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Depiction
Precursor
JVOTVRCLVIKKOP-UHFFFAOYSA-N
N-[[4-[2-[4-[(hexylamino)methyl]-2-methoxyphenoxy]ethoxy]-3-methoxyphenyl]methyl]hexan-1-amine
CCCCCCNCC1=CC(=C(C=C1)OCCOC2=C(C=C(C=C2)CNCCCCCC)OC)OC
8 steps
Depiction
Dead-End Product
HEPCJCVNHBXRBO-UHFFFAOYSA-N
Succinyl-carboxylic acid
C(CCC(=O)C(=O)O)(=O)C(O)=O
Depiction
Precursor
JVOTVRCLVIKKOP-UHFFFAOYSA-N
N-[[4-[2-[4-[(hexylamino)methyl]-2-methoxyphenoxy]ethoxy]-3-methoxyphenyl]methyl]hexan-1-amine
CCCCCCNCC1=CC(=C(C=C1)OCCOC2=C(C=C(C=C2)CNCCCCCC)OC)OC
13 steps
Depiction
Dead-End Product
RBBOAWUPWQANPY-UHFFFAOYSA-N
1,2,4-Butantriol Alkohol
C(CC(C(O)O)O)O
Depiction
Precursor
JVOTVRCLVIKKOP-UHFFFAOYSA-N
N-[[4-[2-[4-[(hexylamino)methyl]-2-methoxyphenoxy]ethoxy]-3-methoxyphenyl]methyl]hexan-1-amine
CCCCCCNCC1=CC(=C(C=C1)OCCOC2=C(C=C(C=C2)CNCCCCCC)OC)OC
13 steps
Depiction
Dead-End Product
YPOPNBBFFROUGR-UHFFFAOYSA-N
But-1-ene-1,1,4-triol
C(CC=C(O)O)O
Depiction
Precursor
JVOTVRCLVIKKOP-UHFFFAOYSA-N
N-[[4-[2-[4-[(hexylamino)methyl]-2-methoxyphenoxy]ethoxy]-3-methoxyphenyl]methyl]hexan-1-amine
CCCCCCNCC1=CC(=C(C=C1)OCCOC2=C(C=C(C=C2)CNCCCCCC)OC)OC
9 steps
Depiction
Dead-End Product
WCJLIWFWHPOTAC-UHFFFAOYSA-N
Rhodizonic acid
c1(c(c(=O)c(c(c1=O)O)O)=O)=O

Previewing top 10 entries. If you want the full results, please use the download button above.

Depiction
Precursor
JVOTVRCLVIKKOP-UHFFFAOYSA-N
N-[[4-[2-[4-[(hexylamino)methyl]-2-methoxyphenoxy]ethoxy]-3-methoxyphenyl]methyl]hexan-1-amine
CCCCCCNCC1=CC(=C(C=C1)OCCOC2=C(C=C(C=C2)CNCCCCCC)OC)OC
Depth 3
Depiction
Downstream Successor
AEMRFAOFKBGASW-UHFFFAOYSA-N
Glycolic Acid
C(=O)(CO)O
Depiction
Precursor
JVOTVRCLVIKKOP-UHFFFAOYSA-N
N-[[4-[2-[4-[(hexylamino)methyl]-2-methoxyphenoxy]ethoxy]-3-methoxyphenyl]methyl]hexan-1-amine
CCCCCCNCC1=CC(=C(C=C1)OCCOC2=C(C=C(C=C2)CNCCCCCC)OC)OC
Depth 3
Depiction
Downstream Successor
HHLFWLYXYJOTON-UHFFFAOYSA-N
Glyoxylic Acid
C(=O)(C=O)O
Depiction
Precursor
JVOTVRCLVIKKOP-UHFFFAOYSA-N
N-[[4-[2-[4-[(hexylamino)methyl]-2-methoxyphenoxy]ethoxy]-3-methoxyphenyl]methyl]hexan-1-amine
CCCCCCNCC1=CC(=C(C=C1)OCCOC2=C(C=C(C=C2)CNCCCCCC)OC)OC
Depth 3
Depiction
Downstream Successor
FERIUCNNQQJTOY-UHFFFAOYSA-N
Butyric Acid
C(CCC)(O)=O
Depiction
Precursor
JVOTVRCLVIKKOP-UHFFFAOYSA-N
N-[[4-[2-[4-[(hexylamino)methyl]-2-methoxyphenoxy]ethoxy]-3-methoxyphenyl]methyl]hexan-1-amine
CCCCCCNCC1=CC(=C(C=C1)OCCOC2=C(C=C(C=C2)CNCCCCCC)OC)OC
Depth 3
Depiction
Downstream Successor
IBGBGRVKPALMCQ-UHFFFAOYSA-N
3,4-Dihydroxybenzaldehyde
Oc1c(cc(cc1)C=O)O
Depiction
Precursor
JVOTVRCLVIKKOP-UHFFFAOYSA-N
N-[[4-[2-[4-[(hexylamino)methyl]-2-methoxyphenoxy]ethoxy]-3-methoxyphenyl]methyl]hexan-1-amine
CCCCCCNCC1=CC(=C(C=C1)OCCOC2=C(C=C(C=C2)CNCCCCCC)OC)OC
Depth 3
Depiction
Downstream Successor
PCYGLFXKCBFGPC-UHFFFAOYSA-N
3,4-Dihydroxybenzyl Alcohol
OCc1cc(c(cc1)O)O

Previewing top 10 entries. If you want the full results, please use the download button above.

No Original Precursors

No entries were found for this section with the current query and depth.

No All Precursors

No entries were found for this section with the current query and depth.

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