hexane ethyl acetate

COc1ccc(C(O)Cc2ccncc2)cc1OC1CCCC1
Reaction #1017
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1cc(-c2ccc(Cl)cc2)ccc1=O
Reaction #1603
5-(4-chlorophenyl)-1-(2-pentyn-1-yl)-2-pyridinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1cc(-c2ccc(Cl)cc2)ccc1=O
Reaction #1670
5-(4-chlorophenyl)-1-(2-pentyn-1-yl)-2-pyridinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1cc(-c2ccc(Cl)cc2)ccc1=O
Reaction #2175
5-(4-chlorophenyl)-1-(2-pentyn-1-yl)-2-pyridinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1cc(-c2ccc(Cl)cc2)ccc1=O
Reaction #2216
5-(4-chlorophenyl)-1-(2-pentyn-1-yl)-2-pyridinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC#CCn1cc(-c2ccc(Cl)cc2)ccc1=O
Reaction #2274
5-(4-chlorophenyl)-1-(2-pentyn-1-yl)-2-pyridinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)O[C@@H]1C=C[C@H](O[Si](C)(C)C(C)(C)C)C1
Reaction #2653
title compound
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCC#CC#CCOc1ccc(C(=O)OCC)cc1
Reaction #2735
ethyl 4-(2,4-nonadiynyloxy)-benzoate
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC=CCCC(=O)C(C(=O)OC)C(C[N+](=O)[O-])c1ccc2c(c1)OCO2
Reaction #3099
title compound
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc2c(O)cccc2n1Cc1cccc2ccccc12
Reaction #3455
4-hydroxy-2-methyl-1-[(1-naphthalenyl)methyl]-1H-indole
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)C(C(=O)Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)cc1)c1ccccc1
Reaction #3689
beige solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1[C@@H](N2C(=O)c3ccccc3C2=O)Cc2ccccc2C2CCC=CN12
Reaction #3771
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1[C@@H](N2C(=O)c3ccccc3C2=O)Cc2ccccc2C2CCC=CN12
Reaction #3772
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)[C@@H]1CCCC2c3ccccc3CC(N3C(=O)c4ccccc4C3=O)C(=O)N21
Reaction #3773
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCC/C=C\CCCCCCCCNC(=O)OC(CCCO)COC/C=C(\C)CCC=C(C)C
Reaction #5350
(Z)-9-octadecenylcarbamic acid (E)-1-[[(3,7-dimethyl-2,6-octadienyl)oxy]methyl]-4-hydroxybutyl ester
Ausbeute 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCCCCCCC/C=C\CCCCCCCCNC(=O)OC(CCC(=O)O)COC/C=C(\C)CCC=C(C)C
Reaction #5351
5-[((E)-3,7-dimethyl-2,6-octadienyl)oxy]-4-[[((Z)-9-octadecenylamino) carbonyl]oxy]pentanoic acid
Ausbeute 30.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
N#Cc1c(N)oc2c1c(Cc1ccccc1)c(O)c1ccccc12
Reaction #5583
product
Ausbeute 38.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCC(C)(CN=[N+]=[N-])NC(=O)OCc1ccccc1
Reaction #5652
1-Azido-2-(benyloxycarbonylamino)-2-methylbutane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COC(=O)C(c1cn(Cc2ccc(Cl)cc2)c2ccccc12)N(C)Cc1cccc(C(F)(F)F)c1
Reaction #5707
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(C)=CCCC(C)=CC=C(C#N)C(C)C
Reaction #5759
2-(1-methylethyl)-5,9-dimethyl-2,4,8-decatrienenitrile
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
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