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

Precursor

INECVQYBIDZALX-UHFFFAOYSA-N

4-chloro-N-(4-chloro-2-methoxy-5-methylphenyl)-3-nitrobenzamide

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)[N+](=O)[O-]

1 step

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

INECVQYBIDZALX-UHFFFAOYSA-N

4-chloro-N-(4-chloro-2-methoxy-5-methylphenyl)-3-nitrobenzamide

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)[N+](=O)[O-]

3 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

INECVQYBIDZALX-UHFFFAOYSA-N

4-chloro-N-(4-chloro-2-methoxy-5-methylphenyl)-3-nitrobenzamide

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)[N+](=O)[O-]

4 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

INECVQYBIDZALX-UHFFFAOYSA-N

4-chloro-N-(4-chloro-2-methoxy-5-methylphenyl)-3-nitrobenzamide

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)[N+](=O)[O-]

4 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

INECVQYBIDZALX-UHFFFAOYSA-N

4-chloro-N-(4-chloro-2-methoxy-5-methylphenyl)-3-nitrobenzamide

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)[N+](=O)[O-]

10 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

INECVQYBIDZALX-UHFFFAOYSA-N

4-chloro-N-(4-chloro-2-methoxy-5-methylphenyl)-3-nitrobenzamide

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)[N+](=O)[O-]

10 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

INECVQYBIDZALX-UHFFFAOYSA-N

4-chloro-N-(4-chloro-2-methoxy-5-methylphenyl)-3-nitrobenzamide

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)[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

INECVQYBIDZALX-UHFFFAOYSA-N

4-chloro-N-(4-chloro-2-methoxy-5-methylphenyl)-3-nitrobenzamide

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)[N+](=O)[O-]

12 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

INECVQYBIDZALX-UHFFFAOYSA-N

4-chloro-N-(4-chloro-2-methoxy-5-methylphenyl)-3-nitrobenzamide

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)[N+](=O)[O-]

12 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

INECVQYBIDZALX-UHFFFAOYSA-N

4-chloro-N-(4-chloro-2-methoxy-5-methylphenyl)-3-nitrobenzamide

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)[N+](=O)[O-]

4 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

PIEWZLMLTJKUCS-UHFFFAOYSA-N

3-amino-4-chloro-N-(4-chloro-2-methoxy-5-methylphenyl)benzamide

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)N

Abiotic

Product

INECVQYBIDZALX-UHFFFAOYSA-N

4-chloro-N-(4-chloro-2-methoxy-5-methylphenyl)-3-nitrobenzamide

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)[N+](=O)[O-]

Upstream Precursor

SESRMCUUIIKQIO-UHFFFAOYSA-N

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)NO

Abiotic

Product

INECVQYBIDZALX-UHFFFAOYSA-N

4-chloro-N-(4-chloro-2-methoxy-5-methylphenyl)-3-nitrobenzamide

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)[N+](=O)[O-]

Upstream Precursor

SESRMCUUIIKQIO-UHFFFAOYSA-N

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)NO

Environmental

Product

INECVQYBIDZALX-UHFFFAOYSA-N

4-chloro-N-(4-chloro-2-methoxy-5-methylphenyl)-3-nitrobenzamide

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)[N+](=O)[O-]

Upstream Precursor

SESRMCUUIIKQIO-UHFFFAOYSA-N

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)NO

Abiotic

Product

INECVQYBIDZALX-UHFFFAOYSA-N

4-chloro-N-(4-chloro-2-methoxy-5-methylphenyl)-3-nitrobenzamide

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)[N+](=O)[O-]

Upstream Precursor

FOJRZAWRYNCWRE-UHFFFAOYSA-N

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)N=O

Environmental

Product

INECVQYBIDZALX-UHFFFAOYSA-N

4-chloro-N-(4-chloro-2-methoxy-5-methylphenyl)-3-nitrobenzamide

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)[N+](=O)[O-]

Upstream Precursor

FOJRZAWRYNCWRE-UHFFFAOYSA-N

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)N=O

Abiotic

Product

INECVQYBIDZALX-UHFFFAOYSA-N

4-chloro-N-(4-chloro-2-methoxy-5-methylphenyl)-3-nitrobenzamide

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)[N+](=O)[O-]

Upstream Precursor

SVDOLRSETDPAFZ-UHFFFAOYSA-N

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)N(O)O

Abiotic

Product

INECVQYBIDZALX-UHFFFAOYSA-N

4-chloro-N-(4-chloro-2-methoxy-5-methylphenyl)-3-nitrobenzamide

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)[N+](=O)[O-]

Previewing top 7 entries. If you want the full results, please use the download button above.

