3-bromo-pentane

CC[CH](CC)[Sn]([CH3])([CH](CC)CC)[CH](CC)CC
Reaction #55937
yellow liquid
المردود 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CCOc1cc(I)cc(OC(CC)CC)c1Cl
Reaction #91042
2-Chloro-1-ethoxy-5-iodo-3-(pentan-3-yloxy)benzene
المردود 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCc1c2ccc(-c3ccnn3-c3ccc(S(C)(=O)=O)cc3)cc2nn1C(CC)CC
Reaction #184135
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC(CC)N1C(=O)CCC(c2cccc(Cl)c2)C1c1ccc(Cl)cn1
Reaction #208425
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CCC1(C)CC(c2cccc(Cl)c2)C(c2ccc(Cl)cc2)N(C(CSC(CC)CC)C2CC2)C1=O
Reaction #210478
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCc1cc(C#N)ccc1N=C1SCC2(CCCC2)N1C(CC)CC
Reaction #294132
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCC(CC)c1cc(C)nnc1NC(=O)C(C)(C)C
Reaction #313186
title compound
المردود 41454.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CCC(CC)c1cc(OC)nnc1NC(=O)C(C)(C)C
Reaction #313291
title compound
المردود 65.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CCc1cc(C#N)ccc1N=C1SCC2(CCCC2)N1C(CC)CC
Reaction #363771
2-(4-cyano-2-ethylphenylimino)-1-(3-pentyl)-3-thia-1-azaspiro[4.4]nonane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CCC(CC)C(O)c1c(O)cc(C(C)C)c(OC(C)=O)c1C(C)C
Reaction #399590
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCC(CC)Oc1ccc(C(=O)OC)c(O)c1
Reaction #408056
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCC(CC)n1ncc(-c2ccc(OC)c(OC3CCCC3)c2)cc1=O
Reaction #511792
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
CCC(CC)Oc1cc(-c2nc(CCC(=O)c3ncccc3C)co2)ccc1OC
Reaction #562794
3-{2-[3-(1-ethylpropoxy)-4-methoxy phenyl]oxazol-4-yl}-1-(3-methylpyridin-2-yl)propan-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
CCC(CC)Oc1cc(-c2nc(CNC(=O)c3ncccc3C)co2)ccc1OC
Reaction #562799
N-{2-[3-(1-ethylpropoxy)-4-methoxy phenyl]oxazol-4-ylmethyl}-3-methylpicolinamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
CCOc1ccccc1C(=O)NCc1coc(-c2ccc(OC)c(OC(CC)CC)c2)n1
Reaction #562800
2-ethoxy-N-{2-[3-(1-ethylpropoxy)-4-methoxyphenyl]oxazol-4-ylmethyl}benzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
CCC(CC)Oc1cc(-c2nc(CNC(=O)c3ncccc3C)co2)ccc1OC(F)F
Reaction #562815
N-{2-[4-difluoromethoxy-3-(1-ethylpropoxy)phenyl]oxazol-4-ylmethyl}-3-methylpicolinamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
CCOc1ccccc1C(=O)NCc1coc(-c2ccc(OC(F)F)c(OC(CC)CC)c2)n1
Reaction #562824
N-{2-[4-difluoromethoxy-3-(1-ethylpropoxy)phenyl]oxazol-4-ylmethyl}-2-ethoxybenzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
CCOc1cc(C=O)ccc1OC(CC)CC
Reaction #635105
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
CCC(CC)n1cnc([N+](=O)[O-])c1
Reaction #640267
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
—
Reaction #668564
liquid
المردود 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_07
الصفحة 1التالي