isopropyl p-nitrophenyl methylphosphonate; R(-)enantiomer

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Properties

MW HBA HBD LogP TPSA Rot. Comp. Fsp3C Brutto formula
None None None None None

Availability

Suppliers Supplier IDs Storage Storage ID Quantity Class Added
JN_293 None Jan. 1, 2023

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PAINS

Identified PAINS

Supramolecules

Namelog KSDpHT(°C)MethodRef
[a-Cyclodextrin](1).[isopropyl p-nitrophenyl methylphosphonate; R(-)enantiomer] -0.40 -1.49 12.0 25.0 spectrophotometry C.van Hooidonk 1970
[a-Cyclodextrin](1).[isopropyl p-nitrophenyl methylphosphonate; R(-)enantiomer] -0.46 -1.32 12.3 25.0 spectrophotometry C.van Hooidonk 1970
[a-Cyclodextrin](1).[isopropyl p-nitrophenyl methylphosphonate; R(-)enantiomer] -0.51 -1.11 12.6 25.0 spectrophotometry C.van Hooidonk 1970
[a-Cyclodextrin](1).[isopropyl p-nitrophenyl methylphosphonate; R(-)enantiomer] -0.54 -1.61 12.8 25.0 spectrophotometry C.van Hooidonk 1970
[a-Cyclodextrin](1).[isopropyl p-nitrophenyl methylphosphonate; R(-)enantiomer] -0.59 -0.86 12.9 25.0 spectrophotometry C.van Hooidonk 1970
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