部分構造検索

C(CCl)N.Cl

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
CN1CCN(CCCl)CC1.Cl
Reaction #45263
1-(2-chloroethyl)-4-methylpiperazine hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
C=CC(N)(CCC(=O)O)C(=O)NC1C(=O)N2C(C(=O)O)=C(COC(C)=O)CSC12
Reaction #54311
7-[[2-amino-4-carboxy-2-vinylbutyryl]amino]-3-acetyloxymethyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccsc1NC(=O)NC(=O)C(Cl)(Cl)Cl
Reaction #58622
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Br)sc1NC(=O)NC(=O)C(Cl)(Cl)Cl
Reaction #58623
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC[C@H]1O[C@@H](O[C@@H]2[C@H](OCc3ccccc3)[C@@H](OCc3ccccc3)[C@H](C)O[C@H]2O)[C@H](NC(=O)C(Cl)(Cl)Cl)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #90567
318
収率 83.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC[C@H]1O[C@@H](O[C@H]2[C@H](OC(=N)C(Cl)(Cl)Cl)O[C@@H](C)[C@H](OCc3ccccc3)[C@H]2OCc2ccccc2)[C@H](NC(=O)C(Cl)(Cl)Cl)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #90568
306
収率 79.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1c2nc(C(=O)OC)cc(NC(=O)C(Cl)(Cl)Cl)c2cc2c(=O)cc(C(=O)OCC)oc12
Reaction #93769
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1c2nc(C(=O)OC)cc(N)c2cc2c(=O)cc(C(=O)OCC)oc12
Reaction #93770
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(Cl)=C(Cl)C(=O)N1c1ccc(Oc2ccccc2)cc1
Reaction #93841
N-(p-phenoxyphenyl)-2,3-dichloromaleimide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCl)Nc1nc2cc3nc(NC(=O)CCl)sc3cc2s1
Reaction #95379
2,6-bis-(chloroacetyl-amino)-benzo[1,2-d:5,4-d']bisthiazole
収率 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)N(C(C)=O)c1nc2c(C)c3nc(N(C(C)=O)N(CC)CC)sc3cc2s1
Reaction #95381
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)N(C(C)=O)c1nc2cc3nc(N(C(C)=O)N(CCC)CCC)sc3cc2s1.Cl.Cl
Reaction #95385
2,6-Bis-(di-n-propylamino-acetylamino)-benzo[1,2-d:5,4-d']bisthiazole dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCC1CCCCN1N(C(C)=O)c1nc2cc3nc(N(C(C)=O)N4CCCCC4CC)sc3cc2s1
Reaction #95386
compounds ( a )
収率 47.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #172842
solid
収率 83.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccccc1CCN1CCN(CCCc2ccccc2)CC1
Reaction #179248
DOI: 10.1039/C8SC04228D
CCSC(NC(=O)c1ccccc1OC(C)=O)C(Cl)(Cl)Cl
Reaction #185236
DOI: 10.1039/C8SC04228D
O=C(C(Cl)Cl)N1CCN(c2ccc([N+](=O)[O-])cc2)CC1
Reaction #190050
DOI: 10.1039/C8SC04228D
CCOP(=O)(OCC)C(CCCNC(=O)CCCc1ccccc1N(CCCl)CCCl)P(=O)(OCC)OCC
Reaction #194242
DOI: 10.1039/C8SC04228D
COc1cc(N2CCN(C(=O)Cn3nc(-c4ccccn4)c(Cl)c3C)C(C)C2)c(F)cc1Cl
Reaction #196339
DOI: 10.1039/C8SC04228D
1 ページ次のページ