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[PDF] Top 20 4 Acetyl 1H pyrrole 2 carbaldehyde

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4 Acetyl 1H pyrrole 2 carbaldehyde

4 Acetyl 1H pyrrole 2 carbaldehyde

... Some pyrrole derivatives which belong to this category exhibit interesting biological properties, such as anti-bacterial, anti-inflammatory, anti-oxidant, anti-tumor, anti- fungal, and immune suppressant ...NO ... See full document

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(+) cis 1 Acetyl 4 (4 {[(2R,4S) 2 (2,4 di­chloro­phenyl) 2 (1H imidazol 1 ylmeth­yl) 1,3 dioxolan 4 yl]­meth­oxy}phenyl)­piperazine [(2R,4S) (+) ketoconazole]

(+) cis 1 Acetyl 4 (4 {[(2R,4S) 2 (2,4 di­chloro­phenyl) 2 (1H imidazol 1 ylmeth­yl) 1,3 dioxolan 4 yl]­meth­oxy}phenyl)­piperazine [(2R,4S) (+) ketoconazole]

... C72 0.052 (1) 0.041 (1) 0.038 (1) −0.013 (1) −0.018 (1) −0.003 (1) C73 0.050 (1) 0.045 (2) 0.044 (1) −0.019 (1) −0.010 (1) −0.006 (1) C74 0.038 (1) 0.046 (1) 0.040 (1) −0.011 (1) −0.0086 (9) −0.008 (1) C75 0.043 ... See full document

17

4 Methyl 5 (4 nitro­benzyl­­idene) 2 oxo 2,5 di­hydro 1H pyrrole 3 carbo­nitrile

4 Methyl 5 (4 nitro­benzyl­­idene) 2 oxo 2,5 di­hydro 1H pyrrole 3 carbo­nitrile

... As a part of our efforts to develop donor-π-acceptor molecules for non-linear optical devices, we have synthesized the title compound in which the oxopyrrole nitrile analogue acts as donor and the nitro group is the ... See full document

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Ethyl 1,4 bis­­(4 chloro­phen­yl) 2 methyl 1H pyrrole 3 carboxyl­ate

Ethyl 1,4 bis­­(4 chloro­phen­yl) 2 methyl 1H pyrrole 3 carboxyl­ate

... the pyrrole ring (N1/C2/C3/C4/C5) with phenyl rings (C19/C20/C21/C22/C23/C24) and (C12/C13/C14/C15/C16/C17) are ...the pyrrole moiety, as indicated by the dihedral angle value of ... See full document

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Crystal structure of 4 (2 azido­phen­yl) 5 benzoyl 2 (1H indol 3 yl) 1H pyrrole 3 carbo­nitrile

Crystal structure of 4 (2 azido­phen­yl) 5 benzoyl 2 (1H indol 3 yl) 1H pyrrole 3 carbo­nitrile

... C21′ 0.055 (3) 0.040 (3) 0.053 (4) 0.002 (2) 0.028 (3) 0.016 (3) C22′ 0.077 (3) 0.069 (4) 0.070 (4) −0.005 (3) 0.014 (3) 0.027 (3) C23′ 0.115 (4) 0.072 (4) 0.108 (5) 0.005 (3) ... See full document

10

Methyl 4 (tri­fluoro­meth­yl) 1H pyrrole 3 carboxyl­ate

Methyl 4 (tri­fluoro­meth­yl) 1H pyrrole 3 carboxyl­ate

... Sodium hydride (0.02 mol) and methyl 4,4,4-trifluorobut-2-enoate (0.01 mol) were taken in dry Tetrahydrofuran (THF). The reaction mixture was stirred for 15 min. Toluenesulfonylmethyl isocyanide (TosMIC, 0.01 mol) ... See full document

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3 (4 Bromo­phen­yl) 1 phenyl 1H pyrazole 4 carbaldehyde

3 (4 Bromo­phen­yl) 1 phenyl 1H pyrazole 4 carbaldehyde

... C12 0.053 (3) 0.062 (2) 0.052 (2) 0.003 (2) 0.0122 (19) 0.028 (2) O13 0.0653 (19) 0.0557 (16) 0.075 (2) −0.0154 (14) 0.0153 (16) 0.0234 (15) C14 0.034 (2) 0.060 (2) 0.043 ... See full document

