Search More · GCI-TPs

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

Precursor

IBCZFVVJSBMGBI-UHFFFAOYSA-N

3-Chloro-n-(4-{2-[(2-hydroxyethyl)amino]ethyl}-1,3-thiazol-2-yl)-2-methylbenzenesulfonamide

CC1=C(C=CC=C1Cl)S(=O)(=O)NC2=NC(=CS2)CCNCCO

10 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

IBCZFVVJSBMGBI-UHFFFAOYSA-N

3-Chloro-n-(4-{2-[(2-hydroxyethyl)amino]ethyl}-1,3-thiazol-2-yl)-2-methylbenzenesulfonamide

CC1=C(C=CC=C1Cl)S(=O)(=O)NC2=NC(=CS2)CCNCCO

4 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

IBCZFVVJSBMGBI-UHFFFAOYSA-N

3-Chloro-n-(4-{2-[(2-hydroxyethyl)amino]ethyl}-1,3-thiazol-2-yl)-2-methylbenzenesulfonamide

CC1=C(C=CC=C1Cl)S(=O)(=O)NC2=NC(=CS2)CCNCCO

7 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

IBCZFVVJSBMGBI-UHFFFAOYSA-N

3-Chloro-n-(4-{2-[(2-hydroxyethyl)amino]ethyl}-1,3-thiazol-2-yl)-2-methylbenzenesulfonamide

CC1=C(C=CC=C1Cl)S(=O)(=O)NC2=NC(=CS2)CCNCCO

4 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

IBCZFVVJSBMGBI-UHFFFAOYSA-N

3-Chloro-n-(4-{2-[(2-hydroxyethyl)amino]ethyl}-1,3-thiazol-2-yl)-2-methylbenzenesulfonamide

CC1=C(C=CC=C1Cl)S(=O)(=O)NC2=NC(=CS2)CCNCCO

10 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

IBCZFVVJSBMGBI-UHFFFAOYSA-N

3-Chloro-n-(4-{2-[(2-hydroxyethyl)amino]ethyl}-1,3-thiazol-2-yl)-2-methylbenzenesulfonamide

CC1=C(C=CC=C1Cl)S(=O)(=O)NC2=NC(=CS2)CCNCCO

10 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

IBCZFVVJSBMGBI-UHFFFAOYSA-N

3-Chloro-n-(4-{2-[(2-hydroxyethyl)amino]ethyl}-1,3-thiazol-2-yl)-2-methylbenzenesulfonamide

CC1=C(C=CC=C1Cl)S(=O)(=O)NC2=NC(=CS2)CCNCCO

6 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

IBCZFVVJSBMGBI-UHFFFAOYSA-N

3-Chloro-n-(4-{2-[(2-hydroxyethyl)amino]ethyl}-1,3-thiazol-2-yl)-2-methylbenzenesulfonamide

CC1=C(C=CC=C1Cl)S(=O)(=O)NC2=NC(=CS2)CCNCCO

11 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

IBCZFVVJSBMGBI-UHFFFAOYSA-N

3-Chloro-n-(4-{2-[(2-hydroxyethyl)amino]ethyl}-1,3-thiazol-2-yl)-2-methylbenzenesulfonamide

CC1=C(C=CC=C1Cl)S(=O)(=O)NC2=NC(=CS2)CCNCCO

11 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

IBCZFVVJSBMGBI-UHFFFAOYSA-N

3-Chloro-n-(4-{2-[(2-hydroxyethyl)amino]ethyl}-1,3-thiazol-2-yl)-2-methylbenzenesulfonamide

CC1=C(C=CC=C1Cl)S(=O)(=O)NC2=NC(=CS2)CCNCCO

10 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

IBCZFVVJSBMGBI-UHFFFAOYSA-N

3-Chloro-n-(4-{2-[(2-hydroxyethyl)amino]ethyl}-1,3-thiazol-2-yl)-2-methylbenzenesulfonamide

CC1=C(C=CC=C1Cl)S(=O)(=O)NC2=NC(=CS2)CCNCCO

Environmental

Downstream Successor

AEMRFAOFKBGASW-UHFFFAOYSA-N

Glycolic Acid

C(=O)(CO)O

Precursor

IBCZFVVJSBMGBI-UHFFFAOYSA-N

3-Chloro-n-(4-{2-[(2-hydroxyethyl)amino]ethyl}-1,3-thiazol-2-yl)-2-methylbenzenesulfonamide

