Search More · GCI-TPs

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

Precursor

HQLCHQZKYMLFKD-UHFFFAOYSA-N

(3-Methyl-1,3-thiazol-2-ylidene)-(6-phenylimidazo[2,1-b][1,3]thiazol-5-yl)iminoazanium

C[N+]1=C(SC=C1)N=NC2=C(N=C3N2C=CS3)C4=CC=CC=C4

11 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

HQLCHQZKYMLFKD-UHFFFAOYSA-N

(3-Methyl-1,3-thiazol-2-ylidene)-(6-phenylimidazo[2,1-b][1,3]thiazol-5-yl)iminoazanium

C[N+]1=C(SC=C1)N=NC2=C(N=C3N2C=CS3)C4=CC=CC=C4

2 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

HQLCHQZKYMLFKD-UHFFFAOYSA-N

(3-Methyl-1,3-thiazol-2-ylidene)-(6-phenylimidazo[2,1-b][1,3]thiazol-5-yl)iminoazanium

C[N+]1=C(SC=C1)N=NC2=C(N=C3N2C=CS3)C4=CC=CC=C4

6 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

HQLCHQZKYMLFKD-UHFFFAOYSA-N

(3-Methyl-1,3-thiazol-2-ylidene)-(6-phenylimidazo[2,1-b][1,3]thiazol-5-yl)iminoazanium

C[N+]1=C(SC=C1)N=NC2=C(N=C3N2C=CS3)C4=CC=CC=C4

7 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

HQLCHQZKYMLFKD-UHFFFAOYSA-N

(3-Methyl-1,3-thiazol-2-ylidene)-(6-phenylimidazo[2,1-b][1,3]thiazol-5-yl)iminoazanium

C[N+]1=C(SC=C1)N=NC2=C(N=C3N2C=CS3)C4=CC=CC=C4

11 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

HQLCHQZKYMLFKD-UHFFFAOYSA-N

(3-Methyl-1,3-thiazol-2-ylidene)-(6-phenylimidazo[2,1-b][1,3]thiazol-5-yl)iminoazanium

C[N+]1=C(SC=C1)N=NC2=C(N=C3N2C=CS3)C4=CC=CC=C4

11 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

HQLCHQZKYMLFKD-UHFFFAOYSA-N

(3-Methyl-1,3-thiazol-2-ylidene)-(6-phenylimidazo[2,1-b][1,3]thiazol-5-yl)iminoazanium

C[N+]1=C(SC=C1)N=NC2=C(N=C3N2C=CS3)C4=CC=CC=C4

6 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

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

Precursor

HQLCHQZKYMLFKD-UHFFFAOYSA-N

(3-Methyl-1,3-thiazol-2-ylidene)-(6-phenylimidazo[2,1-b][1,3]thiazol-5-yl)iminoazanium

C[N+]1=C(SC=C1)N=NC2=C(N=C3N2C=CS3)C4=CC=CC=C4

Abiotic

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

HQLCHQZKYMLFKD-UHFFFAOYSA-N

(3-Methyl-1,3-thiazol-2-ylidene)-(6-phenylimidazo[2,1-b][1,3]thiazol-5-yl)iminoazanium

C[N+]1=C(SC=C1)N=NC2=C(N=C3N2C=CS3)C4=CC=CC=C4

Environmental

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

HQLCHQZKYMLFKD-UHFFFAOYSA-N

(3-Methyl-1,3-thiazol-2-ylidene)-(6-phenylimidazo[2,1-b][1,3]thiazol-5-yl)iminoazanium

C[N+]1=C(SC=C1)N=NC2=C(N=C3N2C=CS3)C4=CC=CC=C4

Environmental

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

HQLCHQZKYMLFKD-UHFFFAOYSA-N

(3-Methyl-1,3-thiazol-2-ylidene)-(6-phenylimidazo[2,1-b][1,3]thiazol-5-yl)iminoazanium

C[N+]1=C(SC=C1)N=NC2=C(N=C3N2C=CS3)C4=CC=CC=C4

Environmental

Downstream Successor

JBEBGTMCZIGUTK-UHFFFAOYSA-N

2-Hydroxyhexa-2,4-diendioic acid

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

Precursor

HQLCHQZKYMLFKD-UHFFFAOYSA-N

(3-Methyl-1,3-thiazol-2-ylidene)-(6-phenylimidazo[2,1-b][1,3]thiazol-5-yl)iminoazanium

C[N+]1=C(SC=C1)N=NC2=C(N=C3N2C=CS3)C4=CC=CC=C4

Abiotic

Downstream Successor

RAIPHJJURHTUIC-UHFFFAOYSA-N

2-Aminothiazole

NC1=NC=CS1

Precursor

HQLCHQZKYMLFKD-UHFFFAOYSA-N

(3-Methyl-1,3-thiazol-2-ylidene)-(6-phenylimidazo[2,1-b][1,3]thiazol-5-yl)iminoazanium

C[N+]1=C(SC=C1)N=NC2=C(N=C3N2C=CS3)C4=CC=CC=C4

Environmental

Downstream Successor

YGUHKHFHVUKJQH-UHFFFAOYSA-O

3-Methyl-1,3-thiazol-3-ium-2-amine

NC1=[N+](C=CS1)C

Precursor

HQLCHQZKYMLFKD-UHFFFAOYSA-N

(3-Methyl-1,3-thiazol-2-ylidene)-(6-phenylimidazo[2,1-b][1,3]thiazol-5-yl)iminoazanium

C[N+]1=C(SC=C1)N=NC2=C(N=C3N2C=CS3)C4=CC=CC=C4

Abiotic

Downstream Successor

YGUHKHFHVUKJQH-UHFFFAOYSA-O

3-Methyl-1,3-thiazol-3-ium-2-amine

NC1=[N+](C=CS1)C

Precursor

HQLCHQZKYMLFKD-UHFFFAOYSA-N

(3-Methyl-1,3-thiazol-2-ylidene)-(6-phenylimidazo[2,1-b][1,3]thiazol-5-yl)iminoazanium

C[N+]1=C(SC=C1)N=NC2=C(N=C3N2C=CS3)C4=CC=CC=C4

Abiotic

Downstream Successor

YGUHKHFHVUKJQH-UHFFFAOYSA-O

3-Methyl-1,3-thiazol-3-ium-2-amine

NC1=[N+](C=CS1)C

Precursor

HQLCHQZKYMLFKD-UHFFFAOYSA-N

(3-Methyl-1,3-thiazol-2-ylidene)-(6-phenylimidazo[2,1-b][1,3]thiazol-5-yl)iminoazanium

C[N+]1=C(SC=C1)N=NC2=C(N=C3N2C=CS3)C4=CC=CC=C4

Environmental

Downstream Successor

AXYZGMCXWZBTGT-UHFFFAOYSA-N

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

Precursor

HQLCHQZKYMLFKD-UHFFFAOYSA-N

(3-Methyl-1,3-thiazol-2-ylidene)-(6-phenylimidazo[2,1-b][1,3]thiazol-5-yl)iminoazanium

C[N+]1=C(SC=C1)N=NC2=C(N=C3N2C=CS3)C4=CC=CC=C4

Abiotic

Downstream Successor

WNHAEOUPANBLKV-UHFFFAOYSA-O

C[N+]1=C(SC=C1)N=NC2=C(N=C3N2C=CS3)C4=CC=C(C(=C4)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.

No All Precursors

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

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