Search More · GCI-TPs

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

Upstream Precursor

PSOVNZZNOMJUBI-UHFFFAOYSA-N

Chlorantraniliprole

CC1=CC(=CC(=C1NC(=O)C2=CC(=NN2C3=C(C=CC=N3)Cl)Br)C(=O)NC)Cl

Environmental

Product

IHHYONLRJDZQDD-UHFFFAOYSA-N

2-[[5-Bromo-2-(3-chloropyridin-2-yl)pyrazole-3-carbonyl]amino]-5-chloro-3-methylbenzoic acid

CC1=CC(=CC(=C1NC(=O)C2=CC(=NN2C3=C(C=CC=N3)Cl)Br)C(=O)O)Cl

Upstream Precursor

PSOVNZZNOMJUBI-UHFFFAOYSA-N

Chlorantraniliprole

CC1=CC(=CC(=C1NC(=O)C2=CC(=NN2C3=C(C=CC=N3)Cl)Br)C(=O)NC)Cl

Abiotic

Product

IHHYONLRJDZQDD-UHFFFAOYSA-N

2-[[5-Bromo-2-(3-chloropyridin-2-yl)pyrazole-3-carbonyl]amino]-5-chloro-3-methylbenzoic acid

CC1=CC(=CC(=C1NC(=O)C2=CC(=NN2C3=C(C=CC=N3)Cl)Br)C(=O)O)Cl

Upstream Precursor

PSOVNZZNOMJUBI-UHFFFAOYSA-N

Chlorantraniliprole

CC1=CC(=CC(=C1NC(=O)C2=CC(=NN2C3=C(C=CC=N3)Cl)Br)C(=O)NC)Cl

Environmental

Product

IHHYONLRJDZQDD-UHFFFAOYSA-N

2-[[5-Bromo-2-(3-chloropyridin-2-yl)pyrazole-3-carbonyl]amino]-5-chloro-3-methylbenzoic acid

CC1=CC(=CC(=C1NC(=O)C2=CC(=NN2C3=C(C=CC=N3)Cl)Br)C(=O)O)Cl

Upstream Precursor

YUXYKQSPWFRRSY-UHFFFAOYSA-N

N-[2-(Aminocarbonyl)-4-chloro-6-methylphenyl]-3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide

CC1=CC(=CC(=C1NC(=O)C2=CC(=NN2C3=C(C=CC=N3)Cl)Br)C(=O)N)Cl

Abiotic

Product

IHHYONLRJDZQDD-UHFFFAOYSA-N

2-[[5-Bromo-2-(3-chloropyridin-2-yl)pyrazole-3-carbonyl]amino]-5-chloro-3-methylbenzoic acid

CC1=CC(=CC(=C1NC(=O)C2=CC(=NN2C3=C(C=CC=N3)Cl)Br)C(=O)O)Cl

Upstream Precursor

YUXYKQSPWFRRSY-UHFFFAOYSA-N

N-[2-(Aminocarbonyl)-4-chloro-6-methylphenyl]-3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide

CC1=CC(=CC(=C1NC(=O)C2=CC(=NN2C3=C(C=CC=N3)Cl)Br)C(=O)N)Cl

Environmental

Product

IHHYONLRJDZQDD-UHFFFAOYSA-N

2-[[5-Bromo-2-(3-chloropyridin-2-yl)pyrazole-3-carbonyl]amino]-5-chloro-3-methylbenzoic acid

CC1=CC(=CC(=C1NC(=O)C2=CC(=NN2C3=C(C=CC=N3)Cl)Br)C(=O)O)Cl

Previewing top 5 entries. If you want the full results, please use the download button above.

Precursor

IHHYONLRJDZQDD-UHFFFAOYSA-N

2-[[5-Bromo-2-(3-chloropyridin-2-yl)pyrazole-3-carbonyl]amino]-5-chloro-3-methylbenzoic acid

CC1=CC(=CC(=C1NC(=O)C2=CC(=NN2C3=C(C=CC=N3)Cl)Br)C(=O)O)Cl

Environmental

Downstream Successor

CXNVOWPRHWWCQR-UHFFFAOYSA-N

4-Chloro-2-toluidine

CC1=C(C=CC(=C1)Cl)N

Precursor

IHHYONLRJDZQDD-UHFFFAOYSA-N

2-[[5-Bromo-2-(3-chloropyridin-2-yl)pyrazole-3-carbonyl]amino]-5-chloro-3-methylbenzoic acid

