Search More · GCI-TPs

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

Precursor

VWPDFYRRQUHOKR-UHFFFAOYSA-N

Benzenesulfonamide, 4-methyl-N-(4-nitrophenyl)-N-(phenylmethyl)-

CC1=CC=C(C=C1)S(=O)(=O)N(CC2=CC=CC=C2)C3=CC=C(C=C3)[N+](=O)[O-]

10 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

VWPDFYRRQUHOKR-UHFFFAOYSA-N

Benzenesulfonamide, 4-methyl-N-(4-nitrophenyl)-N-(phenylmethyl)-

CC1=CC=C(C=C1)S(=O)(=O)N(CC2=CC=CC=C2)C3=CC=C(C=C3)[N+](=O)[O-]

2 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

VWPDFYRRQUHOKR-UHFFFAOYSA-N

Benzenesulfonamide, 4-methyl-N-(4-nitrophenyl)-N-(phenylmethyl)-

CC1=CC=C(C=C1)S(=O)(=O)N(CC2=CC=CC=C2)C3=CC=C(C=C3)[N+](=O)[O-]

3 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

VWPDFYRRQUHOKR-UHFFFAOYSA-N

Benzenesulfonamide, 4-methyl-N-(4-nitrophenyl)-N-(phenylmethyl)-

CC1=CC=C(C=C1)S(=O)(=O)N(CC2=CC=CC=C2)C3=CC=C(C=C3)[N+](=O)[O-]

5 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

VWPDFYRRQUHOKR-UHFFFAOYSA-N

Benzenesulfonamide, 4-methyl-N-(4-nitrophenyl)-N-(phenylmethyl)-

CC1=CC=C(C=C1)S(=O)(=O)N(CC2=CC=CC=C2)C3=CC=C(C=C3)[N+](=O)[O-]

10 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

VWPDFYRRQUHOKR-UHFFFAOYSA-N

Benzenesulfonamide, 4-methyl-N-(4-nitrophenyl)-N-(phenylmethyl)-

CC1=CC=C(C=C1)S(=O)(=O)N(CC2=CC=CC=C2)C3=CC=C(C=C3)[N+](=O)[O-]

10 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

VWPDFYRRQUHOKR-UHFFFAOYSA-N

Benzenesulfonamide, 4-methyl-N-(4-nitrophenyl)-N-(phenylmethyl)-

CC1=CC=C(C=C1)S(=O)(=O)N(CC2=CC=CC=C2)C3=CC=C(C=C3)[N+](=O)[O-]

6 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

VWPDFYRRQUHOKR-UHFFFAOYSA-N

Benzenesulfonamide, 4-methyl-N-(4-nitrophenyl)-N-(phenylmethyl)-

CC1=CC=C(C=C1)S(=O)(=O)N(CC2=CC=CC=C2)C3=CC=C(C=C3)[N+](=O)[O-]

13 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

VWPDFYRRQUHOKR-UHFFFAOYSA-N

Benzenesulfonamide, 4-methyl-N-(4-nitrophenyl)-N-(phenylmethyl)-

CC1=CC=C(C=C1)S(=O)(=O)N(CC2=CC=CC=C2)C3=CC=C(C=C3)[N+](=O)[O-]

13 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

VWPDFYRRQUHOKR-UHFFFAOYSA-N

Benzenesulfonamide, 4-methyl-N-(4-nitrophenyl)-N-(phenylmethyl)-

CC1=CC=C(C=C1)S(=O)(=O)N(CC2=CC=CC=C2)C3=CC=C(C=C3)[N+](=O)[O-]

17 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

KICSZWPFAXOJMY-UHFFFAOYSA-N

Benzenesulfonamide, N-(4-aminophenyl)-4-methyl-N-(phenylmethyl)-

CC1=CC=C(C=C1)S(=O)(=O)N(CC2=CC=CC=C2)C3=CC=C(C=C3)N

Abiotic

Product

VWPDFYRRQUHOKR-UHFFFAOYSA-N

Benzenesulfonamide, 4-methyl-N-(4-nitrophenyl)-N-(phenylmethyl)-

CC1=CC=C(C=C1)S(=O)(=O)N(CC2=CC=CC=C2)C3=CC=C(C=C3)[N+](=O)[O-]

