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(S)-VAPOL hydrogenphosphate_Molecular_structure_CAS_871130-17-5)
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(S)-VAPOL hydrogenphosphate

Catalog No. 688320 Name Sigma Aldrich
CAS Number 871130-17-5 Website http://www.sigmaaldrich.com
M. F. C40H25O4P Telephone 1-800-521-8956
M. W. 600.597861 Fax
Purity Email
Storage Chembase ID: 140152

SYNONYMS

Title
(S)-VAPOL 磷酸氢酯
IUPAC name
17-hydroxy-3,31-diphenyl-16,18-dioxa-17λ5-phosphaheptacyclo[17.12.0.02,15.05,14.08,13.020,29.021,26]hentriaconta-1(31),2,4,6,8,10,12,14,19,21,23,25,27,29-tetradecaen-17-one
IUPAC Traditional name
17-hydroxy-3,31-diphenyl-16,18-dioxa-17λ5-phosphaheptacyclo[17.12.0.02,15.05,14.08,13.020,29.021,26]hentriaconta-1(31),2,4,6,8,10,12,14,19,21,23,25,27,29-tetradecaen-17-one
Synonyms
(S)-18-羟基-8,9-二苯基-联菲并[4,3-d:3′,4′-f][1,3,2]二噁磷杂庚英-18-氧化物
(S)-18-Hydroxy-8,9-diphenyl-diphenanthro[4,3-d:3′,4′-f][1,3,2]dioxaphosphepin-18-oxide
(S)-2,2′-Diphenyl-3,3′-biphenanthryl-4,4′-diyl phosphate
(S)-VAPOL phosphoric acid
(S)-VAPOL 磷酸
(S)-2,2′-二苯基-3,3′-联菲-4,4′-二基磷酸酯

DATABASE IDS

CAS Number 871130-17-5
MDL Number MFCD09265084

PROPERTIES

Empirical Formula (Hill Notation) C40H25O4P
Melting Point >400 °C
Optical Rotation [α]22/D +412°, c = 1 in chloroform
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
German water hazard class 3

DETAILS

Description (English)
Packaging
100, 500 mg in glass bottle
Application
Catalyst for:
• Benzoyloxylation of (aryl)oxindoles with benzoyl peroxide1
• Enantioselective synthesis of homoaldols and cyclic acetals via kinetic resoln of homoaldols2
• Desymmetrization of mono- and bicyclic N-acyl meso-aziridines by ring opening3,4
• Highly enantioselective addition of imides to imines to give aminals5
• Friedel-Crafts reaction of pyrroles with benzylidenebenzamides6
Description (简体中文)
包装
100, 500 mg in glass bottle
Application
Catalyst for:
• Benzoyloxylation of (aryl)oxindoles with benzoyl peroxide1
• Enantioselective synthesis of homoaldols and cyclic acetals via kinetic resoln of homoaldols2
• Desymmetrization of mono- and bicyclic N-acyl meso-aziridines by ring opening3,4
• Highly enantioselective addition of imides to imines to give aminals5
• Friedel-Crafts reaction of pyrroles with benzylidenebenzamides6

REFERENCES