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CCCCN(CCCC)CCCC

CCOC(=O)CC(=O)COCC1OC(C)(C)OC1COCC(=O)CC(=O)OCC
Reaction #1344
title compound
Ausbeute 43.7%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)(C)c1ccc(S(=O)(=O)Nc2ncnc(OCCOc3ccc(Br)cn3)c2-c2ccc(C)cc2)cc1
Reaction #2367
4-tert-amyl-N-{6-[2-(5-bromopyridin-2-yloxy)ethoxy]-5-(4-methylphenyl)pyrimidin-4-yl}benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
BrCCCCCCOCCc1ccccc1
Reaction #5304
title compound
Ausbeute 55.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CCOCCCCCCBr)cc1
Reaction #5313
oil
Ausbeute 237.5%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(CCOCCCCCBr)cc1
Reaction #5314
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CCCOCCCCCBr)cc1
Reaction #5315
oil
Ausbeute 244.6%DOI: 10.6084/m9.figshare.5104873.v1
Clc1cccc(Cl)c1CSCc1c(Cl)cccc1Cl
Reaction #6382
bis(2,6-dichlorobenzyl) sulfide
Ausbeute 80.4%DOI: 10.6084/m9.figshare.5104873.v1
CCN1c2ccccc2Sc2ccccc21
Reaction #6673
10-Ethylphenothiazine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=CN(c1ccc(F)c(F)c1F)[C@@H](C)CO)C(=O)OCC
Reaction #8569
title compound
Ausbeute 92.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=CN(c1ccc(F)c(F)c1F)[C@@H](C)CO)C(=O)OCC
Reaction #8570
title compound
Ausbeute 90.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=CN1c2ccc(F)c(F)c2OC[C@@H]1C)C(=O)OCC
Reaction #8572
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=CN1c2ccc(F)c(F)c2OC[C@@H]1C)C(=O)OCC
Reaction #8576
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CN1C(=O)C2=C(CCCC2)C1=O)C(C)=O
Reaction #10980
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COCCCN(N=C(C)C)C(=O)OC(C)(C)C
Reaction #41184
N′-isopropylidene-N-(3-methoxypropyl)-hydrazinecarboxylic acid tert-butyl ester
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC[N+](CCCC)(CCCC)CCCC.O=S([O-])c1cccc2ccccc12
Reaction #43891
Tetrabutylammonium 1-Naphthalene Sulfinate
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](OCc1ccccc1)[C@H]1COCC(=O)N1
Reaction #44648
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(I)cc1
Reaction #46962
title compound
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(C(F)(F)F)cc(Cl)n1
Reaction #48083
gray liquid
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OP(=O)(OCCl)OC(C)(C)C
Reaction #48490
di-tert-butyl chloromethyl phosphate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCN(CCCCCCCCCCCCCCCCCC)C(=O)CCC(C)C1CCC2C3CCC4CC(OC(=O)ON5C(=O)CCC5=O)CCC4(C)C3CCC12C
Reaction #49205
Compound 83
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1
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