydroformylation of allyl cyanide
Cobley CJ, et al.
The Journal of Organic Chemistry, 69(12), 4031-4040 (2004)
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