Search More · GCI-TPs

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

Precursor

UVVCYZREUQWNFB-UHFFFAOYSA-N

beta-D-Glucopyranoside, phenylmethyl 1-thio-, tetraacetate

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C

8 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

UVVCYZREUQWNFB-UHFFFAOYSA-N

beta-D-Glucopyranoside, phenylmethyl 1-thio-, tetraacetate

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C

3 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

UVVCYZREUQWNFB-UHFFFAOYSA-N

beta-D-Glucopyranoside, phenylmethyl 1-thio-, tetraacetate

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C

5 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

UVVCYZREUQWNFB-UHFFFAOYSA-N

beta-D-Glucopyranoside, phenylmethyl 1-thio-, tetraacetate

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C

4 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

UVVCYZREUQWNFB-UHFFFAOYSA-N

beta-D-Glucopyranoside, phenylmethyl 1-thio-, tetraacetate

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C

8 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

UVVCYZREUQWNFB-UHFFFAOYSA-N

beta-D-Glucopyranoside, phenylmethyl 1-thio-, tetraacetate

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C

8 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

UVVCYZREUQWNFB-UHFFFAOYSA-N

beta-D-Glucopyranoside, phenylmethyl 1-thio-, tetraacetate

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C

7 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

UVVCYZREUQWNFB-UHFFFAOYSA-N

beta-D-Glucopyranoside, phenylmethyl 1-thio-, tetraacetate

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C

12 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

UVVCYZREUQWNFB-UHFFFAOYSA-N

beta-D-Glucopyranoside, phenylmethyl 1-thio-, tetraacetate

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C

12 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

UVVCYZREUQWNFB-UHFFFAOYSA-N

beta-D-Glucopyranoside, phenylmethyl 1-thio-, tetraacetate

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C

8 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.

