1-iodobutane

CCCCCCCCCCOc1cnc(-c2ccc(C=CC(OCCCC)C(F)(F)F)cc2)nc1
Reaction #1258
(-)-2-(4-(3-butoxy-4,4,4-trifluoro-1-butenyl)phenyl)-5-decyloxypyrimidine
Rendimiento 173.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCn1c(=O)c(-c2c(Cl)cccc2Cl)cc2cnc(N)nc21
Reaction #3273
2-amino-8-butyl-6-(2,6-dichlorophenyl)-8H-pyrido[2,3-d]pyrimidin-7-one
Rendimiento 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCn1ccc2cc(C(=O)OC)ccc21
Reaction #42435
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCn1ncc2ccc(C(=O)OC)cc21
Reaction #42442
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCn1ccc2c(N(C)S(C)(=O)=O)cc(C(=O)O)cc21
Reaction #42449
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCn1ccc2c(I)cc(C(=O)OC)cc21
Reaction #42455
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCn1ccc2ccc(C(=O)OC)cc21
Reaction #42499
methyl 1-butyl-1H-indole-6-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCOC(=O)c1ccc2ccn(CCCC)c2c1
Reaction #42503
butyl 1-butyl-1H-indole-6-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCC[C@@]1(C(=O)OC)CO[C@H](C(C)(C)C)N1C=O
Reaction #48542
title compound
Rendimiento 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCN1CCNCC1.Cl.Cl
Reaction #51230
N-butylpiperazine.dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCCCN(C(=O)C(C)C)c1ncc(C)o1
Reaction #54769
2-(N-butyl-isobutyramido)-5-methyloxazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CCCCC1(C(=O)O)CCC1
Reaction #55575
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CCCCC1(C(=O)O)CCC1
Reaction #57060
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCCCn1cc(SC2CCN(C)CC2)c2cc(Br)ccc21
Reaction #65175
5-bromo-1-butyl-3-[(1-methylpiperidin-4-yl)thio]1H-indole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCCCOc1ccc2c(C(=O)NCc3ccc(F)c(F)c3)c(C(C)C)n(Cc3ccccc3)c2c1
Reaction #68317
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCCCN(C(=O)OC(C)(C)C)C1CN(C(=O)OCc2ccccc2)C1
Reaction #72187
title compound
Rendimiento 48.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCCCn1c(=O)n(C2CCN(c3ncnc4cc(OC)c(OC)cc34)CC2)c(=O)c2cc([N+](=O)[O-])ccc21
Reaction #83286
Compound 4
Rendimiento 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCCCOc1cc(C(=O)OC)cc(C(=O)OC)c1
Reaction #87253
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCCCSc1ncccc1C(=O)O
Reaction #91127
title compound
Rendimiento 100.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCCCC(NC(=O)c1c(C)nc2c(OCc3c(F)cccc3F)cccn12)(C(=O)OCC)C(=O)OCC
Reaction #92770
diethyl butyl[({8-[(2,6-difluorobenzyl)oxy]-2-methylimidazo[1,2-a]pyridin-3-yl}carbonyl)amino]malonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
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