Search More · GCI-TPs

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

Precursor

JZRBCNLSIDKBMG-UHFFFAOYSA-N

1-Butyl-4-nitrobenzene

CCCCC1=CC=C(C=C1)[N+](=O)[O-]

11 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

JZRBCNLSIDKBMG-UHFFFAOYSA-N

1-Butyl-4-nitrobenzene

CCCCC1=CC=C(C=C1)[N+](=O)[O-]

2 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

JZRBCNLSIDKBMG-UHFFFAOYSA-N

1-Butyl-4-nitrobenzene

CCCCC1=CC=C(C=C1)[N+](=O)[O-]

4 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

JZRBCNLSIDKBMG-UHFFFAOYSA-N

1-Butyl-4-nitrobenzene

CCCCC1=CC=C(C=C1)[N+](=O)[O-]

7 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

JZRBCNLSIDKBMG-UHFFFAOYSA-N

1-Butyl-4-nitrobenzene

CCCCC1=CC=C(C=C1)[N+](=O)[O-]

11 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

JZRBCNLSIDKBMG-UHFFFAOYSA-N

1-Butyl-4-nitrobenzene

CCCCC1=CC=C(C=C1)[N+](=O)[O-]

11 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

JZRBCNLSIDKBMG-UHFFFAOYSA-N

1-Butyl-4-nitrobenzene

CCCCC1=CC=C(C=C1)[N+](=O)[O-]

11 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

JZRBCNLSIDKBMG-UHFFFAOYSA-N

1-Butyl-4-nitrobenzene

CCCCC1=CC=C(C=C1)[N+](=O)[O-]

17 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

JZRBCNLSIDKBMG-UHFFFAOYSA-N

1-Butyl-4-nitrobenzene

CCCCC1=CC=C(C=C1)[N+](=O)[O-]

17 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

JZRBCNLSIDKBMG-UHFFFAOYSA-N

1-Butyl-4-nitrobenzene

CCCCC1=CC=C(C=C1)[N+](=O)[O-]

9 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

OGIQUQKNJJTLSZ-UHFFFAOYSA-N

4-Butylaniline

CCCCC1=CC=C(C=C1)N

Abiotic

Product

JZRBCNLSIDKBMG-UHFFFAOYSA-N

1-Butyl-4-nitrobenzene

CCCCC1=CC=C(C=C1)[N+](=O)[O-]

Upstream Precursor

XFDALNVZYFHILZ-UHFFFAOYSA-N

1-Butyl-4-nitrosobenzene

CCCCc1ccc(cc1)N=O

Abiotic

Product

JZRBCNLSIDKBMG-UHFFFAOYSA-N

1-Butyl-4-nitrobenzene

CCCCC1=CC=C(C=C1)[N+](=O)[O-]

Upstream Precursor

FBGVWUGZXVWYLN-UHFFFAOYSA-N

Benzamide, N-(4-((4-butylphenyl)amino)-9,10-dihydro-9,10-dioxo-1-anthracenyl)-

CCCCC1=CC=C(C=C1)NC2=C3C(=C(C=C2)NC(=O)C4=CC=CC=C4)C(=O)C5=CC…

Abiotic

Product

JZRBCNLSIDKBMG-UHFFFAOYSA-N

1-Butyl-4-nitrobenzene

CCCCC1=CC=C(C=C1)[N+](=O)[O-]

Upstream Precursor

KWRCSJORDFKKLN-UHFFFAOYSA-N

N-(4-Butylphenyl)-4-[(4-chloro-2-methylphenyl)azo]-3-hydroxynaphthalene-2-carboxamide

CCCCC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=C(C=C(C=C4)Cl)C

Abiotic

Product

JZRBCNLSIDKBMG-UHFFFAOYSA-N

1-Butyl-4-nitrobenzene

CCCCC1=CC=C(C=C1)[N+](=O)[O-]

Upstream Precursor

OKWOBPOJPZEQBW-UHFFFAOYSA-N

N-(4-Butylphenyl)-4-(2-(2-chlorophenyl)diazenyl)-3-hydroxy-2-naphthalenecarboxamide

CCCCC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=CC=C4Cl

Abiotic

Product

JZRBCNLSIDKBMG-UHFFFAOYSA-N

1-Butyl-4-nitrobenzene

CCCCC1=CC=C(C=C1)[N+](=O)[O-]

Upstream Precursor

ITLXCSMSIXIRBB-UHFFFAOYSA-N

9,10-Anthracenedione, 1-[(4-butylphenyl)amino]-4-hydroxy-

CCCCC1=CC=C(C=C1)NC2=C3C(=C(C=C2)O)C(=O)C4=CC=CC=C4C3=O

Abiotic

Product

JZRBCNLSIDKBMG-UHFFFAOYSA-N

1-Butyl-4-nitrobenzene

CCCCC1=CC=C(C=C1)[N+](=O)[O-]

Upstream Precursor

FJUSLVNLSRREPY-UHFFFAOYSA-N

4-(4-Butylanilino)-3-methylphenol

CCCCC1=CC=C(C=C1)NC2=C(C=C(C=C2)O)C

Abiotic

Product

JZRBCNLSIDKBMG-UHFFFAOYSA-N

1-Butyl-4-nitrobenzene

CCCCC1=CC=C(C=C1)[N+](=O)[O-]

