668486
(+)-1,2-双[(2S,5S)-2,5-二乙基膦烷基]苯
Namena purity
别名:
(2S,2′S,5S,5′S)-2,2′,5,5′-四乙基-1,1′-(邻亚苯基)二磷烷, (S,S)-乙基-DUPHOS
登录 查看组织和合同定价。
选择尺寸
关于此项目
经验公式（希尔记法）:
C22H36P2
化学文摘社编号:
分子量:
362.47
UNSPSC Code:
12352005
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
4814174
SMILES string
CC[C@H]1CC[C@H](CC)P1c2ccccc2P3[C@@H](CC)CC[C@@H]3CC
InChI key
GVVCHDNSTMEUCS-MUGJNUQGSA-N
InChI
1S/C22H36P2/c1-5-17-13-14-18(6-2)23(17)21-11-9-10-12-22(21)24-19(7-3)15-16-20(24)8-4/h9-12,17-20H,5-8,13-16H2,1-4H3/t17-,18-,19-,20-/m0/s1
refractive index
n20/D 1.581
density
1.010 g/mL at 25 °C
functional group
phosphine
Quality Level
Legal Information
与Namena Corp.合作销售，仅用于研究目的。这些化合物是根据E.I.du Pont de Nemours and Company的许可证生产和销售的，该许可证不包括在制药领域生产销售产品时使用这些化合物的权利。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Assymetric synthesis of (2S, 3R)-and (2S, 3S)-[2-13C; 3-2H] glutamic acid
Okuma K, et al.
Tetrahedron Letters, 50(13), 1482-1484 (2009)
Asymmetric synthesis of γ-butyrolactones by enantioselective hydrogenation of butenolides
Donate PM, et al.
Tetrahedron Asymmetry, 14(20), 3253-3256 (2003)
Synthesis of stereoarray isotope labeled (SAIL) lysine via the ?Head-to-Tail? conversion of SAIL glutamic Acid
Terauchi T, et al.
Organic Letters, 13(1), 161-163 (2011)
An efficient chiral synthesis of fluoro-containing amino acids: N-benzyloxycarbonyl-2-amino-4, 4-difluorobutyric acid methyl ester and its analogs
Hu Z and Han W
Tetrahedron Letters, 49(5), 901-902 (2008)
商品
Asymmetric hydrogenation enables scalable synthesis of single-enantiomer compounds with minimal byproducts, ideal for commercial manufacturing.
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.
联系客户支持