methyl 2,4-dibromobutanoate

O=C1Nc2ccccc2SC1CCBr
Reaction #322818
2-(2-bromoethyl)-2H-1,4-benzothiazin-3(4H)-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
COc1ccc2c(c1)SC(CCBr)C(=O)N2
Reaction #322819
2-(2-bromoethyl)-7-methoxy-2H-1,4-benzothiazin-3(4H)-one
Ausbeute 65.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
COC(=O)C(CCBr)Oc1ccc([N+](=O)[O-])c(F)c1
Reaction #372895
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COC(=O)C(CCBr)C(C#N)(C(=O)OC)C(C)c1ccccc1
Reaction #412950
Dimethyl 2-phenyl-3-cyano-6-bromohexane-3,4-dicarboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1984_04
CCOC(=O)C(CCCl)C(C#N)(C(=O)OCC)C(C)c1ccccc1
Reaction #412951
diethyl 2-phenyl-3-cyano-6-chlorohexane-3,4-dicarboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1984_04
COC(=O)C1(n2cc([N+](=O)[O-])cn2)CC1
Reaction #802022
title compound
Ausbeute 60.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
COC(=O)C(CCBr)SC(C)=O
Reaction #969843
title compound
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
COC(=O)C(CCBr)SC(C)=O
Reaction #969845
title compound
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
COC(=O)C(CCBr)C(C#N)(C(=O)OC)C(C)c1ccccc1
Reaction #1025020
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
CN1CCC(Br)C1=O
Reaction #1161418
3-bromo-N-methyl-2-pyrrolidone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_11
CNC(=O)C(Br)CCBr
Reaction #1161419
N-methyl-2,4-dibromobutyramide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_11
CNC(=O)C(Br)CCBr
Reaction #1161420
N-Methyl-2,4-dibromobutyramide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_11
CNC(=O)C(Br)CCBr
Reaction #1161421
N-methyl-2,4-dibromobutyramide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_11
CN1CCC(Br)C1=O
Reaction #1173963
3-bromo-N-methyl-2-pyrrolidone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_07
CNC(=O)C(Br)CCBr
Reaction #1173964
N-methyl-2,4-dibromobutyramide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_07
COC(=O)C(CCBr)Sc1cc(N)c(F)cc1Cl
Reaction #1218600
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
CNC(=O)C(Br)CCBr
Reaction #1234522
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
COC(=O)C(CCBr)Oc1ccc([N+](=O)[O-])c(F)c1
Reaction #1248532
title compound
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_10
COC(=O)C(CCBr)C(C#N)(C(=O)OC)C(C)c1ccccc1
Reaction #1335060
Dimethyl 2-phenyl-3-cyano-6-bromohexane-3,4-dicarboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_06
CCOC(=O)C(CCCl)C(C#N)(C(=O)OCC)C(C)c1ccccc1
Reaction #1335061
diethyl 2-phenyl-3-cyano-6-chlorohexane-3,4-dicarboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_06
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