Search More · GCI-TPs

Graphs show a maximum of 100 compounds. Use downloads for complete results.

Precursor

YIJLRGLWCURPOL-GBJTYRQASA-N

(1R,2S,4R,5R)-4-methoxy-2-[(2-methoxy-6-nitrophenyl)methoxy]-6,8-dioxabicyclo[3.2.1]octane

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=C(C=CC=C3OC)[N+](=O)[O-]

1 step

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

YIJLRGLWCURPOL-GBJTYRQASA-N

(1R,2S,4R,5R)-4-methoxy-2-[(2-methoxy-6-nitrophenyl)methoxy]-6,8-dioxabicyclo[3.2.1]octane

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=C(C=CC=C3OC)[N+](=O)[O-]

3 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

YIJLRGLWCURPOL-GBJTYRQASA-N

(1R,2S,4R,5R)-4-methoxy-2-[(2-methoxy-6-nitrophenyl)methoxy]-6,8-dioxabicyclo[3.2.1]octane

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=C(C=CC=C3OC)[N+](=O)[O-]

6 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

YIJLRGLWCURPOL-GBJTYRQASA-N

(1R,2S,4R,5R)-4-methoxy-2-[(2-methoxy-6-nitrophenyl)methoxy]-6,8-dioxabicyclo[3.2.1]octane

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=C(C=CC=C3OC)[N+](=O)[O-]

5 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

C(=O)(C(O)=O)O

Precursor

YIJLRGLWCURPOL-GBJTYRQASA-N

(1R,2S,4R,5R)-4-methoxy-2-[(2-methoxy-6-nitrophenyl)methoxy]-6,8-dioxabicyclo[3.2.1]octane

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=C(C=CC=C3OC)[N+](=O)[O-]

11 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

YIJLRGLWCURPOL-GBJTYRQASA-N

(1R,2S,4R,5R)-4-methoxy-2-[(2-methoxy-6-nitrophenyl)methoxy]-6,8-dioxabicyclo[3.2.1]octane

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=C(C=CC=C3OC)[N+](=O)[O-]

11 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

YIJLRGLWCURPOL-GBJTYRQASA-N

(1R,2S,4R,5R)-4-methoxy-2-[(2-methoxy-6-nitrophenyl)methoxy]-6,8-dioxabicyclo[3.2.1]octane

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=C(C=CC=C3OC)[N+](=O)[O-]

6 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

C(CCC(=O)C(=O)O)(=O)C(O)=O

Precursor

YIJLRGLWCURPOL-GBJTYRQASA-N

(1R,2S,4R,5R)-4-methoxy-2-[(2-methoxy-6-nitrophenyl)methoxy]-6,8-dioxabicyclo[3.2.1]octane

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=C(C=CC=C3OC)[N+](=O)[O-]

5 steps

Dead-End Product

LJDZFAPLPVPTBD-UHFFFAOYSA-M

CID 22568690

C([N+](=O)[O-])([O-])=O

Precursor

YIJLRGLWCURPOL-GBJTYRQASA-N

(1R,2S,4R,5R)-4-methoxy-2-[(2-methoxy-6-nitrophenyl)methoxy]-6,8-dioxabicyclo[3.2.1]octane

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=C(C=CC=C3OC)[N+](=O)[O-]

8 steps

Dead-End Product

WCJLIWFWHPOTAC-UHFFFAOYSA-N

Rhodizonic acid

c1(c(c(=O)c(c(c1=O)O)O)=O)=O

Precursor

YIJLRGLWCURPOL-GBJTYRQASA-N

(1R,2S,4R,5R)-4-methoxy-2-[(2-methoxy-6-nitrophenyl)methoxy]-6,8-dioxabicyclo[3.2.1]octane

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=C(C=CC=C3OC)[N+](=O)[O-]

8 steps

Dead-End Product

ATRULDXOZAITDR-ARJAWSKDSA-N

C(=C=C=C(O)C(=O)O)C(O)=O

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

Precursor

YIJLRGLWCURPOL-GBJTYRQASA-N

(1R,2S,4R,5R)-4-methoxy-2-[(2-methoxy-6-nitrophenyl)methoxy]-6,8-dioxabicyclo[3.2.1]octane

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=C(C=CC=C3OC)[N+](=O)[O-]

