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Quality Segment
assay
96%
form
solid
optical activity
[α]/D -34±4°, c = 1 in chloroform
mp
222-226 °C
functional group
phosphine
SMILES string
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
Application
- 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.
Legal Information
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Dieser Artikel | |||
|---|---|---|---|
| description 96% | description 97% | description - | description ≥95.0% (HPLC) |
| assay 96% | assay 97% | assay - | assay ≥95.0% (HPLC) |
| functional group phosphine | functional group phosphine | functional group - | functional group - |
| form solid | form solid | form solid | form solid |
| Quality Level 100 | Quality Level 100 | Quality Level 100 | Quality Level - |
| mp 222-226 °C | mp 261-265 °C | mp - | mp - |
| optical activity [α]/D -34±4°, c = 1 in chloroform | optical activity [α]20/D +98°, c = 1 in chloroform | optical activity - | optical activity [α]/D 17±2°, c = 1 in H2O |
Lagerklasse
11 - Combustible Solids
Was ist los?
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
PSA (Persönliche Schutzausrüstung)
dust mask type N95 (US), Eyeshields, Gloves
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