Upstream Precursor

RZBSQQCBSKYSCN-UHFFFAOYSA-N

Cc1ccc(cc1)S(=O)(=O)N(Cc2ccccc2)c3ccc(cc3)N=O

Environmental

Product

VWPDFYRRQUHOKR-UHFFFAOYSA-N

Benzenesulfonamide, 4-methyl-N-(4-nitrophenyl)-N-(phenylmethyl)-

CC1=CC=C(C=C1)S(=O)(=O)N(CC2=CC=CC=C2)C3=CC=C(C=C3)[N+](=O)[O-]

Upstream Precursor

RZBSQQCBSKYSCN-UHFFFAOYSA-N

Cc1ccc(cc1)S(=O)(=O)N(Cc2ccccc2)c3ccc(cc3)N=O

Abiotic

Product

VWPDFYRRQUHOKR-UHFFFAOYSA-N

Benzenesulfonamide, 4-methyl-N-(4-nitrophenyl)-N-(phenylmethyl)-

CC1=CC=C(C=C1)S(=O)(=O)N(CC2=CC=CC=C2)C3=CC=C(C=C3)[N+](=O)[O-]

Upstream Precursor

ISPRNOSICCTXQO-UHFFFAOYSA-N

CC1=CC=C(C=C1)S(=O)(=O)N(CC2=CC=CC=C2)C3=CC=C(C=C3)N(O)O

Abiotic

Product

VWPDFYRRQUHOKR-UHFFFAOYSA-N

Benzenesulfonamide, 4-methyl-N-(4-nitrophenyl)-N-(phenylmethyl)-

CC1=CC=C(C=C1)S(=O)(=O)N(CC2=CC=CC=C2)C3=CC=C(C=C3)[N+](=O)[O-]

Upstream Precursor

JJAGTUSNWUVCBO-UHFFFAOYSA-N

CC1=CC=C(C=C1)S(=O)(=O)N(CC2=CC=CC=C2)C3=CC=C(C=C3)NO

Abiotic

Product

VWPDFYRRQUHOKR-UHFFFAOYSA-N

Benzenesulfonamide, 4-methyl-N-(4-nitrophenyl)-N-(phenylmethyl)-

CC1=CC=C(C=C1)S(=O)(=O)N(CC2=CC=CC=C2)C3=CC=C(C=C3)[N+](=O)[O-]

Upstream Precursor

JJAGTUSNWUVCBO-UHFFFAOYSA-N

CC1=CC=C(C=C1)S(=O)(=O)N(CC2=CC=CC=C2)C3=CC=C(C=C3)NO

Abiotic

Product

VWPDFYRRQUHOKR-UHFFFAOYSA-N

Benzenesulfonamide, 4-methyl-N-(4-nitrophenyl)-N-(phenylmethyl)-

CC1=CC=C(C=C1)S(=O)(=O)N(CC2=CC=CC=C2)C3=CC=C(C=C3)[N+](=O)[O-]

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

Precursor

VWPDFYRRQUHOKR-UHFFFAOYSA-N

Benzenesulfonamide, 4-methyl-N-(4-nitrophenyl)-N-(phenylmethyl)-

CC1=CC=C(C=C1)S(=O)(=O)N(CC2=CC=CC=C2)C3=CC=C(C=C3)[N+](=O)[O-]

Environmental

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

VWPDFYRRQUHOKR-UHFFFAOYSA-N

Benzenesulfonamide, 4-methyl-N-(4-nitrophenyl)-N-(phenylmethyl)-

CC1=CC=C(C=C1)S(=O)(=O)N(CC2=CC=CC=C2)C3=CC=C(C=C3)[N+](=O)[O-]

Abiotic

Downstream Successor

HUMNYLRZRPPJDN-UHFFFAOYSA-N

Benzaldehyde

c1cccc(c1)C=O

Precursor

VWPDFYRRQUHOKR-UHFFFAOYSA-N

Benzenesulfonamide, 4-methyl-N-(4-nitrophenyl)-N-(phenylmethyl)-

CC1=CC=C(C=C1)S(=O)(=O)N(CC2=CC=CC=C2)C3=CC=C(C=C3)[N+](=O)[O-]

