Substructure Search

9130

O=C(O)CC(F)(Cl)C(F)(F)Br
Reaction #1036
4-bromo-3-chloro-3,4,4-trifiuorobutanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)([O-])[O-].[NH4+].[NH4+]
Reaction #2023
ammonium sulphate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C)cc(NC(=O)C=NO)c1
Reaction #3203
title compound
Yield 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCCN(Cc2cccc(OCCCN)c2)C1
Reaction #4745
3-[3-[(3-Methylpiperidin-1-yl)methyl]phenoxy]propanamine
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCCN(Cc2cccc(OCCCCN)c2)C1
Reaction #4746
4-[3-[(3-Methylpiperidin-1-yl)methyl]phenoxy]butanamine
DOI: 10.6084/m9.figshare.5104873.v1
OC1C2CCN(C2)C1C(O)(c1ccccc1)c1ccccc1
Reaction #5073
2-(Diphenylhydroxymethyl)-1-azabicyclo[2.2.1]heptan-3-ol
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1Cc2ccccc2N1
Reaction #6325
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(C)(C)c2cc(OCc3ccc(C=O)cc3)ccc21
Reaction #6607
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(C)(C)c2cc(OCc3ccc(CN)cc3)ccc21
Reaction #6608
4-Aminomethylbenzyl 5,6,7,8-tetrahydro-5,5,8,8-tetra-methyl-2-naphthyl ether
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NCCOc1cccc2c(S(=O)(=O)c3ccccc3F)c[nH]c12
Reaction #7052
2-[3-(2-Fluoro-benzenesulfonyl)-1H-indol-7-yloxy]-ethylamine hydrochloride
Yield 11.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCOCc1ccccc1
Reaction #7896
title compound
Yield 102.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(CC)Nc1c(CC)nn2c(-c3ccc(Cl)cc3Cl)cccc12
Reaction #9295
title compound
Yield 109.8%DOI: 10.6084/m9.figshare.5104873.v1
CC1COc2c(ccc(F)c2F)N1C(=O)C=NO
Reaction #10434
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CC#N.C=CC(=O)OCCCC
Reaction #10582
acrylonitrile n-butyl acrylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(NC2CCCC2)c(I)c1
Reaction #11512
Methyl 4-(N-cyclopentylamino)-3-iodobenzoate
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c(-c2ccccc2C(F)(F)F)nc2ncccc12
Reaction #11913
2-(2-trifluoromethyl-phenyl)-3H-pyrido[2,3-d]pyrimidin-4-one
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCNc2ccccc21
Reaction #40659
1b
Yield 93.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #42679
solid
Yield 80.0%DOI: 10.6084/m9.figshare.5104873.v1
OCc1ccc(OC(F)F)cn1
Reaction #43324
title compound
Yield 87.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(OC2CCS(=O)(=O)CC2)cc(C)c1-c1cccc(CO)c1
Reaction #43905
title compound
Yield 93.3%DOI: 10.6084/m9.figshare.5104873.v1
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