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[PDF] Top 20 3,5 Di­methyl 2,6 di­phenyl­piperidine

Has 10000 "3,5 Di­methyl 2,6 di­phenyl­piperidine" found on our website. Below are the top 20 most common "3,5 Di­methyl 2,6 di­phenyl­piperidine".

{2,6 Bis[(di tert butyl­phosphino)­methyl]­phenyl}chloridonickel(II)

{2,6 Bis[(di tert butyl­phosphino)­methyl]­phenyl}chloridonickel(II)

... Ni1 0.02964 (9) 0.02516 (9) 0.02389 (9) −0.00470 (8) −0.00320 (8) 0.00305 (7) Cl1 0.0605 (3) 0.0569 (3) 0.02997 (19) −0.0283 (3) −0.00855 (19) 0.0151 (2) P1 0.02591 (18) 0.02588 (17) 0.02911 ... See full document

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Synthesis and antifungal activity 2, 6 bis (subtituted phenyl) 1, 4 dihydro 3, 5  di (1H imidazol 1 yl) 4 (subtituted phenyl) pyridine derivatives

Synthesis and antifungal activity 2, 6 bis (subtituted phenyl) 1, 4 dihydro 3, 5 di (1H imidazol 1 yl) 4 (subtituted phenyl) pyridine derivatives

... The final derivatives (4a-4p) were evaluated for their antifungal activity against (Table 2) representative strains of yeasts: Candida albicans ATCC 100231 (C. albicans),: Aspergillus flavus NCL 535/NRRL 2211 (A. ... See full document

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Ethyl 2 {[(1Z) (3 methyl 5 oxo 1 phenyl 1,5 di­hydro­pyrazol 4 yl­­idene)(phenyl)­methyl]­amino} 3 phenyl­propanoate

Ethyl 2 {[(1Z) (3 methyl 5 oxo 1 phenyl 1,5 di­hydro­pyrazol 4 yl­­idene)(phenyl)­methyl]­amino} 3 phenyl­propanoate

... In recent years, the Schiff bases derived from 4-acyl-5-pyra- zolones and their metal complexes have been studied widely for their high antibacterial activation (Li et al., 1997, 2004). Since amino acid esters ... See full document

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5′′ (2 Fluoro­benzyl­­idene) 1′ (2 fluoro­phen­yl) 1′′ methyl 1′,2′,3′,5′,6′,7′,8′,8a' octa­hydro­di­spiro­[ace­naphthyl­ene 1,3′ indolizine 2′,3′′ piperidine] 2,4′′(1H) dione

5′′ (2 Fluoro­benzyl­­idene) 1′ (2 fluoro­phen­yl) 1′′ methyl 1′,2′,3′,5′,6′,7′,8′,8a' octa­hydro­di­spiro­[ace­naphthyl­ene 1,3′ indolizine 2′,3′′ piperidine] 2,4′′(1H) dione

... C34 0.096 (2) 0.087 (2) 0.0681 (18) 0.0404 (17) 0.0198 (16) −0.0181 (15) C33 0.0709 (16) 0.0585 (15) 0.0510 (13) 0.0196 (12) 0.0096 (12) −0.0076 (11) C71 0.0424 (10) 0.0361 (10) 0.0395 (10) 0.0038 (8) ... See full document

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2,4 Di tert butyl 6 [1 (3,5 di tert butyl 2 hy­droxy­phen­yl)eth­yl]phenyl 4 methyl­benzene­sulfonate

2,4 Di tert butyl 6 [1 (3,5 di tert butyl 2 hy­droxy­phen­yl)eth­yl]phenyl 4 methyl­benzene­sulfonate

... C26′ 0.094 (7) 0.170 (11) 0.22 (2) 0.069 (8) 0.100 (11) 0.106 (14) C27′ 0.109 (7) 0.101 (6) 0.141 (10) −0.029 (5) 0.095 (7) −0.023 (5) C28 0.0802 (16) 0.0712 (16) 0.0409 (12) 0.0019 (12) ... See full document

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EVALUATION OF SUBSTITUTED PYRIMIDINE HYBRIDS FOR ANTIBACTERIAL AND ANTI FUNGAL ACTIVITY: FACILE SYNTHESES UNDER CATALYSIS BY IONIC LIQUID