Upstream Precursor

RVKLSGHATZZOCO-UHFFFAOYSA-N

2-Anthracenesulfonic acid, 1-amino-4-[(4-butylphenyl)amino]-9,10-dihydro-9,10-dioxo-

CCCCC1=CC=C(C=C1)NC2=CC(=C(C3=C2C(=O)C4=CC=CC=C4C3=O)N)S(=O)(=O)O

Abiotic

Product

JZRBCNLSIDKBMG-UHFFFAOYSA-N

1-Butyl-4-nitrobenzene

CCCCC1=CC=C(C=C1)[N+](=O)[O-]

Upstream Precursor

GLFYBBZFIMBZKR-UHFFFAOYSA-N

9,10-Anthracenedione, 1-[(4-butylphenyl)amino]-

CCCCC1=CC=C(C=C1)NC2=CC=CC3=C2C(=O)C4=CC=CC=C4C3=O

Abiotic

Product

JZRBCNLSIDKBMG-UHFFFAOYSA-N

1-Butyl-4-nitrobenzene

CCCCC1=CC=C(C=C1)[N+](=O)[O-]

Upstream Precursor

QXKFNUTZQPLBMV-UHFFFAOYSA-N

6'-Diethylamino-3'-methyl-2'-(4-butylphenylamino)spiro[isobenzofuran-1(3H),9'-[9H]xanthen]-3-one

CCCCC1=CC=C(C=C1)NC2=CC3=C(C=C2C)OC4=C(C35C6=CC=CC=C6C(=O)O5)…

Abiotic

Product

JZRBCNLSIDKBMG-UHFFFAOYSA-N

1-Butyl-4-nitrobenzene

CCCCC1=CC=C(C=C1)[N+](=O)[O-]

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

Precursor

JZRBCNLSIDKBMG-UHFFFAOYSA-N

1-Butyl-4-nitrobenzene

CCCCC1=CC=C(C=C1)[N+](=O)[O-]

Environmental

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

JZRBCNLSIDKBMG-UHFFFAOYSA-N

1-Butyl-4-nitrobenzene

CCCCC1=CC=C(C=C1)[N+](=O)[O-]

Abiotic

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

JZRBCNLSIDKBMG-UHFFFAOYSA-N

1-Butyl-4-nitrobenzene

CCCCC1=CC=C(C=C1)[N+](=O)[O-]

Environmental

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

JZRBCNLSIDKBMG-UHFFFAOYSA-N

1-Butyl-4-nitrobenzene

CCCCC1=CC=C(C=C1)[N+](=O)[O-]

Environmental

Downstream Successor

NRPKPJKPJBPLIF-UHFFFAOYSA-N

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

Precursor

JZRBCNLSIDKBMG-UHFFFAOYSA-N

1-Butyl-4-nitrobenzene

CCCCC1=CC=C(C=C1)[N+](=O)[O-]

Environmental

Downstream Successor

AAKBWTHKHIMSCL-UHFFFAOYSA-N

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

Precursor

JZRBCNLSIDKBMG-UHFFFAOYSA-N

1-Butyl-4-nitrobenzene

CCCCC1=CC=C(C=C1)[N+](=O)[O-]

Environmental

Downstream Successor

CYYZDBDROVLTJU-UHFFFAOYSA-N

4-Butylphenol

CCCCc1ccc(cc1)O

Precursor

JZRBCNLSIDKBMG-UHFFFAOYSA-N

1-Butyl-4-nitrobenzene

CCCCC1=CC=C(C=C1)[N+](=O)[O-]

Abiotic

Downstream Successor

CYYZDBDROVLTJU-UHFFFAOYSA-N

4-Butylphenol

CCCCc1ccc(cc1)O

Precursor

JZRBCNLSIDKBMG-UHFFFAOYSA-N

1-Butyl-4-nitrobenzene

CCCCC1=CC=C(C=C1)[N+](=O)[O-]

Abiotic

Downstream Successor

CYYZDBDROVLTJU-UHFFFAOYSA-N

4-Butylphenol

CCCCc1ccc(cc1)O

Precursor

JZRBCNLSIDKBMG-UHFFFAOYSA-N

1-Butyl-4-nitrobenzene

CCCCC1=CC=C(C=C1)[N+](=O)[O-]

Abiotic

Downstream Successor

LAVPWYRENKSWJM-UHFFFAOYSA-N

4-Butylbenzene-1,2-diol

C1(=C(C=C(C=C1)CCCC)O)O

Precursor

JZRBCNLSIDKBMG-UHFFFAOYSA-N

1-Butyl-4-nitrobenzene

CCCCC1=CC=C(C=C1)[N+](=O)[O-]

Environmental

Downstream Successor

LAVPWYRENKSWJM-UHFFFAOYSA-N

4-Butylbenzene-1,2-diol

C1(=C(C=C(C=C1)CCCC)O)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.

Search with another depth

Depth:

or Explore another compound

Higher depth reveals distant relationships but increases loading time.