CC1=C(C=CC=C1Cl)S(=O)(=O)NC2=NC(=CS2)CCNCCO

Environmental

Downstream Successor

WGCNASOHLSPBMP-UHFFFAOYSA-N

Glycolaldehyde

C(C=O)O

Precursor

IBCZFVVJSBMGBI-UHFFFAOYSA-N

3-Chloro-n-(4-{2-[(2-hydroxyethyl)amino]ethyl}-1,3-thiazol-2-yl)-2-methylbenzenesulfonamide

CC1=C(C=CC=C1Cl)S(=O)(=O)NC2=NC(=CS2)CCNCCO

Environmental

Downstream Successor

HZAXFHJVJLSVMW-UHFFFAOYSA-N

Ethanolamine

NCCO

Precursor

IBCZFVVJSBMGBI-UHFFFAOYSA-N

3-Chloro-n-(4-{2-[(2-hydroxyethyl)amino]ethyl}-1,3-thiazol-2-yl)-2-methylbenzenesulfonamide

CC1=C(C=CC=C1Cl)S(=O)(=O)NC2=NC(=CS2)CCNCCO

Abiotic

Downstream Successor

HZAXFHJVJLSVMW-UHFFFAOYSA-N

Ethanolamine

NCCO

Precursor

IBCZFVVJSBMGBI-UHFFFAOYSA-N

3-Chloro-n-(4-{2-[(2-hydroxyethyl)amino]ethyl}-1,3-thiazol-2-yl)-2-methylbenzenesulfonamide

CC1=C(C=CC=C1Cl)S(=O)(=O)NC2=NC(=CS2)CCNCCO

Environmental

Downstream Successor

HZAXFHJVJLSVMW-UHFFFAOYSA-N

Ethanolamine

NCCO

Precursor

IBCZFVVJSBMGBI-UHFFFAOYSA-N

3-Chloro-n-(4-{2-[(2-hydroxyethyl)amino]ethyl}-1,3-thiazol-2-yl)-2-methylbenzenesulfonamide

CC1=C(C=CC=C1Cl)S(=O)(=O)NC2=NC(=CS2)CCNCCO

Environmental

Downstream Successor

LYIIBVSRGJSHAV-UHFFFAOYSA-N

Aminoacetaldehyde

NCC=O

Precursor

IBCZFVVJSBMGBI-UHFFFAOYSA-N

3-Chloro-n-(4-{2-[(2-hydroxyethyl)amino]ethyl}-1,3-thiazol-2-yl)-2-methylbenzenesulfonamide

CC1=C(C=CC=C1Cl)S(=O)(=O)NC2=NC(=CS2)CCNCCO

Abiotic

Downstream Successor

QWVGKYWNOKOFNN-UHFFFAOYSA-N

O-Cresol

Cc1c(cccc1)O

Precursor

IBCZFVVJSBMGBI-UHFFFAOYSA-N

3-Chloro-n-(4-{2-[(2-hydroxyethyl)amino]ethyl}-1,3-thiazol-2-yl)-2-methylbenzenesulfonamide

CC1=C(C=CC=C1Cl)S(=O)(=O)NC2=NC(=CS2)CCNCCO

Environmental

Downstream Successor

QWVGKYWNOKOFNN-UHFFFAOYSA-N

O-Cresol

Cc1c(cccc1)O

Precursor

IBCZFVVJSBMGBI-UHFFFAOYSA-N

3-Chloro-n-(4-{2-[(2-hydroxyethyl)amino]ethyl}-1,3-thiazol-2-yl)-2-methylbenzenesulfonamide

CC1=C(C=CC=C1Cl)S(=O)(=O)NC2=NC(=CS2)CCNCCO

Abiotic

Downstream Successor

IRYAHOGVOVVMOG-UHFFFAOYSA-N

4-Chloro-3-methylcatechol

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

Precursor

IBCZFVVJSBMGBI-UHFFFAOYSA-N

3-Chloro-n-(4-{2-[(2-hydroxyethyl)amino]ethyl}-1,3-thiazol-2-yl)-2-methylbenzenesulfonamide

CC1=C(C=CC=C1Cl)S(=O)(=O)NC2=NC(=CS2)CCNCCO

Environmental

Downstream Successor

LBLYYCQCTBFVLH-UHFFFAOYSA-N

2-Methylbenzenesulfonic acid

S(=O)(=O)(C1=CC=CC=C1C)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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