Search More · GCI-TPs

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

Precursor

AXQTUUPVMIBBKV-UHFFFAOYSA-N

Benzenediazonium, 2,5-dimethoxy-4-[(4-nitrophenyl)azo]-

COC1=CC(=C(C=C1N=NC2=CC=C(C=C2)[N+](=O)[O-])OC)[N+]#N

1 step

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

AXQTUUPVMIBBKV-UHFFFAOYSA-N

Benzenediazonium, 2,5-dimethoxy-4-[(4-nitrophenyl)azo]-

COC1=CC(=C(C=C1N=NC2=CC=C(C=C2)[N+](=O)[O-])OC)[N+]#N

3 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

AXQTUUPVMIBBKV-UHFFFAOYSA-N

Benzenediazonium, 2,5-dimethoxy-4-[(4-nitrophenyl)azo]-

COC1=CC(=C(C=C1N=NC2=CC=C(C=C2)[N+](=O)[O-])OC)[N+]#N

3 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

AXQTUUPVMIBBKV-UHFFFAOYSA-N

Benzenediazonium, 2,5-dimethoxy-4-[(4-nitrophenyl)azo]-

COC1=CC(=C(C=C1N=NC2=CC=C(C=C2)[N+](=O)[O-])OC)[N+]#N

8 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

AXQTUUPVMIBBKV-UHFFFAOYSA-N

Benzenediazonium, 2,5-dimethoxy-4-[(4-nitrophenyl)azo]-

COC1=CC(=C(C=C1N=NC2=CC=C(C=C2)[N+](=O)[O-])OC)[N+]#N

12 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

AXQTUUPVMIBBKV-UHFFFAOYSA-N

Benzenediazonium, 2,5-dimethoxy-4-[(4-nitrophenyl)azo]-

COC1=CC(=C(C=C1N=NC2=CC=C(C=C2)[N+](=O)[O-])OC)[N+]#N

12 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

AXQTUUPVMIBBKV-UHFFFAOYSA-N

Benzenediazonium, 2,5-dimethoxy-4-[(4-nitrophenyl)azo]-

COC1=CC(=C(C=C1N=NC2=CC=C(C=C2)[N+](=O)[O-])OC)[N+]#N

6 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

AXQTUUPVMIBBKV-UHFFFAOYSA-N

Benzenediazonium, 2,5-dimethoxy-4-[(4-nitrophenyl)azo]-

COC1=CC(=C(C=C1N=NC2=CC=C(C=C2)[N+](=O)[O-])OC)[N+]#N

16 steps

Dead-End Product

LJDZFAPLPVPTBD-UHFFFAOYSA-M

CID 22568690

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

Precursor

AXQTUUPVMIBBKV-UHFFFAOYSA-N

Benzenediazonium, 2,5-dimethoxy-4-[(4-nitrophenyl)azo]-

COC1=CC(=C(C=C1N=NC2=CC=C(C=C2)[N+](=O)[O-])OC)[N+]#N

8 steps

Dead-End Product

WCJLIWFWHPOTAC-UHFFFAOYSA-N

Rhodizonic acid

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

Precursor

AXQTUUPVMIBBKV-UHFFFAOYSA-N

Benzenediazonium, 2,5-dimethoxy-4-[(4-nitrophenyl)azo]-

COC1=CC(=C(C=C1N=NC2=CC=C(C=C2)[N+](=O)[O-])OC)[N+]#N

5 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

VTOWZOJOEIGNGU-UHFFFAOYSA-N

4-(2-(2,6-Dichloro-4-nitrophenyl)diazenyl)-2,5-dimethoxybenzenediazonium

COC1=CC(=C(C=C1N=NC2=C(C=C(C=C2Cl)[N+](=O)[O-])Cl)OC)[N+]#N

Abiotic

Product

AXQTUUPVMIBBKV-UHFFFAOYSA-N

Benzenediazonium, 2,5-dimethoxy-4-[(4-nitrophenyl)azo]-

COC1=CC(=C(C=C1N=NC2=CC=C(C=C2)[N+](=O)[O-])OC)[N+]#N

Upstream Precursor

VTOWZOJOEIGNGU-UHFFFAOYSA-N

4-(2-(2,6-Dichloro-4-nitrophenyl)diazenyl)-2,5-dimethoxybenzenediazonium

COC1=CC(=C(C=C1N=NC2=C(C=C(C=C2Cl)[N+](=O)[O-])Cl)OC)[N+]#N

Environmental

Product

AXQTUUPVMIBBKV-UHFFFAOYSA-N

Benzenediazonium, 2,5-dimethoxy-4-[(4-nitrophenyl)azo]-

COC1=CC(=C(C=C1N=NC2=CC=C(C=C2)[N+](=O)[O-])OC)[N+]#N

Upstream Precursor

NBTBILYDEZYZMQ-UHFFFAOYSA-N

COC1=CC(=C(C=C1N=NC2=C(C=C(C=C2)[N+](=O)[O-])Cl)OC)[N+]#N

Abiotic

Product

AXQTUUPVMIBBKV-UHFFFAOYSA-N

Benzenediazonium, 2,5-dimethoxy-4-[(4-nitrophenyl)azo]-

