chloroethane

CCC(=O)OC1(c2ccccc2)CCN(CCOC(CN(C)C(=O)OCc2ccccc2)c2ccc(Cl)c(Cl)c2)CC1.CCC(=O)OC1(c2ccccc2)CCN(CCOC(CN(C)C(=O)OCc2ccccc2)c2ccc(Cl)c(Cl)c2)CC1.Cl.Cl.O
Reaction #1937
hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)NC1(c2ccccc2)CCN(CCOC(CN(C)C(=O)OCc2ccccc2)c2ccc(Cl)c(Cl)c2)CC1.Cl
Reaction #1938
hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)NC1(c2ccccc2)CCN(CCOC(CN(C)C(=O)Cc2ccccc2)c2ccc(Cl)c(Cl)c2)CC1.CC(=O)NC1(c2ccccc2)CCN(CCOC(CN(C)C(=O)Cc2ccccc2)c2ccc(Cl)c(Cl)c2)CC1.Cl.Cl.O
Reaction #1939
hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCN(CC)C(CCOc1cccc2ccccc12)COCC
Reaction #94703
1-ethoxy-N-butyl-N-ethyl-4-(1-naphthyloxy)-2-butanamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
COc1ccc(P(=O)(Oc2ccccc2)C(=O)c2c(C)cc(C)cc2C)cc1
Reaction #191470
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCN1C(C)=C(C#N)C(c2ccc(F)c(C#N)c2)C(C#N)=C1C
Reaction #305665
1-ethyl-4-(3-cyano-4-fluorophenyl)-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarbonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CN(CC1CCN(CCCOc2ccc(F)cc2)CC1)S(=O)(=O)c1cccc2cnccc12.Cl.Cl
Reaction #335030
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
CCOP(=O)(OCC)C(=O)c1ccccc1
Reaction #380780
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOc1ccc(N)cc1
Reaction #407304
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOP(=O)(OCC)C(C)=O
Reaction #412442
diethyl acetylphosphonate
المردود 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1984_04
CCOP(=O)(OCC)C(=O)c1ccccc1
Reaction #412443
diethyl benzoylphosphonate
المردود 97.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1984_04
CCOP(=O)(OCC)C(C)=O
Reaction #416403
diethyl acetylphosphonate
المردود 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_04
CCOP(=O)(OCC)C(=O)c1ccccc1
Reaction #416404
diethyl benzoylphosphonate
المردود 97.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_04
CCON1C(=O)C2CCCCC2C1=O
Reaction #487111
N-ethoxyhexa-hydrophthalimide
المردود 79.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_10
CCON1C(=O)C2C=CCCC2C1=O
Reaction #487112
N-ethoxytetra-hydrophthalimide
المردود 74.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_10
CCON1C(=O)C2C=CCCC2C1=O
Reaction #487113
N-ethoxytetrahydrophthalimide
المردود 84.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_10
CCON1C(=O)C2C=CCCC2C1=O
Reaction #487114
N-ethoxytetrahydrophthalimide
المردود 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_10
Cl.O=C(CN1CCC(n2c(=O)[nH]c3ccccc32)CC1)c1ccc(O)c(O)c1
Reaction #531657
1-(3,4-dihydroxy phenacyl)-4-(2-oxobenzimidazolin-1-yl)piperidine hydrochloride
المردود 107.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_04
CCOP(=O)(OCC)C(OCCOc1ccc(Cl)cc1)P(=O)(OCC)OCC
Reaction #656787
Tetraethyl [2-(p-chlorophenoxy)-ethoxymethylene]-bisphosphonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_03
CCC(C#N)c1ccccc1
Reaction #684099
2-phenylbutyronitrile
المردود 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_03
الصفحة 1التالي