Search More · GCI-TPs

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

Precursor

YFYDYMYITUSDEE-WQRHYEAKSA-N

S-2-benzothiazolyl (Z)-2-(2-aminothiazol-4-yl)-2-acetyloxyiminothioacetate

CC(=O)O/N=C(/C1=CSC(=N1)N)\C(=O)SC2=NC3=CC=CC=C3S2

8 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

YFYDYMYITUSDEE-WQRHYEAKSA-N

S-2-benzothiazolyl (Z)-2-(2-aminothiazol-4-yl)-2-acetyloxyiminothioacetate

CC(=O)O/N=C(/C1=CSC(=N1)N)\C(=O)SC2=NC3=CC=CC=C3S2

5 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

YFYDYMYITUSDEE-WQRHYEAKSA-N

S-2-benzothiazolyl (Z)-2-(2-aminothiazol-4-yl)-2-acetyloxyiminothioacetate

CC(=O)O/N=C(/C1=CSC(=N1)N)\C(=O)SC2=NC3=CC=CC=C3S2

4 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

YFYDYMYITUSDEE-WQRHYEAKSA-N

S-2-benzothiazolyl (Z)-2-(2-aminothiazol-4-yl)-2-acetyloxyiminothioacetate

CC(=O)O/N=C(/C1=CSC(=N1)N)\C(=O)SC2=NC3=CC=CC=C3S2

8 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

YFYDYMYITUSDEE-WQRHYEAKSA-N

S-2-benzothiazolyl (Z)-2-(2-aminothiazol-4-yl)-2-acetyloxyiminothioacetate

CC(=O)O/N=C(/C1=CSC(=N1)N)\C(=O)SC2=NC3=CC=CC=C3S2

8 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

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

Upstream Precursor

YFYDYMYITUSDEE-WQRHYEAKSA-N

S-2-benzothiazolyl (Z)-2-(2-aminothiazol-4-yl)-2-acetyloxyiminothioacetate

CC(=O)O/N=C(/C1=CSC(=N1)N)\C(=O)SC2=NC3=CC=CC=C3S2

Abiotic

Product

YFYDYMYITUSDEE-WQRHYEAKSA-N

S-2-benzothiazolyl (Z)-2-(2-aminothiazol-4-yl)-2-acetyloxyiminothioacetate

CC(=O)O/N=C(/C1=CSC(=N1)N)\C(=O)SC2=NC3=CC=CC=C3S2

Upstream Precursor

YFYDYMYITUSDEE-WQRHYEAKSA-N

S-2-benzothiazolyl (Z)-2-(2-aminothiazol-4-yl)-2-acetyloxyiminothioacetate

CC(=O)O/N=C(/C1=CSC(=N1)N)\C(=O)SC2=NC3=CC=CC=C3S2

Abiotic

Product

YFYDYMYITUSDEE-WQRHYEAKSA-N

S-2-benzothiazolyl (Z)-2-(2-aminothiazol-4-yl)-2-acetyloxyiminothioacetate

CC(=O)O/N=C(/C1=CSC(=N1)N)\C(=O)SC2=NC3=CC=CC=C3S2

Upstream Precursor

YFYDYMYITUSDEE-WQRHYEAKSA-N

S-2-benzothiazolyl (Z)-2-(2-aminothiazol-4-yl)-2-acetyloxyiminothioacetate

CC(=O)O/N=C(/C1=CSC(=N1)N)\C(=O)SC2=NC3=CC=CC=C3S2

Environmental

Product

YFYDYMYITUSDEE-WQRHYEAKSA-N

S-2-benzothiazolyl (Z)-2-(2-aminothiazol-4-yl)-2-acetyloxyiminothioacetate

CC(=O)O/N=C(/C1=CSC(=N1)N)\C(=O)SC2=NC3=CC=CC=C3S2

Upstream Precursor

SCSXPNOPPUBFNF-UHFFFAOYSA-N

C(C(=O)ON=C(C1=CSC(=N1)N)C(=O)SC2=NC3=CC=CC=C3S2)Cl

Abiotic

Product

YFYDYMYITUSDEE-WQRHYEAKSA-N

S-2-benzothiazolyl (Z)-2-(2-aminothiazol-4-yl)-2-acetyloxyiminothioacetate

CC(=O)O/N=C(/C1=CSC(=N1)N)\C(=O)SC2=NC3=CC=CC=C3S2

Upstream Precursor

SCSXPNOPPUBFNF-UHFFFAOYSA-N

C(C(=O)ON=C(C1=CSC(=N1)N)C(=O)SC2=NC3=CC=CC=C3S2)Cl

Environmental

Product

YFYDYMYITUSDEE-WQRHYEAKSA-N

S-2-benzothiazolyl (Z)-2-(2-aminothiazol-4-yl)-2-acetyloxyiminothioacetate

CC(=O)O/N=C(/C1=CSC(=N1)N)\C(=O)SC2=NC3=CC=CC=C3S2

Upstream Precursor

SCSXPNOPPUBFNF-UHFFFAOYSA-N

C(C(=O)ON=C(C1=CSC(=N1)N)C(=O)SC2=NC3=CC=CC=C3S2)Cl

Abiotic

Product

YFYDYMYITUSDEE-WQRHYEAKSA-N

S-2-benzothiazolyl (Z)-2-(2-aminothiazol-4-yl)-2-acetyloxyiminothioacetate

CC(=O)O/N=C(/C1=CSC(=N1)N)\C(=O)SC2=NC3=CC=CC=C3S2