COC1=CC(=C(C=C1N=NC2=CC=C(C=C2)[N+](=O)[O-])OC)[N+]#N

Upstream Precursor

NBTBILYDEZYZMQ-UHFFFAOYSA-N

COC1=CC(=C(C=C1N=NC2=C(C=C(C=C2)[N+](=O)[O-])Cl)OC)[N+]#N

Environmental

Product

AXQTUUPVMIBBKV-UHFFFAOYSA-N

Benzenediazonium, 2,5-dimethoxy-4-[(4-nitrophenyl)azo]-

COC1=CC(=C(C=C1N=NC2=CC=C(C=C2)[N+](=O)[O-])OC)[N+]#N

Previewing top 4 entries. If you want the full results, please use the download button above.

Precursor

AXQTUUPVMIBBKV-UHFFFAOYSA-N

Benzenediazonium, 2,5-dimethoxy-4-[(4-nitrophenyl)azo]-

COC1=CC(=C(C=C1N=NC2=CC=C(C=C2)[N+](=O)[O-])OC)[N+]#N

Environmental

Downstream Successor

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

AXQTUUPVMIBBKV-UHFFFAOYSA-N

Benzenediazonium, 2,5-dimethoxy-4-[(4-nitrophenyl)azo]-

COC1=CC(=C(C=C1N=NC2=CC=C(C=C2)[N+](=O)[O-])OC)[N+]#N

Abiotic

Downstream Successor

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

AXQTUUPVMIBBKV-UHFFFAOYSA-N

Benzenediazonium, 2,5-dimethoxy-4-[(4-nitrophenyl)azo]-

COC1=CC(=C(C=C1N=NC2=CC=C(C=C2)[N+](=O)[O-])OC)[N+]#N

Abiotic

Downstream Successor

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

AXQTUUPVMIBBKV-UHFFFAOYSA-N

Benzenediazonium, 2,5-dimethoxy-4-[(4-nitrophenyl)azo]-

COC1=CC(=C(C=C1N=NC2=CC=C(C=C2)[N+](=O)[O-])OC)[N+]#N

Environmental

Downstream Successor

TYMLOMAKGOJONV-UHFFFAOYSA-N

4-Nitroaniline

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

Precursor

AXQTUUPVMIBBKV-UHFFFAOYSA-N

Benzenediazonium, 2,5-dimethoxy-4-[(4-nitrophenyl)azo]-

COC1=CC(=C(C=C1N=NC2=CC=C(C=C2)[N+](=O)[O-])OC)[N+]#N

Abiotic

Downstream Successor

TYMLOMAKGOJONV-UHFFFAOYSA-N

4-Nitroaniline

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

Precursor

AXQTUUPVMIBBKV-UHFFFAOYSA-N

Benzenediazonium, 2,5-dimethoxy-4-[(4-nitrophenyl)azo]-

COC1=CC(=C(C=C1N=NC2=CC=C(C=C2)[N+](=O)[O-])OC)[N+]#N

Abiotic

Downstream Successor

TYMLOMAKGOJONV-UHFFFAOYSA-N

4-Nitroaniline

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

Precursor

AXQTUUPVMIBBKV-UHFFFAOYSA-N

Benzenediazonium, 2,5-dimethoxy-4-[(4-nitrophenyl)azo]-

COC1=CC(=C(C=C1N=NC2=CC=C(C=C2)[N+](=O)[O-])OC)[N+]#N

Environmental

Downstream Successor

TYMLOMAKGOJONV-UHFFFAOYSA-N

4-Nitroaniline

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

Precursor

AXQTUUPVMIBBKV-UHFFFAOYSA-N

Benzenediazonium, 2,5-dimethoxy-4-[(4-nitrophenyl)azo]-

COC1=CC(=C(C=C1N=NC2=CC=C(C=C2)[N+](=O)[O-])OC)[N+]#N

Abiotic

Downstream Successor

PLIKAWJENQZMHA-UHFFFAOYSA-N

4-Aminophenol

c1cc(ccc1O)N

Precursor

AXQTUUPVMIBBKV-UHFFFAOYSA-N

Benzenediazonium, 2,5-dimethoxy-4-[(4-nitrophenyl)azo]-

COC1=CC(=C(C=C1N=NC2=CC=C(C=C2)[N+](=O)[O-])OC)[N+]#N

Environmental

Downstream Successor

PLIKAWJENQZMHA-UHFFFAOYSA-N

4-Aminophenol

c1cc(ccc1O)N

Precursor

AXQTUUPVMIBBKV-UHFFFAOYSA-N

Benzenediazonium, 2,5-dimethoxy-4-[(4-nitrophenyl)azo]-

COC1=CC(=C(C=C1N=NC2=CC=C(C=C2)[N+](=O)[O-])OC)[N+]#N

Abiotic

Downstream Successor

CBCKQZAAMUWICA-UHFFFAOYSA-N

P-Phenylenediamine

Nc1ccc(cc1)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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