vinylpyrrolidone

C=C(C)C(=O)OCCCCCCCCCCCC.C=CN1CCCC1=O
Reaction #1498
lauryl methacrylate N-vinyl-2-pyrrolidone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #64257
polyvinyl pyrrolidone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC(CN1c2ccccc2Sc2ccccc21)N(C)C
Reaction #67390
Promethazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Fc1ccc(C2=NCCC2)c(Br)c1
Reaction #211313
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1CCCN1C1CC(CCN2CCCCC2)=NO1
Reaction #211900
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CO
Reaction #254494
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C=CN1CCCC1=O
Reaction #265736
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
C=C(c1cc2c(cc1OC)NC(=O)c1ccc(Cl)cc1N2)N1CCCC1=O
Reaction #359922
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
C=CC(=O)NCCCCCCCC.C=CC(N)=O.C=CN1CCCC1=O.CC(=O)N(C)C
Reaction #445975
N-1-Octylacrylamide Acrylamide DMA N-Vinylpyrrolidinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_03
C=CC(=O)NC(C(C)C)S(=O)(=O)[O-].C=CC(=O)NCCCCCCCC.C=CC(N)=O.C=CN1CCCC1=O.CC(=O)N(C)C.[Na+]
Reaction #445976
N-1-Octylacrylamide Acrylamide DMA N-Vinylpyrrolidinone Sodium Acrylamido-2-methylpropane sulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_03
C=CC(=O)NC(C(C)C)S(=O)(=O)[O-].C=CC(=O)NCCCCCCCCCCCCCCCC.C=CC(N)=O.C=CN1CCCC1=O.CC(=O)N(C)C.[Na+]
Reaction #445977
N-Hexadecylacrylamide Acrylamide DMA N-Vinylpyrrolidinone Sodium Acrylamido-2 -methylpropane sulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_03
C=CC(=O)NCCCCCCCC.C=CC(N)=O.C=CN1CCCC1=O.CC(=O)N(C)C
Reaction #446964
N-1-Octylacrylamide Acrylamide DMA N-Vinylpyrrolidinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_03
C=CC(=O)NC(C(C)C)S(=O)(=O)[O-].C=CC(=O)NCCCCCCCC.C=CC(N)=O.C=CN1CCCC1=O.CC(=O)N(C)C.[Na+]
Reaction #446965
N-1-Octylacrylamide Acrylamide DMA N-Vinylpyrrolidinone Sodium Acrylamido-2-methylpropane sulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_03
C=CC(=O)NC(C(C)C)S(=O)(=O)[O-].C=CC(=O)NCCCCCCCCCCCCCCCC.C=CC(N)=O.C=CN1CCCC1=O.CC(=O)N(C)C.[Na+]
Reaction #446966
N-Hexadecylacrylamide Acrylamide DMA N-Vinylpyrrolidinone Sodium Acrylamido-2-methylpropane sulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_03
C=CCOC(=O)C(=C)C
Reaction #451336
allyl methacrylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_08
C=CCOC(=O)C(=C)C
Reaction #451337
allyl methacrylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_08
C=CCOC(=O)C(=C)C
Reaction #451338
allyl methacrylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_08
C=C(C)C(=O)OCCCC
Reaction #451339
butyl methacrylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_08
C=CCOC(=O)C(=C)C
Reaction #451340
allyl methacrylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_08
C=CCOC(=O)C(=C)C
Reaction #451341
allyl methacrylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_08
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