Search More · GCI-TPs

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

Precursor

KDXRCOVPPZZDDV-REWJHTLYSA-N

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

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=CC=CC=C3I

1 step

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

KDXRCOVPPZZDDV-REWJHTLYSA-N

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

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=CC=CC=C3I

4 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

KDXRCOVPPZZDDV-REWJHTLYSA-N

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

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=CC=CC=C3I

7 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

KDXRCOVPPZZDDV-REWJHTLYSA-N

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

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=CC=CC=C3I

5 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

KDXRCOVPPZZDDV-REWJHTLYSA-N

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

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=CC=CC=C3I

12 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

KDXRCOVPPZZDDV-REWJHTLYSA-N

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

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=CC=CC=C3I

12 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

KDXRCOVPPZZDDV-REWJHTLYSA-N

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

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=CC=CC=C3I

7 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

KDXRCOVPPZZDDV-REWJHTLYSA-N

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

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=CC=CC=C3I

12 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

C(CC(C(O)O)O)O

Precursor

KDXRCOVPPZZDDV-REWJHTLYSA-N

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

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=CC=CC=C3I

12 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

But-1-ene-1,1,4-triol

C(CC=C(O)O)O

Precursor

KDXRCOVPPZZDDV-REWJHTLYSA-N

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

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=CC=CC=C3I

9 steps

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.

Precursor

KDXRCOVPPZZDDV-REWJHTLYSA-N

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

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=CC=CC=C3I

Environmental

Downstream Successor

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

KDXRCOVPPZZDDV-REWJHTLYSA-N

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

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=CC=CC=C3I

Abiotic

Downstream Successor

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

KDXRCOVPPZZDDV-REWJHTLYSA-N

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

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=CC=CC=C3I

Environmental

Downstream Successor

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

KDXRCOVPPZZDDV-REWJHTLYSA-N

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

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=CC=CC=C3I

Abiotic

Downstream Successor

HUMNYLRZRPPJDN-UHFFFAOYSA-N

Benzaldehyde

c1cccc(c1)C=O

Precursor

KDXRCOVPPZZDDV-REWJHTLYSA-N

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

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=CC=CC=C3I

Environmental

Downstream Successor

HUMNYLRZRPPJDN-UHFFFAOYSA-N

Benzaldehyde

c1cccc(c1)C=O

Precursor

KDXRCOVPPZZDDV-REWJHTLYSA-N

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

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=CC=CC=C3I

Environmental

Downstream Successor

WVDDGKGOMKODPV-UHFFFAOYSA-N

Benzyl Alcohol

c1cccc(c1)CO

Precursor

KDXRCOVPPZZDDV-REWJHTLYSA-N

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

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=CC=CC=C3I

Abiotic

Downstream Successor

WVDDGKGOMKODPV-UHFFFAOYSA-N

Benzyl Alcohol

c1cccc(c1)CO

Precursor

KDXRCOVPPZZDDV-REWJHTLYSA-N

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

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=CC=CC=C3I

Abiotic

Downstream Successor

KZVHICMLTWAFPI-UHFFFAOYSA-N

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

COC1CC(C2COC1O2)O

Precursor

KDXRCOVPPZZDDV-REWJHTLYSA-N

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

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=CC=CC=C3I

Environmental

Downstream Successor

KZVHICMLTWAFPI-UHFFFAOYSA-N

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

COC1CC(C2COC1O2)O

Precursor

KDXRCOVPPZZDDV-REWJHTLYSA-N

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

CO[C@@H]1C[C@@H]([C@H]2CO[C@@H]1O2)OCC3=CC=CC=C3I

Environmental

Downstream Successor

KZVHICMLTWAFPI-UHFFFAOYSA-N

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

COC1CC(C2COC1O2)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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