Search More · GCI-TPs

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

Precursor

UDVUOKAVKXWIMC-YLFCFFPRSA-N

(1R,2S,4R,5R)-2-(cyclohexylmethoxy)-5-ethenyl-4-ethoxy-6,8-dioxabicyclo[3.2.1]octane

CCO[C@@H]1C[C@@H]([C@H]2CO[C@@]1(O2)C=C)OCC3CCCCC3

8 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

UDVUOKAVKXWIMC-YLFCFFPRSA-N

(1R,2S,4R,5R)-2-(cyclohexylmethoxy)-5-ethenyl-4-ethoxy-6,8-dioxabicyclo[3.2.1]octane

CCO[C@@H]1C[C@@H]([C@H]2CO[C@@]1(O2)C=C)OCC3CCCCC3

5 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

UDVUOKAVKXWIMC-YLFCFFPRSA-N

(1R,2S,4R,5R)-2-(cyclohexylmethoxy)-5-ethenyl-4-ethoxy-6,8-dioxabicyclo[3.2.1]octane

CCO[C@@H]1C[C@@H]([C@H]2CO[C@@]1(O2)C=C)OCC3CCCCC3

6 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

UDVUOKAVKXWIMC-YLFCFFPRSA-N

(1R,2S,4R,5R)-2-(cyclohexylmethoxy)-5-ethenyl-4-ethoxy-6,8-dioxabicyclo[3.2.1]octane

CCO[C@@H]1C[C@@H]([C@H]2CO[C@@]1(O2)C=C)OCC3CCCCC3

5 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

UDVUOKAVKXWIMC-YLFCFFPRSA-N

(1R,2S,4R,5R)-2-(cyclohexylmethoxy)-5-ethenyl-4-ethoxy-6,8-dioxabicyclo[3.2.1]octane

CCO[C@@H]1C[C@@H]([C@H]2CO[C@@]1(O2)C=C)OCC3CCCCC3

8 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

UDVUOKAVKXWIMC-YLFCFFPRSA-N

(1R,2S,4R,5R)-2-(cyclohexylmethoxy)-5-ethenyl-4-ethoxy-6,8-dioxabicyclo[3.2.1]octane

CCO[C@@H]1C[C@@H]([C@H]2CO[C@@]1(O2)C=C)OCC3CCCCC3

8 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Previewing top 6 entries. If you want the full results, please use the download button above.

Precursor

UDVUOKAVKXWIMC-YLFCFFPRSA-N

(1R,2S,4R,5R)-2-(cyclohexylmethoxy)-5-ethenyl-4-ethoxy-6,8-dioxabicyclo[3.2.1]octane

CCO[C@@H]1C[C@@H]([C@H]2CO[C@@]1(O2)C=C)OCC3CCCCC3

Environmental

Downstream Successor

QTBSBXVTEAMEQO-UHFFFAOYSA-N

Acetic Acid

CC(=O)O

Precursor

UDVUOKAVKXWIMC-YLFCFFPRSA-N

(1R,2S,4R,5R)-2-(cyclohexylmethoxy)-5-ethenyl-4-ethoxy-6,8-dioxabicyclo[3.2.1]octane

CCO[C@@H]1C[C@@H]([C@H]2CO[C@@]1(O2)C=C)OCC3CCCCC3

Environmental

Downstream Successor

IKHGUXGNUITLKF-UHFFFAOYSA-N

Acetaldehyde

C(C)=O

Precursor

UDVUOKAVKXWIMC-YLFCFFPRSA-N

(1R,2S,4R,5R)-2-(cyclohexylmethoxy)-5-ethenyl-4-ethoxy-6,8-dioxabicyclo[3.2.1]octane

