Substructure Search

672

CCOC(=O)c1cnc(Nc2cc(Cl)ccn2)o1
Reaction #448
Yield 0.0%
COc1c(-c2ccc3cc(NS(C)(=O)=O)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #86682
title compound
Yield 94.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(-c2ccc3cc(NS(C)(=O)=O)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #86683
Solid
Yield 167.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(-c2ccc3cc(NS(C)(=O)=O)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #86684
N-(6-(3-tert-butyl-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-2-methoxyphenyl)naphthalen-2-yl)methanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #86685
solid
Yield 89.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #86686
solid
Yield 88.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(-c2ccc3cc(NS(C)(=O)=O)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #86687
N-(6-(3-tert-butyl-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-2-methoxyphenyl)naphthalen-2-yl)methanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(-c2ccc3cc(NS(C)(=O)=O)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #86688
N-(6-(3-tert-butyl-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-2-methoxyphenyl)naphthalen-2-yl)methanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(-c2ccc3cc(NS(C)(=O)=O)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #86689
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(-c2ccc3cc(NS(C)(=O)=O)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #86690
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(OC)c(P2C(C)(C)CCCC2(C)C)c1-c1c(C(C)C)cc(C(C)C)cc1C(C)C
Reaction #166162
title compound
Yield 27.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOc1ccccc1OC
Reaction #166169
1-Butoxy-2-methoxybenzene
Yield 62.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)c1ccc([N+](=O)[O-])cc1
Reaction #166173
4-Nitrobenzophenone
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(-c2ccc3cc(NS(C)(=O)=O)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #428822
Solid
Yield 236.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2ccc(C(F)(F)F)cc2)cc1
Reaction #694823
Yield 9.0%DOI: 10.26434/chemrxiv.14388557.v1
COc1ccc(-c2c(C)cc(C)cc2C)cc1
Reaction #694913
Yield 0.0%DOI: 10.26434/chemrxiv.14388557.v1
CCOC(=O)c1ccc(-c2ccc(OC)cc2)cc1
Reaction #695003
Yield 0.0%DOI: 10.26434/chemrxiv.14388557.v1
COc1ccc(-c2ccc(C(F)(F)F)cc2)cc1
Reaction #695093
Yield 25.0%DOI: 10.26434/chemrxiv.14388557.v1
COc1ccc(-c2ccccc2)cc1
Reaction #695183
Yield 2.0%DOI: 10.26434/chemrxiv.14388557.v1
Cc1cc2c(cc(NCCO)c3nnc(C)n32)n1Cc1ccccc1
Reaction #715617
2-[(6-Benzyl-1,7-dimethyl-6H-pyrrolo[2,3-e][1,2,4]triazolo[4,3-a]pyridin-4-yl)amino]ethanol
DOI: 10.6084/m9.figshare.5104873.v1
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