1-iodoheptane

CCCCCCCSC1=Nc2ccc(C#Cc3ccc(C(=O)OCC)cc3)cc2C(C)(C)C1
Reaction #80718
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCCCCCCN1C(=O)CC(C)(C)c2cc(C#Cc3ccc(C(=O)OCC)cc3)ccc21
Reaction #80733
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCCCCCCOc1ccc2c(c1)Nc1cccc(S(=O)(=O)N(C)C)c1S2
Reaction #225092
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCCN(CCc1csc(SC(C)(C)C(=O)OC(C)(C)C)n1)c1ncc(Br)cn1
Reaction #232853
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCCSc1nnc(N)s1
Reaction #251622
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCCN(CCc1csc(SC(C)(C)C(=O)OC(C)(C)C)n1)c1ncc(CC)cn1
Reaction #260429
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCCOc1cc(I)ccc1C(=O)OC
Reaction #282613
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cl
Reaction #301393
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCCCCOc1ccc(C(=O)OC)cc1OCCCCCCC
Reaction #335194
desired product
المردود 198.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
CCCCCCCN(CCc1csc(SC(C)(C)C(=O)OC(C)(C)C)n1)c1ncc(C(=O)OC)cc1Cl
Reaction #370825
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCCCCCNCc1ccc(CNC(=O)NC(C)(C)C)cc1
Reaction #394034
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCCCCCN1C(=O)C2CC2C1=O
Reaction #453716
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
CCCCCCCN1CCC(O)CC1
Reaction #481681
1-Heptyl-4-hydroxypiperidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
CCCCCCCOc1ccc(-c2ccc(C(=O)OC3CCC(C#N)(CCCCCCC)CC3)cc2)cc1
Reaction #564478
4-cyano-4-heptylcyclohexyl 4-heptyloxy-4'-biphenylcarboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_12
CCCCCCC[n+]1c2ccccc2n2c(C)csc21.[I-]
Reaction #689752
9-heptyl-3-methyl[1,3]thiazolo[3,2-a]benzimidazol-9-ium iodide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
CCCCCCC[n+]1c(C)sc2ccccc21.[I-]
Reaction #698626
3-heptyl-2-methylbenzothiazolium iodide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_12
CCCCCCCOc1ccc2cc(Br)ccc2n1
Reaction #797090
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
CCCCCCCOc1nsc(NC(=O)N(C)C)c1C(N)=O
Reaction #837741
5-(3,3-Dimethyl-ureido)-3-heptyloxy-isothiazole-4-carboxylic Acid Amide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_07
CCCCCCCN(CCc1csc(SC(C)(C)C(=O)OC(C)(C)C)n1)c1ccc(Br)cn1
Reaction #892348
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCCCCCCNc1c(F)c(C)c(F)c2oc(-c3ccc(NC(=O)C(C)(C)C)c(F)c3)cc(=O)c12
Reaction #919400
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
الصفحة 1التالي