ethyl cyanoacetate

CCCC(CCC)=C(C#N)C(=O)OCC
Reaction #3764
Ethyl α-cyano-α-(4-heptylidene)acetate
Ausbeute 80000.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)CC(C#N)CC#N
Reaction #40271
2-isobutyl-succinonitrile
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)C(C#N)c1ccccc1
Reaction #42163
ethyl-2-phenylcyanoacetate
Ausbeute 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)C(C#N)c1ccccc1
Reaction #42182
ethyl-2-phenylcyanoacetate
Ausbeute 53.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)C(C#N)C(=O)c1nn(-c2ccccc2)c2c1Cc1ccccc1-2
Reaction #49821
2-cyano-3-(1,4-dihydro-1-phenyl-indeno[1,2-c]pyrazol-3-yl) -3-oxo-propanoic acid, ethyl ester
Ausbeute 58.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CCOC(=O)C(C#N)CCCc1ccc(C(=O)OC)cc1
Reaction #50186
methyl 4-(4-cyano-4-ethoxycarbonylbutyl)benzoate
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CCOC(=O)c1c(N)sc(-c2ccc([N+](=O)[O-])cc2)c1C
Reaction #51529
ethyl 2-amino-4-methyl-5-(4-nitrophenyl)thiophene-3-carboxylate
Ausbeute 63.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COc1c2occc2cc2cc(C(=O)O)c(=O)oc12
Reaction #54180
7-Oxo-9-methoxy-7H-furo[3,2-g][1]benzopyran-6-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CCOC(=O)C(C#N)=C1CC(C)(C)NC(C)(C)C1
Reaction #54459
Ethyl 2,2,6,6-tetramethyl-4-piperidinylidene-cyanoacetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
COc1c2occc2cc2cc(C(=O)O)c(=O)oc12
Reaction #54653
7-Oxo-9-methoxy-7H-furo[3,2-g][1]benzopyran-6-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CCOC(=O)c1nnn(-c2ccccc2)c1N
Reaction #55964
Ethyl 5-amino-1-phenyl-1,2,3-triazole-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CCOC(=O)c1nnn(-c2ccc(C)cc2)c1N
Reaction #55967
triazole
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CCOC(=O)c1nnn(-c2ccc(Cl)cc2)c1N
Reaction #55970
triazole
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
C=CCC(C)(C)C=C(C#N)C(=O)OCC
Reaction #56713
2-Cyano-4,4-dimethyl-hepta-2,6-dienoic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCOC(=O)C(C#N)=CC1(C)CC1
Reaction #56720
ester
Ausbeute 26.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COCCCn1c(N)cc(=O)[nH]c1=S
Reaction #59339
title compound
Ausbeute 48.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Nc1cc(=O)[nH]c(=S)n1CC1CC1
Reaction #59341
title compound
Ausbeute 56.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCOC(=O)C(C#N)=Cc1cc(OC)c(OC)c2c1C=CCO2
Reaction #62747
orange solid
Ausbeute 66.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
N#Cc1cc2cccnc2nc1O
Reaction #75338
2-Hydroxy-3-cyano-1,8-naphthyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
CCOC(=O)C(C#N)c1nsc2ccc([N+](=O)[O-])cc12
Reaction #77271
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
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