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Cc1cccc(-c2ccccc2N)c1

N#CC(=NNc1ccccc1-c1ccccc1)C(=O)NCC1CC1
Reaction #59369
title compound
المردود 36.1%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(-c2ccccc2-c2cccs2)cc1
Reaction #74920
2-(o-biphenylyl)thiophene
المردود 34.8%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #90324
solid
المردود 87.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1ccc(-c2ncn(-c3ccc(OC(F)(F)F)cc3)n2)cc1)Nc1ccccc1-c1ccccc1
Reaction #90332
title compound
المردود 28.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cnc(Nc2ccccc2-c2ccccc2)nc1Nc1ccccc1-c1ccccc1
Reaction #158554
N2,N4-bis(2-phenylphenyl)-5-methyl-2,4-pyrimidinediamine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cnc(Nc2ccccc2-c2ccccc2)nc1Nc1ccccc1-c1ccccc1
Reaction #163663
N2,N4-bis(2-phenylphenyl)-5-methyl-2,4-pyrimidinediamine
DOI: 10.6084/m9.figshare.5104873.v1
O=c1c(Nc2ccccc2O)c(Nc2ccccc2-c2ccccc2)c1=O
Reaction #186854
DOI: 10.1039/C8SC04228D
Cc1cccc(-c2ccccc2NC(=N)N2CCCCC2)c1
Reaction #188167
DOI: 10.1039/C8SC04228D
Cc1ccc(-c2ccccc2NC(=N)N(C)C)cc1
Reaction #201273
DOI: 10.1039/C8SC04228D
CSc1cccc(-c2ccccc2N)c1
Reaction #207404
DOI: 10.1039/C8SC04228D
O=[N+]([O-])N=C1NCCN1C=Nc1ccccc1-c1ccccc1
Reaction #265285
DOI: 10.1039/C8SC04228D
CNC(=S)Nc1ccccc1-c1ccccc1
Reaction #265513
DOI: 10.1039/C8SC04228D
S=C=Nc1ccccc1-c1ccccc1
Reaction #266028
DOI: 10.1039/C8SC04228D
Nc1ccccc1-c1ccccc1
Reaction #266905
DOI: 10.1039/C8SC04228D
N=C(Nc1ccccc1-c1ccccc1)N1CCOCC1
Reaction #292231
DOI: 10.1039/C8SC04228D
Cc1cnc(Nc2ccccc2-c2ccccc2)nc1Nc1ccccc1-c1ccccc1
Reaction #313823
N2,N4-bis(2-phenylphenyl)-5-methyl-2,4-pyrimidinediamine
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #342136
compound
المردود 61.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccccc1-c1ccccc1
Reaction #372407
DOI: 10.1039/C8SC04228D
CCOC(=O)CCCCCNc1ccccc1-c1ccccc1
Reaction #382667
DOI: 10.1039/C8SC04228D
Ic1ccccc1-c1ccccc1
Reaction #384735
DOI: 10.1039/C8SC04228D
الصفحة 1التالي