Substructure Search

BrBr

Cn1ccc(S(=O)(=O)NC(C)(C)C)c1Br
Reaction #914
title compound
Yield 58.7%DOI: 10.6084/m9.figshare.5104873.v1
BrC1CCCCCC12OCCO2
Reaction #999
2-bromocycloheptanone ethylene ketal
DOI: 10.6084/m9.figshare.5104873.v1
Br.Cc1ccc(S(=O)(=O)Nc2ccc(NN)c(CC(C)C)c2)cc1
Reaction #1185
expected product
DOI: 10.6084/m9.figshare.5104873.v1
O=c1ccc(-c2ccc(Cl)cc2)n[nH]1
Reaction #1594
6-(4-chlorophenyl)pyridazinone
Yield 93.1%DOI: 10.6084/m9.figshare.5104873.v1
O=c1ccc(-c2ccc(Cl)cc2)n[nH]1
Reaction #1661
6-(4-chlorophenyl)pyridazinone
Yield 93.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCc1cc2c(cc1Br)CCCCC2(C)C
Reaction #1733
2-bromo-3-hexyl-5,5-dimethyl-6,7,8,9-tetrahydro-5H-benzocycloheptene
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2oc(-c3ccccc3-c3nnn[nH]3)c(Br)c2c1
Reaction #1836
product
Yield 85.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ncc(F)c(Cl)c1Br
Reaction #1956
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C#CCCCOC1CCCCO1
Reaction #2031
1-(Tetrahydopyran-2-yloxy)-4-pentyne
DOI: 10.6084/m9.figshare.5104873.v1
CC/C=C\C/C=C\CCCBr
Reaction #2033
(4Z,7Z)-1-bromo-4,7-decadiene
Yield 32.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC/C=C\CCCBr
Reaction #2039
product 17
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1ccc(-c2ccc(Cl)cc2)n[nH]1
Reaction #2166
6-(4-chlorophenyl)pyridazinone
Yield 93.1%DOI: 10.6084/m9.figshare.5104873.v1
O=c1ccc(-c2ccc(Cl)cc2)n[nH]1
Reaction #2207
6-(4-chlorophenyl)pyridazinone
Yield 93.1%DOI: 10.6084/m9.figshare.5104873.v1
O=c1ccc(-c2ccc(Cl)cc2)n[nH]1
Reaction #2266
6-(4-chlorophenyl)pyridazinone
Yield 93.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)COc1ccc(C(=O)C(C)(C)Br)cc1
Reaction #2329
methyl 4-(2-bromo-2,2-dimethylacetyl)phenoxyacetate
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncnc(OCCO)c1Br
Reaction #2410
2-(6-amino-5-bromopyrimidin-4-yloxy)ethanol
Yield 104.7%DOI: 10.6084/m9.figshare.5104873.v1
CC1Cc2cc(C(=O)O)ccc2O1
Reaction #3155
5-carboxy-2-methylcoumaran
Yield 57.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCC1Cc2cc(Br)ccc2O1
Reaction #3159
5-bromo-2-octylcoumaran
Yield 96.3%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)C(C(=O)O)n1sc2ccccc2c1=O
Reaction #3361
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@@H](C(=O)O)n1sc2ccc(F)cc2c1=O
Reaction #3362
title compound
Yield 137.3%DOI: 10.6084/m9.figshare.5104873.v1
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