Busqueda de Subestructura

CN(N)c1nccs1

OCCCC1=NN(c2nc3ccccc3s2)C(O)(c2ccc(Cl)cc2)C1
Reaction #5109
title compound ( 1 )
DOI: 10.6084/m9.figshare.5104873.v1
CC1Cc2cc3c(cc2C(c2ccc([N+](=O)[O-])cc2)=NN1c1nccs1)OCO3
Reaction #53341
title compound
Rendimiento 80.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1csc(N2N=C(c3ccc([N+](=O)[O-])cc3)c3cc4c(cc3CC2C)OCO4)n1
Reaction #53342
title compound
Rendimiento 82.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cnc(N2N=C(c3ccc([N+](=O)[O-])cc3)c3cc4c(cc3CC2C)OCO4)s1
Reaction #53343
title compound
Rendimiento 66.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(N2N=C(c3ccc([N+](=O)[O-])cc3)c3cc4c(cc3CC2C)OCO4)sc1C
Reaction #53344
title compound
Rendimiento 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1csc(N2N=C(c3ccc([N+](=O)[O-])cc3)c3cc4c(cc3CC2C)OCO4)n1
Reaction #53345
title compound
Rendimiento 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1Cc2cc3c(cc2C(c2ccc([N+](=O)[O-])cc2)=NN1c1nc(C(=O)O)cs1)OCO3
Reaction #53359
title compound
Rendimiento 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCC(C(=O)N(c2cc(C#CC(C)(C)C)sc2C(=O)O)C2CCC(NN(C)c3nccs3)CC2)CC1
Reaction #67581
title compound
Rendimiento 14.7%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
CCN(CC)N(C(C)=O)c1nc2cc3nc(N)sc3cc2s1
Reaction #95383
2-(Diethylamino-acetylamino)-6-amino-benzo[1,2-d:5,4-d']bisthiazole
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)N(C(C)=O)c1nc2cc3nc(NC(=O)CCl)sc3cc2s1
Reaction #95384
2-(Diethylamino-acetylamino)-6-(chloroacetylamino)-benzo[1,2-d:5,4-d']bisthiazole
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 )
Rendimiento 47.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCc2nc(N3N=C(c4cc(F)ccc4F)SC3(CCO)c3ccccc3)sc2C1
Reaction #187248
DOI: 10.1039/C8SC04228D
NCCCC1(c2ccccc2)SC(c2cc(F)ccc2F)=NN1c1nc2c(s1)CNCC2
Reaction #291978
DOI: 10.1039/C8SC04228D
CN(NC(=O)c1ccccc1C(=O)O)c1nc(-c2ccccc2)cs1
Reaction #294004
DOI: 10.1039/C8SC04228D
CN1CCc2nc(N3N=C(c4cc(F)ccc4F)SC3(CCO[Si](c3ccccc3)(c3ccccc3)C(C)(C)C)c3ccccc3)sc2C1
Reaction #389612
DOI: 10.1039/C8SC04228D
CCN(CC)N(C(C)=O)c1nc2cc3nc(NC(=O)CCl)sc3cc2s1
Reaction #394068
DOI: 10.1039/C8SC04228D
CC1CCC(C(=O)N(c2cc(C#CC(C)(C)C)sc2C(=O)O)C2CCC(NN(C)c3nccs3)CC2)CC1
Reaction #423226
title compound
Rendimiento 14.7%DOI: 10.6084/m9.figshare.5104873.v1
CN(N=c1c2ccccc2[nH]c2cccc([N+](=O)[O-])c12)c1nccs1.Cl
Reaction #550869
1-nitro-9-acridanone methyl (2-thiazolyl)hydrazone hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Página 1Siguiente