![(S)-(+)-Benzyl(3,5-dioxa-4-phospha-cyclohepta[2,1-a;3,4-a′]dinaphthalen-4-yl)methylamine (CAS 490023-37-5) - chemical structu](https://media.scbt.com/product/s-benzyl3-5-dioxa-4-phospha-cyclohepta2-1-a3-4-aprimedinaphthalen-4-ylmethylamine-490023-37-5-structure_11_27_b_112724.jpg)
![(S)-(+)-Benzyl(3,5-dioxa-4-phospha-cyclohepta[2,1-a;3,4-a′]dinaphthalen-4-yl)methylamine (CAS 490023-37-5) - chemical structu](https://media.scbt.com/product/s-benzyl3-5-dioxa-4-phospha-cyclohepta2-1-a3-4-aprimedinaphthalen-4-ylmethylamine-490023-37-5-structure_11_27_t_112724.jpg "Molecular structure of (S)-(+)-Benzyl(3,5-dioxa-4-phospha-cyclohepta[2,1-a;3,4-a′]dinaphthalen-4-yl)methylamine, CAS Number: 490023-37-5")
Molecular structure of (S)-(+)-Benzyl(3,5-dioxa-4-phospha-cyclohepta[2,1-a;3,4-a′]dinaphthalen-4-yl)methylamine, CAS Number: 490023-37-5
(S)-(+)-Benzyl(3,5-dioxa-4-phospha-cyclohepta[2,1-a;3,4-a′]dinaphthalen-4-yl)methylamine (CAS 490023-37-5)
CAS Number:
490023-37-5
Molecular Weight:
435.45
Molecular Formula:
C28H22NO2P
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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Phosphoramidite ligand used in a rhodium-catalyzed enantioselective 1,4-addition of arylboronic acids to α,-unsaturated carbonyl compounds.(1) Also used in asymmetric hydrogenation of N-acylated -dehydroamino esters to enantiopure -amino acid derivatives.(2)
(S)-(+)-Benzyl(3,5-dioxa-4-phospha-cyclohepta[2,1-a;3,4-a′]dinaphthalen-4-yl)methylamine (CAS 490023-37-5) References
1. J. Organomet. Chem. 692, 428, (2007) 2. J. Am. Chem. Soc. 124, 14552, (2002)Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
(S)-(+)-Benzyl(3,5-dioxa-4-phospha-cyclohepta[2,1-a;3,4-a′]dinaphthalen-4-yl)methylamine, 100 mg | sc-253097 | 100 mg | $63.00 | |||
(S)-(+)-Benzyl(3,5-dioxa-4-phospha-cyclohepta[2,1-a;3,4-a′]dinaphthalen-4-yl)methylamine, 500 mg | sc-253097A | 500 mg | $249.00 |