CC1=CC(=CC(=C1NC(=O)C2=CC(=NN2C3=C(C=CC=N3)Cl)Br)C(=O)O)Cl

Abiotic

Downstream Successor

CXNVOWPRHWWCQR-UHFFFAOYSA-N

4-Chloro-2-toluidine

CC1=C(C=CC(=C1)Cl)N

Precursor

IHHYONLRJDZQDD-UHFFFAOYSA-N

2-[[5-Bromo-2-(3-chloropyridin-2-yl)pyrazole-3-carbonyl]amino]-5-chloro-3-methylbenzoic acid

CC1=CC(=CC(=C1NC(=O)C2=CC(=NN2C3=C(C=CC=N3)Cl)Br)C(=O)O)Cl

Abiotic

Downstream Successor

DEMKYMVOIBWYAM-UHFFFAOYSA-N

5-Chloro-3-methyl-1,2-benzenediol

OC1=CC(=CC(=C1O)C)Cl

Precursor

IHHYONLRJDZQDD-UHFFFAOYSA-N

2-[[5-Bromo-2-(3-chloropyridin-2-yl)pyrazole-3-carbonyl]amino]-5-chloro-3-methylbenzoic acid

CC1=CC(=CC(=C1NC(=O)C2=CC(=NN2C3=C(C=CC=N3)Cl)Br)C(=O)O)Cl

Environmental

Downstream Successor

DEMKYMVOIBWYAM-UHFFFAOYSA-N

5-Chloro-3-methyl-1,2-benzenediol

OC1=CC(=CC(=C1O)C)Cl

Precursor

IHHYONLRJDZQDD-UHFFFAOYSA-N

2-[[5-Bromo-2-(3-chloropyridin-2-yl)pyrazole-3-carbonyl]amino]-5-chloro-3-methylbenzoic acid

CC1=CC(=CC(=C1NC(=O)C2=CC(=NN2C3=C(C=CC=N3)Cl)Br)C(=O)O)Cl

Environmental

Downstream Successor

DGJRAOZCJSCNGT-UHFFFAOYSA-N

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

Precursor

IHHYONLRJDZQDD-UHFFFAOYSA-N

2-[[5-Bromo-2-(3-chloropyridin-2-yl)pyrazole-3-carbonyl]amino]-5-chloro-3-methylbenzoic acid

CC1=CC(=CC(=C1NC(=O)C2=CC(=NN2C3=C(C=CC=N3)Cl)Br)C(=O)O)Cl

Abiotic

Downstream Successor

XBKOCRJFTBXJCV-UHFFFAOYSA-N

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

Precursor

IHHYONLRJDZQDD-UHFFFAOYSA-N

2-[[5-Bromo-2-(3-chloropyridin-2-yl)pyrazole-3-carbonyl]amino]-5-chloro-3-methylbenzoic acid

CC1=CC(=CC(=C1NC(=O)C2=CC(=NN2C3=C(C=CC=N3)Cl)Br)C(=O)O)Cl

Environmental

Downstream Successor

GANIICCKPXXMDW-UHFFFAOYSA-N

2-Amino-5-hydroxy-3-methylbenzoic acid

CC1=C(C(=CC(=C1)O)C(=O)O)N

Precursor

IHHYONLRJDZQDD-UHFFFAOYSA-N

2-[[5-Bromo-2-(3-chloropyridin-2-yl)pyrazole-3-carbonyl]amino]-5-chloro-3-methylbenzoic acid

CC1=CC(=CC(=C1NC(=O)C2=CC(=NN2C3=C(C=CC=N3)Cl)Br)C(=O)O)Cl

Abiotic

Downstream Successor

GANIICCKPXXMDW-UHFFFAOYSA-N

2-Amino-5-hydroxy-3-methylbenzoic acid

CC1=C(C(=CC(=C1)O)C(=O)O)N

Precursor

IHHYONLRJDZQDD-UHFFFAOYSA-N

2-[[5-Bromo-2-(3-chloropyridin-2-yl)pyrazole-3-carbonyl]amino]-5-chloro-3-methylbenzoic acid

CC1=CC(=CC(=C1NC(=O)C2=CC(=NN2C3=C(C=CC=N3)Cl)Br)C(=O)O)Cl

Abiotic

Downstream Successor

CQCSRSGYNJHRLU-UHFFFAOYSA-N

Cc1c(c(c(c(c1)Cl)O)O)N

Precursor

IHHYONLRJDZQDD-UHFFFAOYSA-N

2-[[5-Bromo-2-(3-chloropyridin-2-yl)pyrazole-3-carbonyl]amino]-5-chloro-3-methylbenzoic acid

CC1=CC(=CC(=C1NC(=O)C2=CC(=NN2C3=C(C=CC=N3)Cl)Br)C(=O)O)Cl

Environmental

Downstream Successor

CQCSRSGYNJHRLU-UHFFFAOYSA-N

Cc1c(c(c(c(c1)Cl)O)O)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.

No Dead-Ends

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

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