Substructure Search

O=C(O)c1ccc(CBr)cc1

O=C(O)c1ccc(CBr)cc1
Reaction #1517
4-bromomethylbenzoic acid
Yield 65.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC1N=C(I)C(C=O)(Cc2ccc(C(=O)OC)c3ccccc23)N1
Reaction #2443
solid
Yield 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(CBr)c(Br)c1
Reaction #3066
ethyl 3-bromo-4-bromomethylbenzoate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(Cn2c(=O)c(-c3c(Cl)cccc3Cl)cc3cnc(N)nc32)cc1
Reaction #3325
4-[2-amino-6-(2,6-dichlorophenyl)-7-oxo-7H-pyrido[2,3-d]pyrimidin-8-ylmethyl]-benzoic acid methyl ester
Yield 70.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)cc1.[Br-]
Reaction #5148
(4-carbomethoxy)benzyltriphenylphosphonium bromide
Yield 90.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CBr)cc1
Reaction #6019
Methyl 4-(bromomethyl)benzoate
DOI: 10.6084/m9.figshare.5104873.v1
OCc1ccc(CBr)cc1
Reaction #6022
title compound
Yield 94.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1ncc(CN[C@@H](Cc2cccs2)C(=O)O)n1Cc1ccc(C(=O)O)cc1
Reaction #6583
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CN([C@@H]2CCCC[C@@H]2C(N)=O)S(=O)(=O)c2ccc(Cl)cc2)cc1
Reaction #7126
4-[[(1R,2S)-(2-carbamoyl-cyclohexyl)-(4-chlorobenzenesulfonyl)-amino]-methyl]-benzoic acid methyl ester
Yield 22.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CN([C@@H]2CCCC[C@@H]2C(N)=O)S(=O)(=O)c2ccc(Cl)cc2)cc1
Reaction #7136
titled compound
Yield 61.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CN([C@@H]2CCCCC[C@@H]2C(N)=O)S(=O)(=O)c2ccc(Cl)cc2)cc1
Reaction #7140
titled compound
Yield 28.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CN([C@@H]2CCC[C@@H]2C(N)=O)S(=O)(=O)c2ccc(Cl)cc2)cc1
Reaction #7147
titled compound
Yield 43.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(CBr)c(Cl)c1
Reaction #7834
4-(bromomethyl)-3-chlorobenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
N#CCc1ccc(C(=O)Cl)cc1Cl
Reaction #7835
3-chloro-4-(cyanomethyl)benzoyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CC#N)cc1
Reaction #9006
4-cyanomethyl-benzoic acid methyl ester
Yield 60.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CBr)c(C#N)c1
Reaction #9019
nitrile
Yield 44.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CNc2cccc3cccnc23)cc1
Reaction #11950
title compound
Yield 172.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CBr)c2ccccc12
Reaction #11954
title compound
Yield 96.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(CNc2ccccn2)c2ccccc12
Reaction #11970
title compound
Yield 9.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(CP(=O)(OC)OC)c(C(F)(F)F)c1
Reaction #42035
objective compound
DOI: 10.6084/m9.figshare.5104873.v1
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