EVALUATION OF SUBSTITUTED PYRIMIDINE HYBRIDS FOR ANTIBACTERIAL AND ANTI FUNGAL ACTIVITY: FACILE SYNTHESES UNDER CATALYSIS BY IONIC LIQUID

... The present method for the synthesis of substituted 1-(1-(6-methyl-2-oxo-4-phenyl-1,2,3,4- tetrahydropyrimidin-5-yl)ethylidene)thiosemicarbazide (2a-i) has many obvious advantages over ... See full document

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5 Chloro 4 [(2 chloro­benzoyl­hydrazono)methyl] 3 methyl 1 phenyl 1H pyrazole

5 Chloro 4 [(2 chloro­benzoyl­hydrazono)methyl] 3 methyl 1 phenyl 1H pyrazole

... Cl1 0.0986 (5) 0.0762 (4) 0.1374 (7) −0.0006 (3) 0.0717 (5) 0.0358 (4) Cl2 0.0377 (3) 0.0675 (3) 0.0724 (4) −0.0124 (2) 0.0240 (2) −0.0226 (2) O1 0.0391 (7) 0.0716 ... See full document

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1′ Methyl 5′ phenyl 2′',3′',5′',6′′ tetra­hydro­indoline 3 spiro 3′ pyrrolidine 4′ spiro 2′' imidazo­[2,1 b]­thia­zole 2,3′' dione

1′ Methyl 5′ phenyl 2′',3′',5′',6′′ tetra­hydro­indoline 3 spiro 3′ pyrrolidine 4′ spiro 2′' imidazo­[2,1 b]­thia­zole 2,3′' dione

... + 2]-cycloaddition of azomethine ylide, derived from isatin and sarcosine by a decarboxylative route, and ...planar 2-oxoindoline ring, a pyrrolidine ring in an envelope conformation, and a ... See full document

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2 (Di phenyl methyl idene) 2,3 di hydro 1H inden 1 one

2 (Di phenyl methyl idene) 2,3 di hydro 1H inden 1 one

... with the dihedral angles 70.30 (12)° and 44.74 (13)°, respectively. The torsion angles of these two benzene groups are [C14—C7—C8—C9] = 56.4 (3)° and [C14—C7—C6—C5] = 36.5 (4)°. The rest of the molecule is ... See full document

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Methyl 3 di­methyl­amino 2 {2 [2 (di­methyl­amino) 1 (3 phenyl 1,2,4 oxa­diazol 5 yl)­vinyl­­oxy]­phenyl}acryl­ate

Methyl 3 di­methyl­amino 2 {2 [2 (di­methyl­amino) 1 (3 phenyl 1,2,4 oxa­diazol 5 yl)­vinyl­­oxy]­phenyl}acryl­ate

... C50 0.096 (4) 0.112 (5) 0.113 (5) 0.000 (4) −0.044 (4) −0.033 (4) C51 0.098 (4) 0.070 (3) 0.084 (4) −0.013 (3) −0.024 (3) −0.024 (3) C52 0.052 (3) 0.052 (2) 0.058 ... See full document

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Ethyl 6 methyl 2 (3 nitro­phen­­oxy) 4 oxo 3 phenyl 3,4 di­hydro­furo[2,3 d]pyrimidine 5 carboxyl­ate

Ethyl 6 methyl 2 (3 nitro­phen­­oxy) 4 oxo 3 phenyl 3,4 di­hydro­furo[2,3 d]pyrimidine 5 carboxyl­ate

... To a solution of N-(3,4-diethoxycarbonyl-5-methylfuran-2-yl)imino- triphenylphosphorane (3 mmol) in dry dichloromethane (15 ml) was added phenyl isocyanate (3 mmol) under nitrogen at ... See full document

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Methyl 6 meth­oxy­carbonyl­methyl 2 oxo 4 phenyl 1,2,3,4 tetra­hydro­pyrimidine 5 carboxyl­ate

Methyl 6 meth­oxy­carbonyl­methyl 2 oxo 4 phenyl 1,2,3,4 tetra­hydro­pyrimidine 5 carboxyl­ate

... N1 0.0531 (6) 0.0410 (5) 0.0532 (6) −0.0021 (5) −0.0084 (5) 0.0027 (5) C2 0.0392 (6) 0.0429 (7) 0.0574 (8) −0.0001 (6) −0.0032 (6) 0.0048 (6) O1 ... See full document

