(S)-VAPOL phosphoric acid, (S)-2,2μ-Diphenyl-3,3μ-biphenanthryl-4,4μ-diyl phosphate, (S)-18-Hydroxy-8,9-diphenyl-diphenanthro[4,3-d:3μ,4μ-f][1,3,2]dioxaphosphepin-18-oxide
(S)-VAPOL phosphoric acid, (S)-2,2μ-Diphenyl-3,3μ-biphenanthryl-4,4μ-diyl phosphate, (S)-18-Hydroxy-8,9-diphenyl-diphenanthro[4,3-d:3μ,4μ-f][1,3,2]dioxaphosphepin-18-oxide Basic information
- Product Name:
- (S)-VAPOL phosphoric acid, (S)-2,2μ-Diphenyl-3,3μ-biphenanthryl-4,4μ-diyl phosphate, (S)-18-Hydroxy-8,9-diphenyl-diphenanthro[4,3-d:3μ,4μ-f][1,3,2]dioxaphosphepin-18-oxide
- Synonyms:
-
- (S)-VAPOL hydrogenphosphate
- (S)-VAPOL phosphoric acid, (S)-2,2μ-Diphenyl-3,3μ-biphenanthryl-4,4μ-diyl phosphate, (S)-18-Hydroxy-8,9-diphenyl-diphenanthro[4,3-d:3μ,4μ-f][1,3,2]dioxaphosphepin-18-oxide
- 8,9-Diphenyldiphenanthro[4,3-d:3',4'-f][1,3,2]dioxaphosphepin-18-ol 18-oxide
- (S)-VAPOL Hydrogen Phosphate,99%e.e.
- (8aS)-18-Hydroxy-8,9-diphenyl-18-oxide-diphenanthro[4,3-d:3',4'-f][1,3,2]dioxaphosphepin
- (S)-VAPOL phosphoric acid, (S)-2,2μ-Diphenyl-3,3μ-biphenanthryl-4,4μ-diyl phosphate, (S)-18-Hydroxy-8,9-diphenyl-diphenanthro[4,3-d
- 3μ,4μ-f][1,3,2]dioxaphosphepin-18-oxide
- Diphenanthro[4,3-d:3',4'-f][1,3,2]dioxaphosphepin, 18-hydroxy-8,9-diphenyl-, 18-oxide, (8aS)-
- CAS:
- 871130-17-5
- MF:
- C40H25O4P
- MW:
- 600.6
- Mol File:
- 871130-17-5.mol
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(S)-VAPOL phosphoric acid, (S)-2,2μ-Diphenyl-3,3μ-biphenanthryl-4,4μ-diyl phosphate, (S)-18-Hydroxy-8,9-diphenyl-diphenanthro[4,3-d:3μ,4μ-f][1,3,2]dioxaphosphepin-18-oxide Chemical Properties
- Melting point:
- >400 °C
- Density
- 1.44±0.1 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- pka
- 1.13±0.20(Predicted)
- optical activity
- [α]22/D +412°, c = 1 in chloroform
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(S)-VAPOL phosphoric acid, (S)-2,2μ-Diphenyl-3,3μ-biphenanthryl-4,4μ-diyl phosphate, (S)-18-Hydroxy-8,9-diphenyl-diphenanthro[4,3-d:3μ,4μ-f][1,3,2]dioxaphosphepin-18-oxide Usage And Synthesis
Uses
Catalyst for:
- Benzoyloxylation of (aryl)oxindoles with benzoyl peroxide
- Enantioselective synthesis of homoaldols and cyclic acetals via kinetic resoln of homoaldols
- Desymmetrization of mono- and bicyclic N-acyl meso-aziridines by ring opening
- Highly enantioselective addition of imides to imines to give aminals
- Friedel-Crafts reaction of pyrroles with benzylidenebenzamides
(S)-VAPOL phosphoric acid, (S)-2,2μ-Diphenyl-3,3μ-biphenanthryl-4,4μ-diyl phosphate, (S)-18-Hydroxy-8,9-diphenyl-diphenanthro[4,3-d:3μ,4μ-f][1,3,2]dioxaphosphepin-18-oxideSupplier
Daicel Chiral Technologies (China)CO.,LTD
- Tel
- 021-50460086-9 15921403865
- han_yajun@dctc.daicel.com
Bide Pharmatech Ltd.
- Tel
- 400-1647117 15221909166
- product02@bidepharm.com
Sigma-Aldrich
- Tel
- 021-61415566 800-8193336
- orderCN@merckgroup.com
Shanghai Chiral bio-compound co., Ltd.
- Tel
- 021-5068 3667/17749785980/1029026415; 17749785980
- 1029026415@qq.com
LaaJoo
- Tel
- 021-60702684 18516024827
- huang.jiayi@sinocompound.com