Environmental

Downstream Successor

HUMNYLRZRPPJDN-UHFFFAOYSA-N

Benzaldehyde

c1cccc(c1)C=O

Precursor

VWPDFYRRQUHOKR-UHFFFAOYSA-N

Benzenesulfonamide, 4-methyl-N-(4-nitrophenyl)-N-(phenylmethyl)-

CC1=CC=C(C=C1)S(=O)(=O)N(CC2=CC=CC=C2)C3=CC=C(C=C3)[N+](=O)[O-]

Abiotic

Downstream Successor

WVDDGKGOMKODPV-UHFFFAOYSA-N

Benzyl Alcohol

c1cccc(c1)CO

Precursor

VWPDFYRRQUHOKR-UHFFFAOYSA-N

Benzenesulfonamide, 4-methyl-N-(4-nitrophenyl)-N-(phenylmethyl)-

CC1=CC=C(C=C1)S(=O)(=O)N(CC2=CC=CC=C2)C3=CC=C(C=C3)[N+](=O)[O-]

Environmental

Downstream Successor

WVDDGKGOMKODPV-UHFFFAOYSA-N

Benzyl Alcohol

c1cccc(c1)CO

Precursor

VWPDFYRRQUHOKR-UHFFFAOYSA-N

Benzenesulfonamide, 4-methyl-N-(4-nitrophenyl)-N-(phenylmethyl)-

CC1=CC=C(C=C1)S(=O)(=O)N(CC2=CC=CC=C2)C3=CC=C(C=C3)[N+](=O)[O-]

Environmental

Downstream Successor

JBEBGTMCZIGUTK-UHFFFAOYSA-N

2-Hydroxyhexa-2,4-diendioic acid

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

Precursor

VWPDFYRRQUHOKR-UHFFFAOYSA-N

Benzenesulfonamide, 4-methyl-N-(4-nitrophenyl)-N-(phenylmethyl)-

CC1=CC=C(C=C1)S(=O)(=O)N(CC2=CC=CC=C2)C3=CC=C(C=C3)[N+](=O)[O-]

Environmental

Downstream Successor

TYMLOMAKGOJONV-UHFFFAOYSA-N

4-Nitroaniline

Nc1ccc(cc1)[N+](=O)[O-]

Precursor

VWPDFYRRQUHOKR-UHFFFAOYSA-N

Benzenesulfonamide, 4-methyl-N-(4-nitrophenyl)-N-(phenylmethyl)-

CC1=CC=C(C=C1)S(=O)(=O)N(CC2=CC=CC=C2)C3=CC=C(C=C3)[N+](=O)[O-]

Abiotic

Downstream Successor

TYMLOMAKGOJONV-UHFFFAOYSA-N

4-Nitroaniline

Nc1ccc(cc1)[N+](=O)[O-]

Precursor

VWPDFYRRQUHOKR-UHFFFAOYSA-N

Benzenesulfonamide, 4-methyl-N-(4-nitrophenyl)-N-(phenylmethyl)-

CC1=CC=C(C=C1)S(=O)(=O)N(CC2=CC=CC=C2)C3=CC=C(C=C3)[N+](=O)[O-]

Environmental

Downstream Successor

JOXIMZWYDAKGHI-UHFFFAOYSA-N

p-Toluenesulfonic acid

C1=CC(=CC=C1C)S(=O)(=O)O

Precursor

VWPDFYRRQUHOKR-UHFFFAOYSA-N

Benzenesulfonamide, 4-methyl-N-(4-nitrophenyl)-N-(phenylmethyl)-

CC1=CC=C(C=C1)S(=O)(=O)N(CC2=CC=CC=C2)C3=CC=C(C=C3)[N+](=O)[O-]

Abiotic

Downstream Successor

JOXIMZWYDAKGHI-UHFFFAOYSA-N

p-Toluenesulfonic acid

C1=CC(=CC=C1C)S(=O)(=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.