Precursor

INECVQYBIDZALX-UHFFFAOYSA-N

4-chloro-N-(4-chloro-2-methoxy-5-methylphenyl)-3-nitrobenzamide

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)[N+](=O)[O-]

Abiotic

Downstream Successor

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

INECVQYBIDZALX-UHFFFAOYSA-N

4-chloro-N-(4-chloro-2-methoxy-5-methylphenyl)-3-nitrobenzamide

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)[N+](=O)[O-]

Environmental

Downstream Successor

CHFPLDURVJAORT-UHFFFAOYSA-N

4-Chloro-2,3-dihydroxybenzoic acid

c1cc(c(c(c1C(=O)O)O)O)Cl

Precursor

INECVQYBIDZALX-UHFFFAOYSA-N

4-chloro-N-(4-chloro-2-methoxy-5-methylphenyl)-3-nitrobenzamide

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)[N+](=O)[O-]

Abiotic

Downstream Successor

CHFPLDURVJAORT-UHFFFAOYSA-N

4-Chloro-2,3-dihydroxybenzoic acid

c1cc(c(c(c1C(=O)O)O)O)Cl

Precursor

INECVQYBIDZALX-UHFFFAOYSA-N

4-chloro-N-(4-chloro-2-methoxy-5-methylphenyl)-3-nitrobenzamide

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)[N+](=O)[O-]

Abiotic

Downstream Successor

DMGFVJVLVZOSOE-UHFFFAOYSA-N

3-Amino-4-chlorobenzoic acid

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

Precursor

INECVQYBIDZALX-UHFFFAOYSA-N

4-chloro-N-(4-chloro-2-methoxy-5-methylphenyl)-3-nitrobenzamide

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)[N+](=O)[O-]

Environmental

Downstream Successor

DMGFVJVLVZOSOE-UHFFFAOYSA-N

3-Amino-4-chlorobenzoic acid

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

Precursor

INECVQYBIDZALX-UHFFFAOYSA-N

4-chloro-N-(4-chloro-2-methoxy-5-methylphenyl)-3-nitrobenzamide

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)[N+](=O)[O-]

Abiotic

Downstream Successor

AFPHTEQTJZKQAQ-UHFFFAOYSA-N

3-Nitrobenzoic acid

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

Precursor

INECVQYBIDZALX-UHFFFAOYSA-N

4-chloro-N-(4-chloro-2-methoxy-5-methylphenyl)-3-nitrobenzamide

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)[N+](=O)[O-]

Environmental

Downstream Successor

AFPHTEQTJZKQAQ-UHFFFAOYSA-N

3-Nitrobenzoic acid

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

Precursor

INECVQYBIDZALX-UHFFFAOYSA-N

4-chloro-N-(4-chloro-2-methoxy-5-methylphenyl)-3-nitrobenzamide

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)[N+](=O)[O-]

Abiotic

Downstream Successor

DFXQXFGFOLXAPO-UHFFFAOYSA-N

4-Chloro-3-nitrobenzoic acid

OC(=O)c1cc(c(cc1)Cl)[N+](=O)[O-]

Precursor

INECVQYBIDZALX-UHFFFAOYSA-N

4-chloro-N-(4-chloro-2-methoxy-5-methylphenyl)-3-nitrobenzamide

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)[N+](=O)[O-]

Environmental

Downstream Successor

DFXQXFGFOLXAPO-UHFFFAOYSA-N

4-Chloro-3-nitrobenzoic acid

OC(=O)c1cc(c(cc1)Cl)[N+](=O)[O-]

Precursor

INECVQYBIDZALX-UHFFFAOYSA-N

4-chloro-N-(4-chloro-2-methoxy-5-methylphenyl)-3-nitrobenzamide

CC1=CC(=C(C=C1Cl)OC)NC(=O)C2=CC(=C(C=C2)Cl)[N+](=O)[O-]

Abiotic

Downstream Successor

DFXQXFGFOLXAPO-UHFFFAOYSA-N

4-Chloro-3-nitrobenzoic acid

OC(=O)c1cc(c(cc1)Cl)[N+](=O)[O-]

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

No Original Precursors

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