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Depiction
Upstream Precursor
C[NH+](C)CCOC1=C(C2=C(C=CO2)C(=C1C(=O)C=CC3=CC=C(C=C3)OC)OC)OC
Depth 1
Depiction
Product
1-[6-[2-(Dimethylamino)ethoxy]-4,7-dimethoxy-1-benzofuran-5-yl]-3-(4-hydroxyphenyl)prop-2-en-1-one
CN(C)CCOC1=C(C2=C(C=CO2)C(=C1C(=O)C=CC3=CC=C(C=C3)O)OC)OC
Depiction
Upstream Precursor
C[N+](C)(CCOC1=C(C2=C(C=CO2)C(=C1C(=O)C=CC3=CC=C(C=C3)OC)OC)OC)[O-]
Depth 2
Depiction
Product
1-[6-[2-(Dimethylamino)ethoxy]-4,7-dimethoxy-1-benzofuran-5-yl]-3-(4-hydroxyphenyl)prop-2-en-1-one
CN(C)CCOC1=C(C2=C(C=CO2)C(=C1C(=O)C=CC3=CC=C(C=C3)O)OC)OC
Depiction
Upstream Precursor
CN(C)CCOC1=C(C2=C(C=CO2)C(=C1C(=O)C=CC3=CC(=C(C=C3)O)Cl)OC)OC
Depth 1
Depiction
Product
1-[6-[2-(Dimethylamino)ethoxy]-4,7-dimethoxy-1-benzofuran-5-yl]-3-(4-hydroxyphenyl)prop-2-en-1-one
CN(C)CCOC1=C(C2=C(C=CO2)C(=C1C(=O)C=CC3=CC=C(C=C3)O)OC)OC
Depiction
Upstream Precursor
C[N+](C)(CCOC1=C(C2=C(C=CO2)C(=C1C(=O)C=CC3=CC=C(C=C3)O)OC)OC)[O-]
Depth 1
Depiction
Product
1-[6-[2-(Dimethylamino)ethoxy]-4,7-dimethoxy-1-benzofuran-5-yl]-3-(4-hydroxyphenyl)prop-2-en-1-one
CN(C)CCOC1=C(C2=C(C=CO2)C(=C1C(=O)C=CC3=CC=C(C=C3)O)OC)OC
Depiction
Precursor
1-[6-[2-(Dimethylamino)ethoxy]-4,7-dimethoxy-1-benzofuran-5-yl]-3-(4-hydroxyphenyl)prop-2-en-1-one
CN(C)CCOC1=C(C2=C(C=CO2)C(=C1C(=O)C=CC3=CC=C(C=C3)O)OC)OC
Depth 2
Depiction
Downstream Successor
Formic Acid
OC=O
Depiction
Precursor
1-[6-[2-(Dimethylamino)ethoxy]-4,7-dimethoxy-1-benzofuran-5-yl]-3-(4-hydroxyphenyl)prop-2-en-1-one
CN(C)CCOC1=C(C2=C(C=CO2)C(=C1C(=O)C=CC3=CC=C(C=C3)O)OC)OC
Depth 1
Depiction
Downstream Successor
Dimethylaminium
C[NH2+]C
Depiction
Precursor
1-[6-[2-(Dimethylamino)ethoxy]-4,7-dimethoxy-1-benzofuran-5-yl]-3-(4-hydroxyphenyl)prop-2-en-1-one
CN(C)CCOC1=C(C2=C(C=CO2)C(=C1C(=O)C=CC3=CC=C(C=C3)O)OC)OC
Depth 3
Depiction
Downstream Successor
Glycolic Acid
C(=O)(CO)O
Depiction
Precursor
1-[6-[2-(Dimethylamino)ethoxy]-4,7-dimethoxy-1-benzofuran-5-yl]-3-(4-hydroxyphenyl)prop-2-en-1-one
CN(C)CCOC1=C(C2=C(C=CO2)C(=C1C(=O)C=CC3=CC=C(C=C3)O)OC)OC
Depth 2
Depiction
Downstream Successor
Glycolaldehyde
C(C=O)O
Depiction
Precursor
1-[6-[2-(Dimethylamino)ethoxy]-4,7-dimethoxy-1-benzofuran-5-yl]-3-(4-hydroxyphenyl)prop-2-en-1-one
CN(C)CCOC1=C(C2=C(C=CO2)C(=C1C(=O)C=CC3=CC=C(C=C3)O)OC)OC
Depth 3
Depiction
Downstream Successor
Glyoxylic Acid
C(=O)(C=O)O
Depiction
Precursor
1-[6-[2-(Dimethylamino)ethoxy]-4,7-dimethoxy-1-benzofuran-5-yl]-3-(4-hydroxyphenyl)prop-2-en-1-one
CN(C)CCOC1=C(C2=C(C=CO2)C(=C1C(=O)C=CC3=CC=C(C=C3)O)OC)OC
Depth 3
Depiction
Downstream Successor
Ethanolamine
NCCO
Depiction
Precursor
1-[6-[2-(Dimethylamino)ethoxy]-4,7-dimethoxy-1-benzofuran-5-yl]-3-(4-hydroxyphenyl)prop-2-en-1-one
CN(C)CCOC1=C(C2=C(C=CO2)C(=C1C(=O)C=CC3=CC=C(C=C3)O)OC)OC
Depth 2
Depiction
Downstream Successor
Dimethylhydroxylamine
N(C)(C)O
Depiction
Precursor
1-[6-[2-(Dimethylamino)ethoxy]-4,7-dimethoxy-1-benzofuran-5-yl]-3-(4-hydroxyphenyl)prop-2-en-1-one
CN(C)CCOC1=C(C2=C(C=CO2)C(=C1C(=O)C=CC3=CC=C(C=C3)O)OC)OC
Depth 3
Depiction
Downstream Successor
N-chloro-N-methylmethanamine;hydron
[NH+](C)(C)Cl
No Original Precursors

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No Dead-Ends

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