Other Aliphatic Heterocycles ∩ Amides-Other Aliphatic Heterocycles| Ambeed

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Chemistry Organic Building Blocks Phosphoruses Phosphoruses ∩ Aliphatic Chain Hydrocarbons

Phosphoruses ∩ Aliphatic Chain Hydrocarbons

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Purity

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99+%
99%
98+%
98%
97+%
97%
96+%
96%
95+%
95%
93%
90+%
90%

Size

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1mg
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5mg
10mg
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1g
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Conditions to empty

Framework+−

1,1,1-trifluoro-N-(4-oxido-2,6-diphenyldinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl)methanesulfonamide diethyl benzylphosphonate dimethyl(phenyl)phosphine oxide ethyltriphenylphosphonium methyltriphenylphosphonium phenyl phosphate phenylphosphonic acid

By Key Group+−

di-tert-butylphosphine diethoxyphosphoryl diethyl methy phosphonate dihydrogen phosphate dihydrogentriphosphate diisopropylphosphoramidite dimethoxyphosphoryl dimethoxyphosphoryl dimethylphosphine dimethylphosphoryl dioxaphosphepine diphosphate diphosphonic diyldiphosphonic diyldiphosphonic phosphonic acid phosphoramidite phosphorothioate trifluoromethyl-phenyl-phosphino triphenylphosphine

By Parent Nucleus+−

Aliphatic Heterocycles Aromatic Heterocycles Furans Imidazoles Indazoles Other Aliphatic Heterocycles Other Aromatic Heterocycles Piperidines Purines Pyrazoles Pyridines Pyrimidines Pyrrolidines Tetrahydropyrans

By Functional Group+−

Alcohols Aliphatic Chain Hydrocarbons Aliphatic Cyclic Hydrocarbons Alkynyls Amides Amines Aryls Bromides Carboxylic Acids Chiral Building Blocks Chlorides Esters Ethers Fluorinated Building Blocks Ketones Nitriles Nitroes Oximes Phenols Sulfonates Sulfonic Acids Trifluoromethyls

Phosphorus related+−

P

By Chemical Elements+−

CClOPPd CP CClFNP CFNPRu CNP CClNiP CFeP COP CNaOP CClPPd CClPRh CClNP CNOP CNNaOP CFOP CO CFNOP CFNOPS CNOPS CGdNOP.Na CBP CFNP CClFePPd CClOP CBFNOP CNOPPdS CClNOP CNOS COPS CNOP.xO CBNP CBrFNP CBrNP CCaOP CNaOP.xO CPPd COPPd

B^x

C^x

N^x

O^x

F^x

Si^x

P^x

S^x

Cl^x

Br^x

I^x

Formula Weight+−

0-100(1) 100-200(6) 200-300(35) 300-400(51) 400-500(50) 500-600(43) 600-700(21) 700-800(23) 800-900(9) 900-1000(14) 1000+(3)

cLogP+−

(-50,-10] (-10,-5] (-5,-3] (-3,-2] (-2,-1] (-1,0] (0,0.5] (0.5,1] (1,1.5] (1.5,2] (2,2.5] (2.5,3] (3,3.5] (3.5,4] (4,4.5] (4.5,5] (5,5.5] (5.5,6] (6,10] (10,50]

H-Acceptors+−

0 1 2 3 4 5 6 7 9 8 10 (10,20] (20,200]

H-Donors+−

0 1 2 3 4 5 6 7 9 8 10 (10,20] (20,200]

Polar Surface Area+−

[0,10] (10,20] (20,30] (30,40] (40,50] (50,60] (60,70] (70,80] (80,90] (90,100] ＞100

Druglikeness+−

≤-20 [-20,-10] (-10,-6] (-6,-3] (-3,-1] (-1,0] (0,1] (1,2] (2,5] (5,20]

N_NCH/N_NH+−

[0,0.05] (0.05,0.1] (0.1,0.15] (0.15,0.2] (0.2,0.25] (0.25,0.3] (0.3,0.35] (0.35,0.4] (0.4,0.45] (0.45,0.5] (0.5,0.55] (0.55,0.6] (0.6,1]

sp3-Atoms+−

0 1 2 3 4 5 6 7 8 9 10 (10,20] (20,30] ＞30

Non-Aromatic Rings+−

0 1 2 3 [4,6] [7,10] ＞10

Aromatic Rings+−

0 1 2 3 [4,6] [7,10] ＞10

Rotatable Bonds+−

0 1 2 3 4 5 6 7 8 9 10 (10,20] ＞20

By Configuration+−

RS configuration

No Data

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