Search More · GCI-TPs

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

Precursor

FZERHIULMFGESH-UHFFFAOYSA-N

Acetanilide

C1=CC(=CC=C1)NC(C)=O

7 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

FZERHIULMFGESH-UHFFFAOYSA-N

Acetanilide

C1=CC(=CC=C1)NC(C)=O

2 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

FZERHIULMFGESH-UHFFFAOYSA-N

Acetanilide

C1=CC(=CC=C1)NC(C)=O

3 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

FZERHIULMFGESH-UHFFFAOYSA-N

Acetanilide

C1=CC(=CC=C1)NC(C)=O

4 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

FZERHIULMFGESH-UHFFFAOYSA-N

Acetanilide

C1=CC(=CC=C1)NC(C)=O

7 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

FZERHIULMFGESH-UHFFFAOYSA-N

Acetanilide

C1=CC(=CC=C1)NC(C)=O

7 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

FZERHIULMFGESH-UHFFFAOYSA-N

Acetanilide

C1=CC(=CC=C1)NC(C)=O

6 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

FZERHIULMFGESH-UHFFFAOYSA-N

Acetanilide

C1=CC(=CC=C1)NC(C)=O

10 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

FZERHIULMFGESH-UHFFFAOYSA-N

Acetanilide

C1=CC(=CC=C1)NC(C)=O

10 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

FZERHIULMFGESH-UHFFFAOYSA-N

Acetanilide

C1=CC(=CC=C1)NC(C)=O

5 steps

Dead-End Product

LJDZFAPLPVPTBD-UHFFFAOYSA-M

CID 22568690

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

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

Upstream Precursor

CYTIQZKDSHKYGB-UHFFFAOYSA-N

N-(4-Piperidinyl)phenylacetamide

CC(=O)N(C1CCNCC1)C2=CC=CC=C2

Environmental

Product

FZERHIULMFGESH-UHFFFAOYSA-N

Acetanilide

C1=CC(=CC=C1)NC(C)=O

Upstream Precursor

GGUOCFNAWIODMF-UHFFFAOYSA-N

N-(4-Chlorophenyl)acetamide

CC(Nc1ccc(cc1)Cl)=O

Abiotic

Product

FZERHIULMFGESH-UHFFFAOYSA-N

Acetanilide

C1=CC(=CC=C1)NC(C)=O

Upstream Precursor

GGUOCFNAWIODMF-UHFFFAOYSA-N

N-(4-Chlorophenyl)acetamide

CC(Nc1ccc(cc1)Cl)=O

Environmental

Product

FZERHIULMFGESH-UHFFFAOYSA-N

Acetanilide

C1=CC(=CC=C1)NC(C)=O

Upstream Precursor

HGDZGZKBJOSFHD-UHFFFAOYSA-N

C1=CC=C(C=C1)N(C2=C(C=CC=C2O)Cl)C(=O)C

Abiotic

Product

FZERHIULMFGESH-UHFFFAOYSA-N

Acetanilide

C1=CC(=CC=C1)NC(C)=O

Upstream Precursor

DLXYWZMHUVVOFZ-UHFFFAOYSA-N

N-(2-Chloro-6-nitrophenyl)-N-phenylacetamide

CC(=O)N(c1ccccc1)c2c(cccc2Cl)[N+](=O)[O-]

Abiotic

Product

FZERHIULMFGESH-UHFFFAOYSA-N

Acetanilide

C1=CC(=CC=C1)NC(C)=O

Upstream Precursor

IGXHOQNEKVKXSV-UHFFFAOYSA-N

2-(Acetylphenylamino)ethyl acetate

CC(=O)N(CCOC(=O)C)C1=CC=CC=C1

Environmental

Product

FZERHIULMFGESH-UHFFFAOYSA-N

Acetanilide

C1=CC(=CC=C1)NC(C)=O

Upstream Precursor

BIRXJKJWUZPHPJ-UHFFFAOYSA-O

4-[2-[6-(N-acetylanilino)hexa-1,3,5-trienyl]-1,1-dimethylbenzo[e]indol-3-ium-3-yl]butane-1-sulfonic acid

