#4524230

NCCC1CN(C(c2ccccc2)c2ccccc2)C1
Reaction #968
title compound
收率 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOP(=O)(OCC)C(CC(=O)CC)P(=O)(OCC)OCC
Reaction #2066
title compound
收率 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCNC(=O)CC(P(=O)(OCC)OCC)P(=O)(OCC)OCC
Reaction #2068
title compound
收率 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccc2cccc(CCO)c2c1
Reaction #2980
2-(7-METHOXY-1-NAPHTHYL)ETHANOL
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(C)CCC(C)(C)c2cc(C#Cc3ccc(CO)cn3)ccc21
Reaction #6084
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
N#Cc1ccc(N(Cc2ccc(F)c(OC(=O)c3ccccc3)c2)n2cnnc2)cc1
Reaction #48215
Benzoic Acid 5-{[(4-cyano-phenyl)-[1,2,4]triazol-4-yl-amino]methyl}-2-fluoro-phenyl Ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)[C@H]1C[C@@H](O)C1
Reaction #48668
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1cnc(CN2CCNC2=C[N+](=O)[O-])cn1
Reaction #50492
1-(2-methyl-5-pyrazinylmethyl)-2-(nitromethylene)imidazolidine
收率 23.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CCN(C)C(=O)C1=CC(C)(C)Oc2ccc([N+](=O)[O-])cc21
Reaction #64356
N-ethyl-N-methyl-6-nitro-2,2-dimethyl-2H-1-benzopyran-4-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
c1ccc(COC2CCCCCCCCCCC2)cc1
Reaction #64745
Phenylmethoxycyclododecane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCCSc1ncc(CO)n1Cc1ccccc1Cl
Reaction #65271
1-(2-chlorophenyl)methyl-5-hydroxymethyl-2-propylthio-1H-imidazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
O=Cc1ccc([N+](=O)[O-])cn1
Reaction #71352
title compound
收率 49.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC1=C(C)C(=O)C(C)CC1
Reaction #94087
2,3,6-trimethyl-2-cyclohexen-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
Cl.FC(F)(F)c1ccc(Cl)c(C23CNCC2C3)c1
Reaction #94565
1-(4-chloro-α,α,α-trifluoro-m-tolyl)-3-azabicyclo[3.1.0]hexane hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
O=CCCCCCCBr
Reaction #95933
title compound
收率 85.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CCc1c(OC)nc(OC)nc1C(=O)c1cc(Cl)cc(Cl)c1
Reaction #173117
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(COc1ccc(C(N)=O)cn1)NCc1ccccc1
Reaction #173125
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(C2(O)CCC3CN(Cc4ccccc4)CCC3C2)cc1
Reaction #173130
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1(C)Cc2cc(C(=O)NS(C)(=O)=O)ccc2NC1c1cccc(N2CCNCC2)c1
Reaction #173149
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CNc1cc(C)ccc1O
Reaction #173180
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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