N-methylformanilide

CC(C)(C)c1cc(C=O)ccc1O
Reaction #3047
desired subtitled intermediate
Yield 22.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)c1cc(C=O)ccc1O
Reaction #3050
3-(1,1-dimethylethyl)-4-hydroxybenzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=Cc1cc(F)ccc1F
Reaction #4064
product
Yield 77.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
Cc1c(O)ccc(C=O)c1O
Reaction #4980
product
Yield 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CN(C=Nc1nccs1)c1ccccc1
Reaction #5245
crude product
Yield 94.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CN(C=Nc1ccccn1)c1ccccc1
Reaction #5246
3
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=CC(=O)N(C)c1ccccc1
Reaction #10029
pure compound
Yield 70.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=CC(=O)N(C)c1ccccc1
Reaction #10030
pure compound
Yield 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=CC(=O)N(C)c1ccccc1
Reaction #10031
N-methyl-N-phenylaminoacrolein
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=CC(=O)N(C)c1ccccc1
Reaction #10033
N-methyl-N-phenylaminoacrolein
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)n1c(C=CC=O)c(-c2ccc(F)cc2)c2ccccc21
Reaction #10035
product
Yield 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1c(O)ccc(C=O)c1O
Reaction #83992
product
Yield 57.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
C=CC(=O)N(C)c1ccccc1
Reaction #185600
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=Cc1ccc(C2=CCCCC2)cc1
Reaction #197394
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1cccc2[nH]cc(C=O)c12
Reaction #197672
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(-n2nc3c(cc2=O)CCCc2sc(C=O)cc2-3)cc1
Reaction #225482
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCCCCCCCCCCCCOc1ccc(C=O)s1
Reaction #249510
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CN(C=O)c1ccccc1
Reaction #251928
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1nc(OC)c(C=O)s1
Reaction #276280
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cn1ncc2c(F)c(C=O)c(F)cc21
Reaction #293782
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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