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关于此项目
经验公式(希尔记法):
C25H19N3O2
化学文摘社编号:
分子量:
393.44
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352005
MDL number:
Quality Level
assay
≥94%
form
solid
optical activity
[α]20/D +386°, c = 1 in methylene chloride(lit.)
mp
284 °C (dec.)
functional group
ether
SMILES string
C1[C@@H]2OC(=N[C@@H]2c3ccccc13)c4cccc(n4)C5=N[C@H]6[C@H](Cc7ccccc67)O5
InChI
1S/C25H19N3O2/c1-3-8-16-14(6-1)12-20-22(16)27-24(29-20)18-10-5-11-19(26-18)25-28-23-17-9-4-2-7-15(17)13-21(23)30-25/h1-11,20-23H,12-13H2/t20-,21-,22+,23+/m0/s1
InChI key
BZSJUFJXCHHRHW-MYDTUXCISA-N
Application
Catalytic ligand used for:
- [3+2] cycloaddition of N-tosyl aziridines with electron-rich alkenes via selective carbon-carbon bond cleavage
- Enantioselective Mukaiyama-aldol reactions
- Enantioselective carbonyl-ene reactions
- Cu(I)-catalyzed asymmetric alkynylation of imino esters with terminal alkynes
- Asymmetric three-component coupling reactions catalyzed by a Cu/pybox complex
- Enantioselective Diels-Alder reaction
- Ni-catalyzed cross-coupling reactions
hcodes
Hazard Classifications
Aquatic Chronic 4
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
商品
The PYBOX ligand, consisting of a pyridine ring flanked by two oxazoline groups, was introduced in 1989 by Nishiyama.
PYBOX配体由吡啶环侧接两个恶唑啉基团组成,由Nishiyama在1989年合成成功。
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 673986-250MG | 04061832986999 |
| 673986-1G | 04061826263235 |