Search More · GCI-TPs

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

Precursor

JNMYHXDAWVTDMS-UHFFFAOYSA-N

Benzenesulfonamide, 3-nitro-4-(phenylamino)-

C1=CC=C(C=C1)NC2=C(C=C(C=C2)S(=O)(=O)N)[N+](=O)[O-]

11 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

JNMYHXDAWVTDMS-UHFFFAOYSA-N

Benzenesulfonamide, 3-nitro-4-(phenylamino)-

C1=CC=C(C=C1)NC2=C(C=C(C=C2)S(=O)(=O)N)[N+](=O)[O-]

4 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

JNMYHXDAWVTDMS-UHFFFAOYSA-N

Benzenesulfonamide, 3-nitro-4-(phenylamino)-

C1=CC=C(C=C1)NC2=C(C=C(C=C2)S(=O)(=O)N)[N+](=O)[O-]

5 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

JNMYHXDAWVTDMS-UHFFFAOYSA-N

Benzenesulfonamide, 3-nitro-4-(phenylamino)-

C1=CC=C(C=C1)NC2=C(C=C(C=C2)S(=O)(=O)N)[N+](=O)[O-]

7 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

JNMYHXDAWVTDMS-UHFFFAOYSA-N

Benzenesulfonamide, 3-nitro-4-(phenylamino)-

C1=CC=C(C=C1)NC2=C(C=C(C=C2)S(=O)(=O)N)[N+](=O)[O-]

11 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

JNMYHXDAWVTDMS-UHFFFAOYSA-N

Benzenesulfonamide, 3-nitro-4-(phenylamino)-

C1=CC=C(C=C1)NC2=C(C=C(C=C2)S(=O)(=O)N)[N+](=O)[O-]

11 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

JNMYHXDAWVTDMS-UHFFFAOYSA-N

Benzenesulfonamide, 3-nitro-4-(phenylamino)-

C1=CC=C(C=C1)NC2=C(C=C(C=C2)S(=O)(=O)N)[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

JNMYHXDAWVTDMS-UHFFFAOYSA-N

Benzenesulfonamide, 3-nitro-4-(phenylamino)-

C1=CC=C(C=C1)NC2=C(C=C(C=C2)S(=O)(=O)N)[N+](=O)[O-]

13 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

JNMYHXDAWVTDMS-UHFFFAOYSA-N

Benzenesulfonamide, 3-nitro-4-(phenylamino)-

C1=CC=C(C=C1)NC2=C(C=C(C=C2)S(=O)(=O)N)[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

JNMYHXDAWVTDMS-UHFFFAOYSA-N

Benzenesulfonamide, 3-nitro-4-(phenylamino)-

C1=CC=C(C=C1)NC2=C(C=C(C=C2)S(=O)(=O)N)[N+](=O)[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.

Precursor

JNMYHXDAWVTDMS-UHFFFAOYSA-N

Benzenesulfonamide, 3-nitro-4-(phenylamino)-

C1=CC=C(C=C1)NC2=C(C=C(C=C2)S(=O)(=O)N)[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

JNMYHXDAWVTDMS-UHFFFAOYSA-N

Benzenesulfonamide, 3-nitro-4-(phenylamino)-

C1=CC=C(C=C1)NC2=C(C=C(C=C2)S(=O)(=O)N)[N+](=O)[O-]

Abiotic

Downstream Successor

NLRKCXQQSUWLCH-UHFFFAOYSA-N

Nitrosobenzene

C1=CC=CC=C1N=O

Precursor

JNMYHXDAWVTDMS-UHFFFAOYSA-N

Benzenesulfonamide, 3-nitro-4-(phenylamino)-

C1=CC=C(C=C1)NC2=C(C=C(C=C2)S(=O)(=O)N)[N+](=O)[O-]

Environmental

Downstream Successor

HOSFZCRSFWEDIK-UHFFFAOYSA-M

C1=C(C(=C(C=C1)NC2=C(C=C(C=C2)S(=O)(=O)[O-])[N+](=O)[O-])O)O

Precursor

JNMYHXDAWVTDMS-UHFFFAOYSA-N

Benzenesulfonamide, 3-nitro-4-(phenylamino)-

C1=CC=C(C=C1)NC2=C(C=C(C=C2)S(=O)(=O)N)[N+](=O)[O-]

Abiotic

Downstream Successor

UOQNQFOTWPZFIP-UHFFFAOYSA-N

4-Anilino-3-nitrobenzenesulfonic acid

S(=O)(=O)(C1=CC(=C(C=C1)NC2=CC=CC=C2)[N+](=O)[O-])O

Precursor

JNMYHXDAWVTDMS-UHFFFAOYSA-N

Benzenesulfonamide, 3-nitro-4-(phenylamino)-

C1=CC=C(C=C1)NC2=C(C=C(C=C2)S(=O)(=O)N)[N+](=O)[O-]

Environmental

Downstream Successor

UOQNQFOTWPZFIP-UHFFFAOYSA-N

4-Anilino-3-nitrobenzenesulfonic acid

S(=O)(=O)(C1=CC(=C(C=C1)NC2=CC=CC=C2)[N+](=O)[O-])O

Precursor

JNMYHXDAWVTDMS-UHFFFAOYSA-N

Benzenesulfonamide, 3-nitro-4-(phenylamino)-

C1=CC=C(C=C1)NC2=C(C=C(C=C2)S(=O)(=O)N)[N+](=O)[O-]

Environmental

Downstream Successor

HITNVSXPYQEDDJ-UHFFFAOYSA-N

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

Precursor

JNMYHXDAWVTDMS-UHFFFAOYSA-N

Benzenesulfonamide, 3-nitro-4-(phenylamino)-

C1=CC=C(C=C1)NC2=C(C=C(C=C2)S(=O)(=O)N)[N+](=O)[O-]

Abiotic

Downstream Successor

HITNVSXPYQEDDJ-UHFFFAOYSA-N

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

Precursor

JNMYHXDAWVTDMS-UHFFFAOYSA-N

Benzenesulfonamide, 3-nitro-4-(phenylamino)-

C1=CC=C(C=C1)NC2=C(C=C(C=C2)S(=O)(=O)N)[N+](=O)[O-]

Abiotic

Downstream Successor

ABNWONYLFMZVQN-UHFFFAOYSA-N

3-Amino-4-anilinobenzene-1-sulfonic acid

S(=O)(=O)(C1=CC(=C(C=C1)NC2=CC=CC=C2)N)O

Precursor

JNMYHXDAWVTDMS-UHFFFAOYSA-N

Benzenesulfonamide, 3-nitro-4-(phenylamino)-

C1=CC=C(C=C1)NC2=C(C=C(C=C2)S(=O)(=O)N)[N+](=O)[O-]

Environmental

Downstream Successor

ABNWONYLFMZVQN-UHFFFAOYSA-N

3-Amino-4-anilinobenzene-1-sulfonic acid

S(=O)(=O)(C1=CC(=C(C=C1)NC2=CC=CC=C2)N)O

Precursor

JNMYHXDAWVTDMS-UHFFFAOYSA-N

Benzenesulfonamide, 3-nitro-4-(phenylamino)-

C1=CC=C(C=C1)NC2=C(C=C(C=C2)S(=O)(=O)N)[N+](=O)[O-]

Abiotic

Downstream Successor

ABNWONYLFMZVQN-UHFFFAOYSA-N

3-Amino-4-anilinobenzene-1-sulfonic acid

S(=O)(=O)(C1=CC(=C(C=C1)NC2=CC=CC=C2)N)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.

No All Precursors

No entries were found for this section with the current query and depth.

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