Search More · GCI-TPs

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

Precursor

ODVOQTAXTDMKPZ-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-hydroxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)O)NCCC#N

8 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

ODVOQTAXTDMKPZ-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-hydroxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)O)NCCC#N

2 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

ODVOQTAXTDMKPZ-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-hydroxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)O)NCCC#N

3 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

ODVOQTAXTDMKPZ-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-hydroxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)O)NCCC#N

4 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

ODVOQTAXTDMKPZ-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-hydroxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)O)NCCC#N

8 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

ODVOQTAXTDMKPZ-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-hydroxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)O)NCCC#N

8 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

ODVOQTAXTDMKPZ-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-hydroxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)O)NCCC#N

6 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

ODVOQTAXTDMKPZ-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-hydroxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)O)NCCC#N

5 steps

Dead-End Product

LJDZFAPLPVPTBD-UHFFFAOYSA-M

CID 22568690

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

Precursor

ODVOQTAXTDMKPZ-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-hydroxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)O)NCCC#N

8 steps

Dead-End Product

WCJLIWFWHPOTAC-UHFFFAOYSA-N

Rhodizonic acid

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

Precursor

ODVOQTAXTDMKPZ-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-hydroxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)O)NCCC#N

7 steps

Dead-End Product

HJEBWCDVXVPBRC-UHFFFAOYSA-N

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

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

Upstream Precursor

ODVOQTAXTDMKPZ-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-hydroxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)O)NCCC#N

Abiotic

Product

ODVOQTAXTDMKPZ-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-hydroxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)O)NCCC#N

Upstream Precursor

OVTCINJDJPHUBX-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-methoxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)OC)NCCC#N

Abiotic

Product

ODVOQTAXTDMKPZ-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-hydroxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)O)NCCC#N

Upstream Precursor

OVTCINJDJPHUBX-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-methoxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)OC)NCCC#N

Environmental

Product

ODVOQTAXTDMKPZ-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-hydroxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)O)NCCC#N

Upstream Precursor

PJKULVBUSXRYKN-UHFFFAOYSA-N

Oc1c(cc(cc1)NC(=O)CCl)NCCC#N

Environmental

Product

ODVOQTAXTDMKPZ-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-hydroxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)O)NCCC#N

Upstream Precursor

PJKULVBUSXRYKN-UHFFFAOYSA-N

Oc1c(cc(cc1)NC(=O)CCl)NCCC#N

Abiotic

Product

ODVOQTAXTDMKPZ-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-hydroxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)O)NCCC#N

Upstream Precursor

FHJDDMLRULQBBM-UHFFFAOYSA-N

Oc1c(cc(cc1Cl)NC(=O)C)NCCC#N

Environmental

Product

ODVOQTAXTDMKPZ-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-hydroxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)O)NCCC#N

Upstream Precursor

FHJDDMLRULQBBM-UHFFFAOYSA-N

Oc1c(cc(cc1Cl)NC(=O)C)NCCC#N

Abiotic

Product

ODVOQTAXTDMKPZ-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-hydroxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)O)NCCC#N

Upstream Precursor

AXRWKWFXXNKHJP-UHFFFAOYSA-N

N-{3-[(2-Cyanoethyl)amino]-4-ethoxyphenyl}acetamide

N(CCC#N)C1=C(C=CC(=C1)NC(=O)C)OCC

Abiotic

Product

ODVOQTAXTDMKPZ-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-hydroxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)O)NCCC#N

Upstream Precursor

AXRWKWFXXNKHJP-UHFFFAOYSA-N

N-{3-[(2-Cyanoethyl)amino]-4-ethoxyphenyl}acetamide

N(CCC#N)C1=C(C=CC(=C1)NC(=O)C)OCC

Environmental

Product

ODVOQTAXTDMKPZ-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-hydroxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)O)NCCC#N

Upstream Precursor

JDOMEWCDWXXVNR-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)ethylamino]-4-ethoxyphenyl]-

CCN(CCC#N)C1=C(C=CC(=C1)NC(=O)C)OCC

Abiotic

Product

ODVOQTAXTDMKPZ-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-hydroxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)O)NCCC#N

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

Precursor

ODVOQTAXTDMKPZ-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-hydroxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)O)NCCC#N

Abiotic

Downstream Successor

QTBSBXVTEAMEQO-UHFFFAOYSA-N

Acetic Acid

CC(=O)O

Precursor

ODVOQTAXTDMKPZ-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-hydroxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)O)NCCC#N

Environmental

Downstream Successor

QTBSBXVTEAMEQO-UHFFFAOYSA-N

Acetic Acid

CC(=O)O

Precursor

ODVOQTAXTDMKPZ-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-hydroxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)O)NCCC#N

Environmental

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

ODVOQTAXTDMKPZ-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-hydroxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)O)NCCC#N

Abiotic

Downstream Successor

AEMRFAOFKBGASW-UHFFFAOYSA-N

Glycolic Acid

C(=O)(CO)O

Precursor

ODVOQTAXTDMKPZ-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-hydroxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)O)NCCC#N

Environmental

Downstream Successor

AEMRFAOFKBGASW-UHFFFAOYSA-N

Glycolic Acid

C(=O)(CO)O

Precursor

ODVOQTAXTDMKPZ-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-hydroxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)O)NCCC#N

Environmental

Downstream Successor

ZMMOYIXZGHJMNI-UHFFFAOYSA-N

Cyanoacetaldehyde

C(C#N)C=O

Precursor

ODVOQTAXTDMKPZ-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-hydroxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)O)NCCC#N

Abiotic

Downstream Successor

AGSPXMVUFBBBMO-UHFFFAOYSA-N

3-Aminopropionitrile

C(C#N)CN

Precursor

ODVOQTAXTDMKPZ-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-hydroxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)O)NCCC#N

Environmental

Downstream Successor

ZZLSKMRCEGCSIH-UHFFFAOYSA-N

Acetamide, N-(3-amino-4-hydroxyphenyl)-

Nc1c(ccc(c1)NC(=O)C)O

Precursor

ODVOQTAXTDMKPZ-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-hydroxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)O)NCCC#N

Environmental

Downstream Successor

SHIWDVVCAWWZJY-UHFFFAOYSA-N

CC(=O)NC1=CC(=C(C=C1)O)NCCC(O)=O

Precursor

ODVOQTAXTDMKPZ-UHFFFAOYSA-N

Acetamide, N-[3-[(2-cyanoethyl)amino]-4-hydroxyphenyl]-

CC(=O)NC1=CC(=C(C=C1)O)NCCC#N

Environmental

Downstream Successor

QYXHIFDZNVKEDX-UHFFFAOYSA-N

OC1=C(C=C(C=C1)N)NCCC#N

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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