1-hexyne

CCCCC#Cc1ccc(OC)cc1CCN(C)C.Cl
Reaction #4382
2-(1-hexynyl)-5-methoxy-N,N-dimethylbenzeneethanamine hydrochloride
Ausbeute 27.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCCCC#CC(C)(O)c1ccc(-c2ccc(F)cc2)cc1
Reaction #54993
2-(4'-fluoro-4-biphenylyl)-3-octyn-2-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CCCCC#CC(C)(O)c1ccc(-c2ccc(F)cc2)cc1
Reaction #54994
2-(4'-fluoro-4-biphenylyl)-3-octyn-2-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CCCCC#CC(=O)c1ccc(Br)cc1
Reaction #65481
1-(4-bromophenyl) 2-heptyn-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCCCC=CSC=CCCCC
Reaction #94491
(1-hexenyl) sulfide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
CCCCC=CC(O)C(C)C
Reaction #212446
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCC#CC(CC(C)C)N(Cc1ccccc1)Cc1ccccc1
Reaction #237893
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCC#Cc1cccc(-n2nc(CC)c(C(=O)OC)c2CC)c1
Reaction #245694
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCC=CC(O)CC
Reaction #254126
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCC#CC(=O)c1ccc(Br)cc1
Reaction #353232
1-(4-bromophenyl) 2-heptyn-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
CCCCc1cc(C(F)(F)F)n[nH]1
Reaction #357961
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
CCCCC#Cc1cc2c(cc1Br)C(C)(C)CCC2(C)C
Reaction #382869
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCCC#Cc1cn(S(=O)(=O)c2ccccc2)nc1-c1cccnc1
Reaction #388905
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCCC=CC(O)c1ccc(C(F)(F)F)cc1
Reaction #394333
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCCC#Cc1cccc(C=O)c1
Reaction #396722
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCCC#Cc1cncc(OC[C@@H]2CCCN2C)c1
Reaction #452988
oil
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
CCCCC#Cc1cncc(OC[C@@H]2CCN2)c1.Cl.Cl
Reaction #453015
title compound
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
CCCCC#C[Si](CCl)(c1ccc(F)cc1)c1ccc(F)cc1
Reaction #458491
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_07
CCCCC#CC(=O)C(C)O
Reaction #460643
2-hydroxy-4-nonyn-3-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_11
CCCC/C(C)=C/CO
Reaction #464247
alcohol
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
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