(S)-VAPOL HYDROGENPHOSPHATE - CAS 871130-17-5

(S)-VAPOL HYDROGENPHOSPHATE is a chiral phosphoric acid catalyst for a variety of enantioselective transformations, especially for carbon-carbon and carbon-heteroatom bond-forming reactions.

Product Information

Canonical SMILES
OP1(OC2=C3C4=CC=CC=C4C=CC3=CC(C5=CC=CC=C5)=[C@@]2[C@@]6=C(C7=CC=CC=C7)C=C8C=CC9=CC=CC=C9C8=C6O1)=O
InChI
InChI=1S/C40H25O4P/c41-45(42)43-39-35-29(21-19-27-15-7-9-17-31(27)35)23-33(25-11-3-1-4-12-25)37(39)38-34(26-13-5-2-6-14-26)24-30-22-20-28-16-8-10-18-32(28)36(30)40(38)44-45/h1-24H,(H,41,42)
InChI Key
YKIJNEDTUDPMNC-UHFFFAOYSA-N
Purity
95%
MDL
MFCD09265084
Appearance
White to tan solid
Storage
Inert atmosphere. Keep cold.
Melting Point
>400°C
Optical Activity
+412°( c = 1 in chloroform)
WGK Germany
3

Safety Information

Signal Word
Warning
Precautionary Statement
P261 - P280 - P301 - P312 - P302 - P352 - P305 - P351 - P338
Hazard Statements
H302 - H315 - H319 - H335

Reference Reading

1.Amorphous iron-(hydr) oxide networks at liquid/vapor interfaces: in situ X-ray scattering and spectroscopy studies.
Wang W1, Pleasants J, Bu W, Park RY, Kuzmenko I, Vaknin D. J Colloid Interface Sci. 2012 Oct 15;384(1):45-54. doi: 10.1016/j.jcis.2012.06.024. Epub 2012 Jun 23.
Surface sensitive X-ray reflectivity (XR), fluorescence (XF), and grazing incidence X-ray diffraction (GIXD) experiments were conducted to determine the accumulation of ferric iron Fe (III) or ferrous iron Fe (II) under dihexadecyl phosphate (DHDP) or arachidic acid (AA) Langmuir monolayers at liquid/vapor interfaces. Analysis of the X-ray reflectivity and fluorescence data of monolayers on the aqueous subphases containing FeCl(3) indicates remarkably high levels of surface-bound Fe (III) in number of Fe(3+) ions per molecule (DHDP or AA) that exceed the amount necessary to neutralize a hypothetically completely deprotonated monolayer (DHDP or AA). These results suggest that nano-scale iron (hydr) oxide complexes (oxides, hydroxides or oxyhydroxides) bind to the headgroups and effectively overcompensate the maximum possible charges at the interface. The lack of evidence of in-plane ordering in GIXD measurements and strong effects on the surface-pressure versus molecular area isotherms indicate that an amorphous network of iron (hydr) oxide complexes contiguous to the headgroups is formed.
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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