9

5 Acetyl 4 (4 chloro­phen­yl) 6 methyl 3,4 di­hydro­pyrimidine 2(1H) thione

5 Acetyl 4 (4 chloro­phen­yl) 6 methyl 3,4 di­hydro­pyrimidine 2(1H) thione

... with the benzene ring. The thione, acetyl and methyl groups have equatorial orientations with respect to the attached heterocyclic ring. The chlorophenyl group has an axial orientation. Intermolecular N—H O, N—H S ... See full document

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(E) N′ (2 Chloro­benzyl­­idene) 1 methyl 4 nitro 1H pyrrole 2 carbohydrazide

(E) N′ (2 Chloro­benzyl­­idene) 1 methyl 4 nitro 1H pyrrole 2 carbohydrazide

... Cl1 0.1002 (9) 0.0517 (6) 0.1730 (14) 0.0028 (6) 0.0731 (9) −0.0179 (7) N1 0.0553 (16) 0.0427 (14) 0.0560 (18) −0.0065 (13) 0.0130 (13) 0.0045 (13) N2 0.057 (2) 0.102 (3) 0.057 (2) −0.019 (2) 0.0189 ... See full document

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tert Butyl 4 [2 (meth­oxy­carbonyl)­ethyl] 3,5 di­methyl 1H pyrrole 2 carboxyl­ate

tert Butyl 4 [2 (meth­oxy­carbonyl)­ethyl] 3,5 di­methyl 1H pyrrole 2 carboxyl­ate

... N 0.0523 (8) 0.0466 (7) 0.0401 (7) 0.0050 (6) −0.0003 (5) 0.0197 (6) O2 0.0556 (7) 0.0452 (6) 0.0624 (7) −0.0002 (5) −0.0110 (5) 0.0265 (5) C7 0.0480 (9) 0.0439 (8) 0.0605 (10) 0.0009 (7) 0.0014 (7) 0.0250 (8) C3 0.0497 ... See full document

8

Di­methyl 5 acetyl 1 hy­dr­oxy 4 methyl 1H pyrrole 2,3 di­carboxyl­ate, an oxidation resistant N hy­dr­oxy­pyrrole

Di­methyl 5 acetyl 1 hy­dr­oxy 4 methyl 1H pyrrole 2,3 di­carboxyl­ate, an oxidation resistant N hy­dr­oxy­pyrrole

... N1 0.0195 (3) 0.0176 (3) 0.0295 (4) −0.0019 (3) 0.0019 (3) −0.0014 (3) C1 0.0216 (4) 0.0181 (4) 0.0260 (4) 0.0008 (3) 0.0056 (3) 0.0002 (3) C2 0.0233 (4) 0.0185 (4) 0.0220 ... See full document

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4 Acetyl 2,3,4,5 tetra­hydro 1H 1,4 benzodiazepine

4 Acetyl 2,3,4,5 tetra­hydro 1H 1,4 benzodiazepine

... O1W 0.0770 (13) 0.0662 (11) 0.0596 (12) 0.0001 (9) −0.0051 (10) 0.0138 (10) C1 0.0511 (12) 0.0457 (12) 0.0412 (12) 0.0081 (10) 0.0042 (10) −0.0016 (10) C2 0.0669 (16) 0.0523 (13) 0.0547 (16) 0.0004 (12) 0.0037 (13) ... See full document

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1 Methyl N (2 {[(1 methyl 4 nitro 1H pyrrol 2 yl)carbonyl]amino}ethyl) 4 nitro 1H pyrrole 2 carboxamide di­methylformamide disolvate

1 Methyl N (2 {[(1 methyl 4 nitro 1H pyrrol 2 yl)carbonyl]amino}ethyl) 4 nitro 1H pyrrole 2 carboxamide di­methylformamide disolvate

