α-methyl cinnamic acid

CC(Cc1ccccc1)C(=O)O
Reaction #1292
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(Cc1ccccc1)C(=O)O
Reaction #1428
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=Cc1ccccc1)C(=O)Nc1ccc2nc(N3CCC(N(C)C)C3)sc2c1
Reaction #198515
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=Cc1ccccc1)C(=O)Nc1cccc(Cl)c1
Reaction #210900
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(Cc1ccccc1)C(=O)O
Reaction #352161
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
CC(=Cc1ccccc1)C(=O)NCCN=[N+]=[N-]
Reaction #379826
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(Cc1ccccc1)C(=O)O
Reaction #429440
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
CC(Cc1ccccc1)C(=O)O
Reaction #429456
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
CC(Cc1ccccc1)C(=O)O
Reaction #430230
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
CCn1c(=O)c2[nH]c(/C(C)=C/c3ccccc3)nc2n(CC)c1=O
Reaction #462531
Compound 134
المردود 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_01
CC(=Cc1ccccc1)C(N)=O
Reaction #759562
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CC(Cc1ccccc1)C(=O)O
Reaction #829040
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_09
CC(C(=O)O)[CH](c1ccccc1)[Ge]([Cl])([Cl])[Cl]
Reaction #924633
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
O=C(O)c1ccccc1
Reaction #1093489
Benzoic acid
المردود 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_09
C/C(=C\c1ccccc1)C(N)=O
Reaction #1131941
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
CCn1c(=O)c2[nH]c(/C(C)=C/c3ccccc3)nc2n(CC)c1=O
Reaction #1164689
Compound 133
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_08
CCn1c(=O)c2[nH]c(/C(C)=C/c3ccccc3)nc2n(CC)c1=O
Reaction #1169006
Compound 134
المردود 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_12
O=C(O)c1ccccc1
Reaction #1202863
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
CC(Cc1ccccc1)C(=O)O
Reaction #1208631
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
CC(=Cc1ccccc1)C(=O)Cl
Reaction #1227827
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
الصفحة 1التالي