子结构搜索

CCSCCCl

CC(C)NCCS(=O)(=O)Cc1ccccc1.Cl
Reaction #4303
white crystalline solid
收率 65.8%DOI: 10.6084/m9.figshare.5104873.v1
FC(Sc1ccccc1Cl)C(F)(F)F
Reaction #4837
1-chloro-1,2,2,2-tetrafluoroethylthiobenzene
DOI: 10.6084/m9.figshare.5104873.v1
CCSCCOc1cc(C)c(-c2cccc(CO)c2)c(C)c1
Reaction #43917
title compound
收率 47.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)Oc1ccc(Cl)cc1)[C@H]1CC[C@H](CSCCCl)CC1
Reaction #53851
trans-[4-(2-Chloro-ethylsulfanylmethyl)-cyclohexyl]-methyl-carbamic acid 4-chloro-phenyl ester
收率 104.7%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CCO)CCSC[C@H]1CC[C@H](N(C)C(=O)Oc2ccc(Cl)cc2)CC1
Reaction #53852
trans-(4-{2-[Ethyl-(2-hydroxy-ethyl)-amino]-ethylsulfanylmethyl}-cyclohexyl)-methyl-carbamic acid 4-chloro-phenyl ester
DOI: 10.6084/m9.figshare.5104873.v1
NC(C(=O)N[C@@H]1C(=O)N2C(C(=O)O)=C(Cl)CS[C@H]12)c1ccccc1
Reaction #56083
7β-(α-phenyl-glycinamido)-3-chloro-3-cephem-4-carboxylic acid
收率 91.4%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)C(SCCCl)SCCCl
Reaction #64074
4c
收率 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)N[C@H]1CC[C@H](O[N+](=O)[O-])CC1
Reaction #64248
trans-N-propionyl-4-nitroxycyclohexylamine
收率 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cccc(C(C)C)c1NC(=O)CS(=O)(=O)CCN1CCN(c2ccccc2)CC1
Reaction #65043
title compound
收率 70.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1csc(-c2ncccc2O)n1)NC1C(=O)N2C(C(=O)O)=C(Cl)CSC12
Reaction #81862
9j
收率 90.2%DOI: 10.6084/m9.figshare.5104873.v1
C=CS(=O)(=O)C(CCCCCCC(=O)O)CCCC(O)CCCCC
Reaction #93918
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CS(=O)(=O)C(CCCCCCC(=O)O)CCCC(O)CCCCC
Reaction #93919
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(Cl)CS[C@@H]2C(NC(=O)COc3ccccc3)C(=O)N2C1C(=O)O
Reaction #94054
7-phenoxyacetoamido-3-chloro-3-methyl-cepham-4-carboxylic acid
收率 51.5%DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)CSCC(=O)OC
Reaction #94358
methyl 2-(3-methylacetonylmercapto)acetate
收率 60.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(N)c(Cl)cc1C(=O)NCC1CCN(CCS(=O)(=O)Cc2ccccc2)CC1
Reaction #180780
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)C1CCC(CC#N)S1
Reaction #192334
DOI: 10.1039/C8SC04228D
COC(=O)C(NC(=O)C1CCCS1)C(C)C
Reaction #201681
DOI: 10.1039/C8SC04228D
O=C(Cl)C1SCCN1S(=O)(=O)c1ccc(-c2ccccc2)cc1
Reaction #202643
DOI: 10.1039/C8SC04228D
O=C(Cl)CSCCOc1ccccc1
Reaction #204007
DOI: 10.1039/C8SC04228D
CON=C(C(=O)N[C@@H]1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=CCS[C@H]12)c1nc(N)sc1Cl
Reaction #214083
7β-[2-(2-amino-5-chloro-4-thiazolyl)-2-methoxyiminoacetamido]-3-cephem-4-carboxylic acid diphenylmethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
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