... N1 0.0315 (17) 0.0252 (17) 0.0278 (17) −0.0125 (14) −0.0013 (13) 0.0009 (14) O3 0.054 (2) 0.0448 (18) 0.0339 (18) −0.0094 (15) −0.0017 (14) −0.0099 (14) C6 0.025 (2) 0.037 (2) 0.034 (2) ... See full document

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3 Methyl 1 tosyl 1H indole 2 carbaldehyde

3 Methyl 1 tosyl 1H indole 2 carbaldehyde

... O2B 0.0395 (12) 0.0464 (13) 0.0713 (14) −0.0175 (10) 0.0006 (10) 0.0051 (10) O3B 0.0653 (14) 0.0514 (14) 0.0607 (13) −0.0082 (11) −0.0325 (11) −0.0154 (10) S1B 0.0401 (4) 0.0355 (4) 0.0493 (4) ... See full document

12

3 Chloro 1 phenyl­sulfonyl 1H indole 2 carbaldehyde

3 Chloro 1 phenyl­sulfonyl 1H indole 2 carbaldehyde

... C7 0.099 (3) 0.054 (2) 0.168 (5) −0.005 (2) −0.063 (3) −0.034 (3) C8 0.115 (4) 0.051 (2) 0.219 (7) −0.034 (2) −0.071 (4) 0.005 (3) C9 0.082 (2) 0.085 (3) 0.129 (3) −0.043 ... See full document

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3 Phenyl­sulfanyl 1 phenyl­sulfonyl 1H indole 2 carbaldehyde

3 Phenyl­sulfanyl 1 phenyl­sulfonyl 1H indole 2 carbaldehyde

... S1 0.0747 (5) 0.0408 (4) 0.0640 (5) 0.0109 (3) 0.0088 (3) 0.0007 (3) S2 0.0481 (4) 0.0620 (4) 0.0724 (5) 0.0193 (3) −0.0109 (3) −0.0166 (4) N1 0.0521 (12) 0.0478 (11) 0.0482 (12) 0.0078 (10) ... See full document

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Ethyl 4 (2 chloro­quinolin 3 yl) 1 phenyl 1H pyrrole 3 carboxyl­ate

Ethyl 4 (2 chloro­quinolin 3 yl) 1 phenyl 1H pyrrole 3 carboxyl­ate

... C6 0.0617 (17) 0.078 (2) 0.117 (3) 0.0093 (17) 0.0390 (19) 0.025 (2) C8 0.083 (2) 0.094 (3) 0.078 (2) 0.0131 (19) 0.0467 (18) 0.0042 (18) C19 0.0695 (18) 0.125 (3) 0.0500 (16) 0.014 (2) ... See full document

9

1 (4 tert Butyl­benz­yl) 1H indole 3 carbaldehyde

1 (4 tert Butyl­benz­yl) 1H indole 3 carbaldehyde

... 1-Benzylindole-3-carbaldehyde readily undergoes base-catal- ysed condensation with azabicylo[2.2.2]octan-3-one (Sonar et al., 2003). However, 1-(4-tert-butylbenzyl)indole-3-carbalde- hyde failed to undergo ... See full document

7

Ethyl 4 (4 chloro­anilino) 1 (4 chloro­phen­yl) 2 methyl 5 oxo 2,5 di­hydro 1H pyrrole 2 carboxyl­ate

Ethyl 4 (4 chloro­anilino) 1 (4 chloro­phen­yl) 2 methyl 5 oxo 2,5 di­hydro 1H pyrrole 2 carboxyl­ate

... Lactam compounds or 2-pyrrolidinones are the aza analogues of lactones. Lactams have received relatively little attention in spite of the fact that they are potentially more effective in a pharmaceutical sense, ... See full document

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2 (N Phenyl­methane­sulfonamido)­ethyl 1H pyrrole 2 carboxyl­ate

2 (N Phenyl­methane­sulfonamido)­ethyl 1H pyrrole 2 carboxyl­ate

... The title compound was prepared by mixing 2-(phenylamino)ethyl-1H-pyrrole-2-carboxylate (1.0 g, 1.8 mmol), triethyl- amine (0.88 g, 8.8 mmol) and methanesulfonyl chloride (0.1 g, 8.8 mmol) in ... See full document

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