CCO[C@@H]1C[C@@H]([C@H]2CO[C@@]1(O2)C=C)OCC3CCCCC3

Environmental

Downstream Successor

IKHGUXGNUITLKF-UHFFFAOYSA-N

Acetaldehyde

C(C)=O

Precursor

UDVUOKAVKXWIMC-YLFCFFPRSA-N

(1R,2S,4R,5R)-2-(cyclohexylmethoxy)-5-ethenyl-4-ethoxy-6,8-dioxabicyclo[3.2.1]octane

CCO[C@@H]1C[C@@H]([C@H]2CO[C@@]1(O2)C=C)OCC3CCCCC3

Environmental

Downstream Successor

LFQSCWFLJHTTHZ-UHFFFAOYSA-N

Ethanol

C(C)O

Precursor

UDVUOKAVKXWIMC-YLFCFFPRSA-N

(1R,2S,4R,5R)-2-(cyclohexylmethoxy)-5-ethenyl-4-ethoxy-6,8-dioxabicyclo[3.2.1]octane

CCO[C@@H]1C[C@@H]([C@H]2CO[C@@]1(O2)C=C)OCC3CCCCC3

Environmental

Downstream Successor

LFQSCWFLJHTTHZ-UHFFFAOYSA-N

Ethanol

C(C)O

Precursor

UDVUOKAVKXWIMC-YLFCFFPRSA-N

(1R,2S,4R,5R)-2-(cyclohexylmethoxy)-5-ethenyl-4-ethoxy-6,8-dioxabicyclo[3.2.1]octane

CCO[C@@H]1C[C@@H]([C@H]2CO[C@@]1(O2)C=C)OCC3CCCCC3

Environmental

Downstream Successor

AEMRFAOFKBGASW-UHFFFAOYSA-N

Glycolic Acid

C(=O)(CO)O

Precursor

UDVUOKAVKXWIMC-YLFCFFPRSA-N

(1R,2S,4R,5R)-2-(cyclohexylmethoxy)-5-ethenyl-4-ethoxy-6,8-dioxabicyclo[3.2.1]octane

CCO[C@@H]1C[C@@H]([C@H]2CO[C@@]1(O2)C=C)OCC3CCCCC3

Environmental

Downstream Successor

LYCAIKOWRPUZTN-UHFFFAOYSA-N

Ethylene Glycol

C(CO)O

Precursor

UDVUOKAVKXWIMC-YLFCFFPRSA-N

(1R,2S,4R,5R)-2-(cyclohexylmethoxy)-5-ethenyl-4-ethoxy-6,8-dioxabicyclo[3.2.1]octane

CCO[C@@H]1C[C@@H]([C@H]2CO[C@@]1(O2)C=C)OCC3CCCCC3

Environmental

Downstream Successor

QSKPIOLLBIHNAC-UHFFFAOYSA-N

Chloroacetaldehyde

O=CCCl

Precursor

UDVUOKAVKXWIMC-YLFCFFPRSA-N

(1R,2S,4R,5R)-2-(cyclohexylmethoxy)-5-ethenyl-4-ethoxy-6,8-dioxabicyclo[3.2.1]octane

CCO[C@@H]1C[C@@H]([C@H]2CO[C@@]1(O2)C=C)OCC3CCCCC3

Environmental

Downstream Successor

NZNMSOFKMUBTKW-UHFFFAOYSA-N

Cyclohexanecarboxylic acid

C1CCC(CC1)C(=O)O

Precursor

UDVUOKAVKXWIMC-YLFCFFPRSA-N

(1R,2S,4R,5R)-2-(cyclohexylmethoxy)-5-ethenyl-4-ethoxy-6,8-dioxabicyclo[3.2.1]octane

CCO[C@@H]1C[C@@H]([C@H]2CO[C@@]1(O2)C=C)OCC3CCCCC3

Environmental

Downstream Successor

KVFDZFBHBWTVID-UHFFFAOYSA-N

Cyclohexanecarboxaldehyde

C(C1CCCCC1)=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.

Search with another depth

Depth:

or Explore another compound

Higher depth reveals distant relationships but increases loading time.