2-(Diphenylphosphino)ethylamine
Product Information
Molecular Formula
C14H16NP
Molecular Weight
229.26
Description
2-(Diphenylphosphino)ethylamine is a chiral phosphine ligand for enantioselective synthesis with high yield and high enantioselective results.
Synonyms
2-(DIPHENYLPHOSPHINO)ETHYLAMINE; 2-(DIPHENYLPHOSPHINO)ETHANAMINE; (2-AMINOETHYL)DIPHENYLPHOSPHINE; 2-(Diphenylphosphino)ethylamine,min.94%; 2-(Diphenylphosphino)ethylamine ,95%; 2-(Diphenylphosphino)ethylamine, min. 94%
IUPAC Name
2-diphenylphosphanylethanamine
SMILES
C1=CC=C(C=C1)P(CCN)C2=CC=CC=C2
InChI
InChI=1S/C14H16NP/c15-11-12-16(13-7-3-1-4-8-13)14-9-5-2-6-10-14/h1-10H,11-12,15H2
InChI Key
RXEPBCWNHKZECN-UHFFFAOYSA-N
Boiling Point
341.1°Cat 760 mmHg
Flash Point
Not applicable
Purity
95%
Appearance
colorless or light yellow liquid
Safety Information
Hazards
H314
Precautionary Statement
P280 - P305 + P351 + P338 - P310
Signal Word
Danger
Computed Properties
XLogP3
2.1
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
4
Exact Mass
229.102036512 g/mol
Monoisotopic Mass
229.102036512 g/mol
Topological Polar Surface Area
26Ų
Heavy Atom Count
16
Formal Charge
0
Complexity
165
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| CN-113943322-A | Azepilazphosphine ligand and preparation method and application thereof | 2021-10-12 |
| CN-114133275-A | Fiber chelating type monoammonium phosphate and preparation method thereof | 2021-09-08 |
| CN-112830449-A | Reversible liquid organic hydrogen storage method based on manganese catalytic hydrogenation and dehydrogenation reaction | 2019-11-22 |
| CN-110590658-A | Method for catalytic hydrogenation of nitrogen-containing unsaturated heterocyclic compound | 2019-10-11 |
| CN-110590658-B | Method for catalytic hydrogenation of nitrogen-containing unsaturated heterocyclic compound | 2019-10-11 |
| WO-2021001240-A1 | Hydrogenation of esters to alcohols in the presence of a ru-pnn complex | 2019-07-03 |
| CN-114080379-A | Hydrogenation of esters to alcohols in the presence of Ru-PNN complexes | 2019-07-03 |
| US-2020405874-A1 | Methods of preparing cell-binding agent-drug conjugates | 2019-03-21 |
| WO-2020191306-A1 | Methods of preparing cell-binding agent-drug conjugates | 2019-03-21 |
| TW-202102270-A | Methods of preparing cell-binding agent-drug conjugates | 2019-03-21 |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 22090896 | 2011-08-01 | (Acetonitrile-κN)[2-(diphenylphosphan-yl)ethanamine-κN,P][(1,2,3,4,5-η)-1,2,3,4,5-pentamethylcyclopentadienyl]iron(II) hexafluoridophosphate tetrahydrofuran monosolvate | Acta crystallographica. Section E, Structure reports online |
| 20028110 | 2010-02-01 | Template synthesis of iron(II) complexes containing tridentate P-N-S, P-N-P, P-N-N, and tetradentate P-N-N-P ligands | Inorganic chemistry |
