1-iodohexane

CCCCCCOc1cc2ccc(-c3ccc(C(=O)OC)c(O)c3)cc2cc1C12CC3CC(CC(C3)C1)C2
Reaction #1230
methyl 2-hydroxy-4-[7-(1-adamantyl)-6-hexyloxy-2-naphthyl]benzoate
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCN(C(=O)C(C)C)c1sc(CC)cc1C(=O)OCC
Reaction #55940
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CCCCCCOc1ccc2[nH]c(C)c(CC(=O)O)c2c1
Reaction #65985
white crystals
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCCCCCOc1ccc2c(C(=O)NCc3ccc(F)c(F)c3)c(C(C)C)n(Cc3ccccc3)c2c1
Reaction #68319
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCCCCCOc1ccc(S(=O)(=O)N(CC(=O)OCC)CC(C)C)cc1
Reaction #177261
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCNc1c(F)cc(F)c2oc(-c3ccc(N(CCCN4C(=O)c5ccccc5C4=O)C(C)=O)c(F)c3)cc(=O)c12
Reaction #187223
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCN1C(=O)N=C(P(=O)(OCC)OCC)C1=O
Reaction #195708
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCC(C(=O)OC)(C(=O)OC)c1ccc(Oc2ccccc2)cc1
Reaction #203935
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCN1CCC(NC(=O)C2c3ccccc3Oc3ccccc32)CC1
Reaction #204852
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCOc1ccc2cc(-c3nnc(CCCCCC)s3)ccc2c1
Reaction #211243
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCOc1ccc(-c2cnc(-c3ccc(CCCCCC)cc3)s2)cc1F
Reaction #232733
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCOCCOc1ccc(Br)cc1
Reaction #235094
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCNc1c(F)cc(F)c2oc(-c3ccc(NC(=O)C(C)(C)C)c(F)c3)cc(=O)c12
Reaction #253788
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCN1C(=O)c2cscc2Nc2ccccc21
Reaction #259533
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCOC(=O)c1ccc(OCCCCCCc2cccc(O)c2O)c(CCC)c1O
Reaction #260553
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCOc1ccc(-c2nnc(-c3ccc(CCCCCC)cc3)s2)cc1F
Reaction #269467
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCCCOC(=O)C1=COC(OC(=O)NC)C2C1CC1OC12C
Reaction #281597
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCCCOc1ccc(C2CCC(CCCCC)CO2)cc1
Reaction #292625
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCCCCC(=O)CC(=O)c1ccccc1
Reaction #295641
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCCCN(C(=O)OC(C)(C)C)n1cccc1
Reaction #298461
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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