Environmental

Downstream Successor

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

YIJLRGLWCURPOL-GBJTYRQASA-N

(1R,2S,4R,5R)-4-methoxy-2-[(2-methoxy-6-nitrophenyl)methoxy]-6,8-dioxabicyclo[3.2.1]octane

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=C(C=CC=C3OC)[N+](=O)[O-]

Abiotic

Downstream Successor

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

YIJLRGLWCURPOL-GBJTYRQASA-N

(1R,2S,4R,5R)-4-methoxy-2-[(2-methoxy-6-nitrophenyl)methoxy]-6,8-dioxabicyclo[3.2.1]octane

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=C(C=CC=C3OC)[N+](=O)[O-]

Abiotic

Downstream Successor

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

YIJLRGLWCURPOL-GBJTYRQASA-N

(1R,2S,4R,5R)-4-methoxy-2-[(2-methoxy-6-nitrophenyl)methoxy]-6,8-dioxabicyclo[3.2.1]octane

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=C(C=CC=C3OC)[N+](=O)[O-]

Environmental

Downstream Successor

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

YIJLRGLWCURPOL-GBJTYRQASA-N

(1R,2S,4R,5R)-4-methoxy-2-[(2-methoxy-6-nitrophenyl)methoxy]-6,8-dioxabicyclo[3.2.1]octane

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=C(C=CC=C3OC)[N+](=O)[O-]

Environmental

Downstream Successor

KZVHICMLTWAFPI-UHFFFAOYSA-N

4-Methoxy-6,8-dioxabicyclo[3.2.1]octan-2-ol

COC1CC(C2COC1O2)O

Precursor

YIJLRGLWCURPOL-GBJTYRQASA-N

(1R,2S,4R,5R)-4-methoxy-2-[(2-methoxy-6-nitrophenyl)methoxy]-6,8-dioxabicyclo[3.2.1]octane

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=C(C=CC=C3OC)[N+](=O)[O-]

Abiotic

Downstream Successor

KZVHICMLTWAFPI-UHFFFAOYSA-N

4-Methoxy-6,8-dioxabicyclo[3.2.1]octan-2-ol

COC1CC(C2COC1O2)O

Precursor

YIJLRGLWCURPOL-GBJTYRQASA-N

(1R,2S,4R,5R)-4-methoxy-2-[(2-methoxy-6-nitrophenyl)methoxy]-6,8-dioxabicyclo[3.2.1]octane

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=C(C=CC=C3OC)[N+](=O)[O-]

Environmental

Downstream Successor

KZVHICMLTWAFPI-UHFFFAOYSA-N

4-Methoxy-6,8-dioxabicyclo[3.2.1]octan-2-ol

COC1CC(C2COC1O2)O

Precursor

YIJLRGLWCURPOL-GBJTYRQASA-N

(1R,2S,4R,5R)-4-methoxy-2-[(2-methoxy-6-nitrophenyl)methoxy]-6,8-dioxabicyclo[3.2.1]octane

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=C(C=CC=C3OC)[N+](=O)[O-]

Abiotic

Downstream Successor

BSQRUXKNBSTPCB-UHFFFAOYSA-N

4-Methoxy-6,8-dioxabicyclo[3.2.1]octan-2-one

O=C1CC(C2OCC1O2)OC

Precursor

YIJLRGLWCURPOL-GBJTYRQASA-N

(1R,2S,4R,5R)-4-methoxy-2-[(2-methoxy-6-nitrophenyl)methoxy]-6,8-dioxabicyclo[3.2.1]octane

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=C(C=CC=C3OC)[N+](=O)[O-]

Environmental

Downstream Successor

BSQRUXKNBSTPCB-UHFFFAOYSA-N

4-Methoxy-6,8-dioxabicyclo[3.2.1]octan-2-one

O=C1CC(C2OCC1O2)OC

Precursor

YIJLRGLWCURPOL-GBJTYRQASA-N

(1R,2S,4R,5R)-4-methoxy-2-[(2-methoxy-6-nitrophenyl)methoxy]-6,8-dioxabicyclo[3.2.1]octane

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=C(C=CC=C3OC)[N+](=O)[O-]

Environmental

Downstream Successor

BSQRUXKNBSTPCB-UHFFFAOYSA-N

4-Methoxy-6,8-dioxabicyclo[3.2.1]octan-2-one

O=C1CC(C2OCC1O2)OC

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.

Search with another depth

Depth:

or Explore another compound

Higher depth reveals distant relationships but increases loading time.