Upstream Precursor

UVVCYZREUQWNFB-UHFFFAOYSA-N

beta-D-Glucopyranoside, phenylmethyl 1-thio-, tetraacetate

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C

Abiotic

Product

UVVCYZREUQWNFB-UHFFFAOYSA-N

beta-D-Glucopyranoside, phenylmethyl 1-thio-, tetraacetate

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C

Upstream Precursor

UVVCYZREUQWNFB-UHFFFAOYSA-N

beta-D-Glucopyranoside, phenylmethyl 1-thio-, tetraacetate

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C

Environmental

Product

UVVCYZREUQWNFB-UHFFFAOYSA-N

beta-D-Glucopyranoside, phenylmethyl 1-thio-, tetraacetate

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C

Upstream Precursor

MGRRYYKZOYGPIR-UHFFFAOYSA-N

C(C(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C)Cl

Abiotic

Product

UVVCYZREUQWNFB-UHFFFAOYSA-N

beta-D-Glucopyranoside, phenylmethyl 1-thio-, tetraacetate

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C

Upstream Precursor

MGRRYYKZOYGPIR-UHFFFAOYSA-N

C(C(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C)Cl

Environmental

Product

UVVCYZREUQWNFB-UHFFFAOYSA-N

beta-D-Glucopyranoside, phenylmethyl 1-thio-, tetraacetate

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C

Upstream Precursor

OEJVWZRKHKQUAO-UHFFFAOYSA-N

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)CCl)OC(=O)C

Environmental

Product

UVVCYZREUQWNFB-UHFFFAOYSA-N

beta-D-Glucopyranoside, phenylmethyl 1-thio-, tetraacetate

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C

Upstream Precursor

OEJVWZRKHKQUAO-UHFFFAOYSA-N

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)CCl)OC(=O)C

Abiotic

Product

UVVCYZREUQWNFB-UHFFFAOYSA-N

beta-D-Glucopyranoside, phenylmethyl 1-thio-, tetraacetate

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C

Upstream Precursor

RNFPOJNEERBTRT-UHFFFAOYSA-N

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)CCl

Abiotic

Product

UVVCYZREUQWNFB-UHFFFAOYSA-N

beta-D-Glucopyranoside, phenylmethyl 1-thio-, tetraacetate

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C

Upstream Precursor

RNFPOJNEERBTRT-UHFFFAOYSA-N

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)CCl

Environmental

Product

UVVCYZREUQWNFB-UHFFFAOYSA-N

beta-D-Glucopyranoside, phenylmethyl 1-thio-, tetraacetate

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C

Upstream Precursor

RPQWBPGPKWWPKX-UHFFFAOYSA-N

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)CCl)OC(=O)C)OC(=O)C

Environmental

Product

UVVCYZREUQWNFB-UHFFFAOYSA-N

beta-D-Glucopyranoside, phenylmethyl 1-thio-, tetraacetate

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C

Upstream Precursor

RPQWBPGPKWWPKX-UHFFFAOYSA-N

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)CCl)OC(=O)C)OC(=O)C

Abiotic

Product

UVVCYZREUQWNFB-UHFFFAOYSA-N

beta-D-Glucopyranoside, phenylmethyl 1-thio-, tetraacetate

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C

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

Precursor

UVVCYZREUQWNFB-UHFFFAOYSA-N

beta-D-Glucopyranoside, phenylmethyl 1-thio-, tetraacetate

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C

Environmental

Downstream Successor

QTBSBXVTEAMEQO-UHFFFAOYSA-N

Acetic Acid

CC(=O)O

Precursor

UVVCYZREUQWNFB-UHFFFAOYSA-N

beta-D-Glucopyranoside, phenylmethyl 1-thio-, tetraacetate

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C

Abiotic

Downstream Successor

QTBSBXVTEAMEQO-UHFFFAOYSA-N

Acetic Acid

CC(=O)O

Precursor

UVVCYZREUQWNFB-UHFFFAOYSA-N

beta-D-Glucopyranoside, phenylmethyl 1-thio-, tetraacetate

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C

Abiotic

Downstream Successor

FOCAUTSVDIKZOP-UHFFFAOYSA-M

Chloroacetate

[O-]C(=O)CCl

Precursor

UVVCYZREUQWNFB-UHFFFAOYSA-N

beta-D-Glucopyranoside, phenylmethyl 1-thio-, tetraacetate

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C

Environmental

Downstream Successor

FOCAUTSVDIKZOP-UHFFFAOYSA-M

Chloroacetate

[O-]C(=O)CCl

Precursor

UVVCYZREUQWNFB-UHFFFAOYSA-N

beta-D-Glucopyranoside, phenylmethyl 1-thio-, tetraacetate

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C

Environmental

Downstream Successor

HUMNYLRZRPPJDN-UHFFFAOYSA-N

Benzaldehyde

c1cccc(c1)C=O

Precursor

UVVCYZREUQWNFB-UHFFFAOYSA-N

beta-D-Glucopyranoside, phenylmethyl 1-thio-, tetraacetate

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C

Environmental

Downstream Successor

AEMRFAOFKBGASW-UHFFFAOYSA-N

Glycolic Acid

C(=O)(CO)O

Precursor

UVVCYZREUQWNFB-UHFFFAOYSA-N

beta-D-Glucopyranoside, phenylmethyl 1-thio-, tetraacetate

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C

Abiotic

Downstream Successor

AEMRFAOFKBGASW-UHFFFAOYSA-N

Glycolic Acid

C(=O)(CO)O

Precursor

UVVCYZREUQWNFB-UHFFFAOYSA-N

beta-D-Glucopyranoside, phenylmethyl 1-thio-, tetraacetate

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C

Environmental

Downstream Successor

UENWRTRMUIOCKN-UHFFFAOYSA-N

Benzyl mercaptan

SCC1=CC=CC=C1

Precursor

UVVCYZREUQWNFB-UHFFFAOYSA-N

beta-D-Glucopyranoside, phenylmethyl 1-thio-, tetraacetate

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C

Environmental

Downstream Successor

IEOLRPPTIGNUNP-UHFFFAOYSA-N

GlyTouCan:G44473GG

C1(O)C(C(C(C(O1)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C

Precursor

UVVCYZREUQWNFB-UHFFFAOYSA-N

beta-D-Glucopyranoside, phenylmethyl 1-thio-, tetraacetate

CC(=O)OCC1C(C(C(C(O1)SCC2=CC=CC=C2)OC(=O)C)OC(=O)C)OC(=O)C

Environmental

Downstream Successor

BWFISYIJSZXAOV-UHFFFAOYSA-N

(3,4,5-Triacetyloxy-6-oxooxan-2-yl)methyl acetate

C1(=O)C(C(C(C(O1)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C

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.

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