Recherche de Sous-structure

2248

Cc1ccccc1CNC1CN(C)C(=O)c2cc(Cl)cnc2O1.O=C(O)C(=O)O
Reaction #4960
white crystals
Rendement 47.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(O)(CC(=O)c1ccc(C)c(F)c1)C(=O)OCC
Reaction #8005
title compound
Rendement 79.3%DOI: 10.6084/m9.figshare.5104873.v1
CCNc1nccc(C(=O)CC(O)(C(=O)OCC)C(=O)OCC)n1
Reaction #40546
Diethyl 2-[2-(2-ethylaminopyrimidin-4-yl)-2-oxo-ethyl]-2-hydroxy-malonate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1[nH]c(-c2cccc3ccccc23)nc1C
Reaction #40746
5-methyl-2-naphthalen-1-yl-3H-imidazole-4-carboxylic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=NN(C)C(=O)CC)C(=O)OCC
Reaction #44242
desired product
Rendement 49.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)Nc1nc2ccccc2s1
Reaction #54746
desired product
Rendement 44.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(=O)c1ccc(C2CCCCC2)c(S)c1
Reaction #54833
3-mercapto-4-cyclohexylphenylglyoxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)c1ccc(C2CCCCC2)c(SC)c1
Reaction #54834
ethyl 3-methylthio-4-cyclohexylphenylglyoxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC2=C(CSc3ccccc32)C1=O
Reaction #62612
brown crystalline solid
Rendement 82.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CC(=O)O)C(=O)OCC
Reaction #64699
aimed product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)N1CCc2ccccc21
Reaction #80737
N-ethoxalylindoline
Rendement 108.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)N1CCc2cc(Br)ccc21
Reaction #80738
5-bromo-N-ethoxalylindoline
Rendement 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(O)(C(=O)OCC)c1cc(C)ccc1C
Reaction #83842
diethyl (2,5-dimethylphenyl)-hydroxymalonate
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc2c(CCCN3CCN(c4ccccc4)CC3)noc2c1.O=C(O)C(=O)O
Reaction #92891
1-[3-(6-Fluoro-1,2-benzisoxazol-3-yl)propyl]-4-phenylpiperazine oxalate
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc2c(CCCN3CCN(c4ccccc4)CC3)noc2c1.O=C(O)C(=O)O
Reaction #93150
1-[3-(6-Fluoro-1,2-benzisoxazol-3-yl)propyl]-4-phenylpiperazine oxalate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CCC2(CCN(C(=O)N(C)C(C)c3cc(C(F)(F)F)cc(C(F)(F)F)c3)C(c3ccc(F)cc3C)C2)N1
Reaction #174113
DOI: 10.1039/C8SC04228D
CC(C)CC(NC(=O)C(Cc1c[nH]cn1)NC(CCc1ccccc1)C(=O)O)C(=O)O
Reaction #175608
DOI: 10.1039/C8SC04228D
O=C(O)C(=O)c1sccc1Nc1c(Cl)cccc1Cl
Reaction #194206
DOI: 10.1039/C8SC04228D
CCCCOC(=O)C(=O)OCCCC
Reaction #200424
DOI: 10.1039/C8SC04228D
NS(=O)(=O)c1ccc(OCCOc2ccc(C(=O)C(=O)O)cc2)cc1
Reaction #203263
DOI: 10.1039/C8SC04228D
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