Chlorobutyrylchloride

O=C(CCCCl)NC1CCCOc2ccccc21
Reaction #1050
5-(4-chlorobutyrylamino)-2,3,4,5-tetrahydro-1-benzoxepine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cccc(Cc2ccccc2)c1NC(=O)CCCCl
Reaction #1054
2-benzyl-1-(4-chlorobutyrylamino)-6-methylbenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(CCCCl)N1CCCOc2ccccc21
Reaction #1056
5-(4-chlorobutyryl)-2,3,4,5-tetrahydro-1,5-benzoxazepine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1ccc2[nH]cc(CCCCCl)c2c1
Reaction #5050
3-(4-chlorobutyl)-5-ethoxycarbonylindole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(CCCCl)NN=C(c1ccccc1)c1ccccc1
Reaction #8300
4-chloro-butyric acid benzhydrylidene-hydrazide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)C(=O)c1oc2nc(-c3ccc(Cl)cc3Cl)c(-c3ccc(Cl)cc3)cc2c1NC(=O)CCCCl
Reaction #8894
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc2c(=O)n(C)c(CCN3CCCC3=O)c(-c3ccccc3)c2c1
Reaction #46139
titled product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN(C)CCN1C(=O)c2cccc3cc4cccc(NC(=O)CCCCl)c4c(c23)C1=O
Reaction #46406
desired product
Yield 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)S(=O)(=O)NC1Cc2ccc(-c3cccc(CN4CCCC4=O)c3)cc2C1
Reaction #46709
title compound
Yield 19.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)c1ccc(NC(=O)CCCCl)cc1Cl
Reaction #52994
4-(4-chlorobutyryl)amino-2-chlorobenzoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Cc1coc(NC(=O)CCCCl)n1
Reaction #54763
2-(4-Chlorobutyramido)-4-methyloxazole
Yield 23.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CCCCC(C)(C)C(=O)CCCCl
Reaction #54876
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
COc1ccc(N2CCCC2=O)c(C)c1
Reaction #61067
title compound
Yield 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C(CCCCl)Nc1ccn(C(=O)CCCCl)n1
Reaction #61068
title compound
Yield 34.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CN(C(=O)CCCCl)C1CCCCC1
Reaction #63525
N-methyl-N-cyclohexyl-4-chlorobutyramide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
Cc1nnc2ccc(-c3cccc(N4CCCC4=O)c3)nn12
Reaction #63920
white crystals
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
O=C1Nc2ccccc2N(C(=O)CCCCl)c2ccccc21
Reaction #65134
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC1(C)CN(N2CCCC2=O)c2cc([N+](=O)[O-])ccc2O1
Reaction #65388
3,4-dihydro-2,2-dimethyl-4-(2-oxo-1-pyrrolidinyl)-6-nitro-2H-1,4-benzoxazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
Nc1noc(C2CN3CCC2C3)n1
Reaction #66031
oxadiazole
Yield 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCCCC(C)(C)C(=O)CCCCl
Reaction #75243
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
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