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Ethyl 6 methyl 2 oxo 4 phenyl 1,2,3,4 tetra­hydro­pyrimidine 5 carboxyl­ate

Ethyl 6 methyl 2 oxo 4 phenyl 1,2,3,4 tetra­hydro­pyrimidine 5 carboxyl­ate

... O1 0.0364 (4) 0.0620 (5) 0.0619 (5) 0.0227 (4) 0.0271 (4) 0.0348 (5) O2 0.0412 (5) 0.0638 (6) 0.0791 (7) 0.0260 (4) 0.0348 (5) 0.0359 (5) O3 0.0454 (5) 0.0496 ... See full document

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5 Iodo 7 methyl 3 methyl­sulfinyl 2 phenyl 1 benzo­furan

5 Iodo 7 methyl 3 methyl­sulfinyl 2 phenyl 1 benzo­furan

... benzofuran fragment, with the O atom and the methyl group of the methylsulfinyl substituent lying on opposite sides of this plane. The crystal structure exhibits intermolecular C—H I interactions, and an I O ... See full document

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Synthesis of lanthanon complexes with βββdiketones and study of their spectral and electrochemical behavior

Synthesis of lanthanon complexes with βββdiketones and study of their spectral and electrochemical behavior

... − Phenyl3methyl pyrazolone − 5, acetyl chloride, 95% ethanol, dioxane and petroleum ether (40 − 60 ° ...− Phenyl3Methyl − 4 − Acetoxime Pyrazolone − ... See full document

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Ethyl 3 methyl 6 oxo 5 [3 (tri­fluoro­methyl)­phenyl] 1,6 di­hydro 1 pyridazine­acetate

Ethyl 3 methyl 6 oxo 5 [3 (tri­fluoro­methyl)­phenyl] 1,6 di­hydro 1 pyridazine­acetate

... C15′ 0.104 (10) 0.128 (14) 0.089 (13) −0.035 (9) 0.008 (8) 0.034 (9) C16′ 0.126 (10) 0.084 (9) 0.148 (16) −0.008 (8) −0.007 (12) 0.055 (10) F3" 0.167 (6) 0.106 (6) 0.086 (4) −0.021 (5) 0.017 ... See full document

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2,4 Di(butyl­ureido) 6 methyl s triazine

2,4 Di(butyl­ureido) 6 methyl s triazine

... ethanol/water 2:1 v/v. Column chromatography (6% THF in chloro- form), followed by crystallization from ethyl acetate and treatment with active carbon, gave an analytically pure sample ... See full document

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3,3,4,4,5,5 Hexa­fluoro 1 [5 (3 fluoro­phen­yl) 2 methyl 3 thien­yl] 2 (2 methyl 5 phenyl 3 thien­yl)cyclo­pent 1 ene

3,3,4,4,5,5 Hexa­fluoro 1 [5 (3 fluoro­phen­yl) 2 methyl 3 thien­yl] 2 (2 methyl 5 phenyl 3 thien­yl)cyclo­pent 1 ene

... hexafluorocyclopentene rings of the two molecules, the C1═C2 and C28═C29 bonds are clearly double bonds, while the other bonds in the ring are single. The thiophene rings are linked by the C1═C2 and C28═C29 double bonds; ... See full document

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5 Methyl 2 phenyl 2H pyrazol 3 ol

5 Methyl 2 phenyl 2H pyrazol 3 ol

... C9 0.0599 (9) 0.0477 (9) 0.0523 (8) 0.0013 (7) −0.0006 (7) 0.0069 (7) C10 0.0886 (13) 0.0739 (12) 0.0622 (10) −0.0045 (10) −0.0120 (9) −0.0032 (9) C11 0.0544 (8) 0.0339 (7) 0.0447 (7) 0.0122 (6) 0.0093 (6) ... See full document

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Methyl 6 amino 5 cyano 2 meth­oxy­carbonyl­methyl 4 phenyl 4H pyran 3 carboxyl­ate

Methyl 6 amino 5 cyano 2 meth­oxy­carbonyl­methyl 4 phenyl 4H pyran 3 carboxyl­ate

... O1 0.0351 (5) 0.0316 (5) 0.0559 (6) −0.0019 (4) −0.0016 (4) −0.0100 (4) O2 0.0395 (6) 0.0531 (7) 0.0992 (10) −0.0033 (5) −0.0083 (6) −0.0295 (7) O3 0.0497 (6) 0.0382 ... See full document

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