部分構造検索

ClCCNCCc1ccccc1

COc1ccc(OC)c(C(=O)CNC(=O)CN=[N+]=[N-])c1
Reaction #11005
2-Azido-N-(β-oxo-2,5-dimethoxy phenehyl)acetamide
収率 91.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)CCl)[C@H](Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1ccccc1
Reaction #41320
2-Chloro-N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-phenyl-propan-2-yl]acetamide
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)C(Cl)Cl)[C@H](Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1ccccc1
Reaction #41321
2,2-Dichloro-N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-phenyl-propan-2-yl]acetamide
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)C(Cl)(Cl)Cl)[C@H](Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1ccccc1
Reaction #41322
2,2,2-Trichloro-N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-phenyl-propan-2-yl]acetamide
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)C(F)Cl)[C@H](Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1ccccc1
Reaction #41328
2-Chloro-2-fluoro-N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-phenyl-propan-2-yl]acetamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCl)NCCc1ccc2c(c1)OCO2
Reaction #51477
2-chloro-N-[2-(1,3-benzodioxol-5-yl)ethyl]acetamide
収率 74.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CNCCCO)NCCc1ccc2c(c1)OCO2
Reaction #51478
2-[(3-hydroxypropyl)amino]-N-[2-(1,3-benzodioxol-5-yl)ethyl]acetamide
収率 82.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(Cl)CNCCc1ccc(Cl)cc1.Cl
Reaction #158240
2-chloro-N-(4-chlorophenethyl)propan-1-amine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(Cl)CNCCc1ccc(Cl)cc1.Cl
Reaction #158241
2-chloro-N-(4-chlorophenethyl)propan-1-amine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Cc1ccccc1)NC(=O)CCl
Reaction #174400
DOI: 10.1039/C8SC04228D
CC(NC(=O)C(F)Cl)C(Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1ccccc1
Reaction #176073
DOI: 10.1039/C8SC04228D
CCN(CC)CCN1CCN(Cc2ccc(Cl)cc2)C(c2ccccc2)C1
Reaction #176163
DOI: 10.1039/C8SC04228D
CCCN1CC(c2cccc(OC)c2)OCC1=O
Reaction #181488
DOI: 10.1039/C8SC04228D
COC(=O)C(Cc1ccc(C)c(OC)c1)NC(=O)CNCc1ccccc1
Reaction #182743
DOI: 10.1039/C8SC04228D
CN1CCc2ccccc2CC1=O
Reaction #184320
DOI: 10.1039/C8SC04228D
O=C1C(Cl)=C(c2ccccc2)C(=O)N1Nc1ccccc1
Reaction #188249
DOI: 10.1039/C8SC04228D
CC(NC(=O)C(Cl)Cl)C(Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1ccccc1
Reaction #188793
DOI: 10.1039/C8SC04228D
Cc1ccc2c(-c3nnc(SCCN4CCc5cc6nc(C)oc6cc5CC4)n3C)cccc2n1
Reaction #201768
DOI: 10.1039/C8SC04228D
COc1ccc(CCN(C)CCOc2ccc([N+](=O)[O-])cc2N(C)C)cc1OC
Reaction #204165
DOI: 10.1039/C8SC04228D
c1ccc2c(c1)Cc1ccccc1N1CCN(CCN3CCNCC3)C[C@@H]21
Reaction #216929
title compound
収率 92.0%DOI: 10.6084/m9.figshare.5104873.v1
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