CC(=O)N(C=CC=CC=CC1=[N+](C2=C(C1(C)C)C3=CC=CC=C3C=C2)CCCCS(=O…

Environmental

Product

FZERHIULMFGESH-UHFFFAOYSA-N

Acetanilide

C1=CC(=CC=C1)NC(C)=O

Upstream Precursor

DKLYDESVXZKCFI-UHFFFAOYSA-N

N,N-Diphenylacetamide

CC(=O)N(C1=CC=CC=C1)C2=CC=CC=C2

Abiotic

Product

FZERHIULMFGESH-UHFFFAOYSA-N

Acetanilide

C1=CC(=CC=C1)NC(C)=O

Upstream Precursor

DEHURSMVDCYOCA-UHFFFAOYSA-N

Acetamide, N-(4,4-dicyano-1,3-butadien-1-yl)-N-phenyl-

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

Environmental

Product

FZERHIULMFGESH-UHFFFAOYSA-N

Acetanilide

C1=CC(=CC=C1)NC(C)=O

Upstream Precursor

HGMUBLQOIQNRPO-UHFFFAOYSA-O

CC[N+]1=C(SC2=CC=CC=C21)C=CC=C[NH+](C3=CC=CC=C3)C(=O)C

Environmental

Product

FZERHIULMFGESH-UHFFFAOYSA-N

Acetanilide

C1=CC(=CC=C1)NC(C)=O

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

Precursor

FZERHIULMFGESH-UHFFFAOYSA-N

Acetanilide

C1=CC(=CC=C1)NC(C)=O

Environmental

Downstream Successor

QTBSBXVTEAMEQO-UHFFFAOYSA-N

Acetic Acid

CC(=O)O

Precursor

FZERHIULMFGESH-UHFFFAOYSA-N

Acetanilide

C1=CC(=CC=C1)NC(C)=O

Abiotic

Downstream Successor

QTBSBXVTEAMEQO-UHFFFAOYSA-N

Acetic Acid

CC(=O)O

Precursor

FZERHIULMFGESH-UHFFFAOYSA-N

Acetanilide

C1=CC(=CC=C1)NC(C)=O

Environmental

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

FZERHIULMFGESH-UHFFFAOYSA-N

Acetanilide

C1=CC(=CC=C1)NC(C)=O

Environmental

Downstream Successor

PAYRUJLWNCNPSJ-UHFFFAOYSA-N

Aniline

Nc1ccccc1

Precursor

FZERHIULMFGESH-UHFFFAOYSA-N

Acetanilide

C1=CC(=CC=C1)NC(C)=O

Abiotic

Downstream Successor

PAYRUJLWNCNPSJ-UHFFFAOYSA-N

Aniline

Nc1ccccc1

Precursor

FZERHIULMFGESH-UHFFFAOYSA-N

Acetanilide

C1=CC(=CC=C1)NC(C)=O

Abiotic

Downstream Successor

AEMRFAOFKBGASW-UHFFFAOYSA-N

Glycolic Acid

C(=O)(CO)O

Precursor

FZERHIULMFGESH-UHFFFAOYSA-N

Acetanilide

C1=CC(=CC=C1)NC(C)=O

Environmental

Downstream Successor

AEMRFAOFKBGASW-UHFFFAOYSA-N

Glycolic Acid

C(=O)(CO)O

Precursor

FZERHIULMFGESH-UHFFFAOYSA-N

Acetanilide

C1=CC(=CC=C1)NC(C)=O

Environmental

Downstream Successor

DLFVBJFMPXGRIB-UHFFFAOYSA-N

Acetamide

NC(=O)C

Precursor

FZERHIULMFGESH-UHFFFAOYSA-N

Acetanilide

C1=CC(=CC=C1)NC(C)=O

Environmental

Downstream Successor

YCIMNLLNPGFGHC-UHFFFAOYSA-N

Catechol

c1c(c(ccc1)O)O

Precursor

FZERHIULMFGESH-UHFFFAOYSA-N

Acetanilide

C1=CC(=CC=C1)NC(C)=O

Abiotic

Downstream Successor

CDAWCLOXVUBKRW-UHFFFAOYSA-N

2-Aminophenol

C1=CC(=C(C=C1)O)N

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

No Original Precursors

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