Upstream Precursor

SCSXPNOPPUBFNF-UHFFFAOYSA-N

C(C(=O)ON=C(C1=CSC(=N1)N)C(=O)SC2=NC3=CC=CC=C3S2)Cl

Environmental

Product

YFYDYMYITUSDEE-WQRHYEAKSA-N

S-2-benzothiazolyl (Z)-2-(2-aminothiazol-4-yl)-2-acetyloxyiminothioacetate

CC(=O)O/N=C(/C1=CSC(=N1)N)\C(=O)SC2=NC3=CC=CC=C3S2

Upstream Precursor

IMTPFHSYBJZXJL-UHFFFAOYSA-N

CC(=O)ON=C(C1=CSC(=N1)N)C(=O)S(C2=NC3=CC=CC=C3S2)=O

Abiotic

Product

YFYDYMYITUSDEE-WQRHYEAKSA-N

S-2-benzothiazolyl (Z)-2-(2-aminothiazol-4-yl)-2-acetyloxyiminothioacetate

CC(=O)O/N=C(/C1=CSC(=N1)N)\C(=O)SC2=NC3=CC=CC=C3S2

Upstream Precursor

IMTPFHSYBJZXJL-UHFFFAOYSA-N

CC(=O)ON=C(C1=CSC(=N1)N)C(=O)S(C2=NC3=CC=CC=C3S2)=O

Environmental

Product

YFYDYMYITUSDEE-WQRHYEAKSA-N

S-2-benzothiazolyl (Z)-2-(2-aminothiazol-4-yl)-2-acetyloxyiminothioacetate

CC(=O)O/N=C(/C1=CSC(=N1)N)\C(=O)SC2=NC3=CC=CC=C3S2

Upstream Precursor

SAJSKLFZPHOTPE-UHFFFAOYSA-N

C(C(=O)ON=C(C1=CSC(=N1)N)C(=O)S(C2=NC3=CC=CC=C3S2)=O)Cl

Abiotic

Product

YFYDYMYITUSDEE-WQRHYEAKSA-N

S-2-benzothiazolyl (Z)-2-(2-aminothiazol-4-yl)-2-acetyloxyiminothioacetate

CC(=O)O/N=C(/C1=CSC(=N1)N)\C(=O)SC2=NC3=CC=CC=C3S2

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

Precursor

YFYDYMYITUSDEE-WQRHYEAKSA-N

S-2-benzothiazolyl (Z)-2-(2-aminothiazol-4-yl)-2-acetyloxyiminothioacetate

CC(=O)O/N=C(/C1=CSC(=N1)N)\C(=O)SC2=NC3=CC=CC=C3S2

Environmental

Downstream Successor

QTBSBXVTEAMEQO-UHFFFAOYSA-N

Acetic Acid

CC(=O)O

Precursor

YFYDYMYITUSDEE-WQRHYEAKSA-N

S-2-benzothiazolyl (Z)-2-(2-aminothiazol-4-yl)-2-acetyloxyiminothioacetate

CC(=O)O/N=C(/C1=CSC(=N1)N)\C(=O)SC2=NC3=CC=CC=C3S2

Environmental

Downstream Successor

FOCAUTSVDIKZOP-UHFFFAOYSA-M

Chloroacetate

[O-]C(=O)CCl

Precursor

YFYDYMYITUSDEE-WQRHYEAKSA-N

S-2-benzothiazolyl (Z)-2-(2-aminothiazol-4-yl)-2-acetyloxyiminothioacetate

CC(=O)O/N=C(/C1=CSC(=N1)N)\C(=O)SC2=NC3=CC=CC=C3S2

Abiotic

Downstream Successor

FOCAUTSVDIKZOP-UHFFFAOYSA-M

Chloroacetate

[O-]C(=O)CCl

Precursor

YFYDYMYITUSDEE-WQRHYEAKSA-N

S-2-benzothiazolyl (Z)-2-(2-aminothiazol-4-yl)-2-acetyloxyiminothioacetate

CC(=O)O/N=C(/C1=CSC(=N1)N)\C(=O)SC2=NC3=CC=CC=C3S2

Environmental

Downstream Successor

AEMRFAOFKBGASW-UHFFFAOYSA-N

Glycolic Acid

C(=O)(CO)O

Precursor

YFYDYMYITUSDEE-WQRHYEAKSA-N

S-2-benzothiazolyl (Z)-2-(2-aminothiazol-4-yl)-2-acetyloxyiminothioacetate

CC(=O)O/N=C(/C1=CSC(=N1)N)\C(=O)SC2=NC3=CC=CC=C3S2

Environmental

Downstream Successor

YXIWHUQXZSMYRE-UHFFFAOYSA-N

2-Mercaptobenzothiazole

SC1=NC2=CC=CC=C2S1

Precursor

YFYDYMYITUSDEE-WQRHYEAKSA-N

S-2-benzothiazolyl (Z)-2-(2-aminothiazol-4-yl)-2-acetyloxyiminothioacetate

CC(=O)O/N=C(/C1=CSC(=N1)N)\C(=O)SC2=NC3=CC=CC=C3S2

Environmental

Downstream Successor

MBFGXOJFSSAHQF-UHFFFAOYSA-N

1-oxo-3H-1,3-benzothiazole-2-thione

C1=CC=C2C(=C1)N=C(S2=O)S

Precursor

YFYDYMYITUSDEE-WQRHYEAKSA-N

S-2-benzothiazolyl (Z)-2-(2-aminothiazol-4-yl)-2-acetyloxyiminothioacetate

CC(=O)O/N=C(/C1=CSC(=N1)N)\C(=O)SC2=NC3=CC=CC=C3S2

Environmental

Downstream Successor

NLBKRTONWJNTOH-UHFFFAOYSA-N

OC1=CC2=C(C=C1O)NC(=S)S2

Precursor

YFYDYMYITUSDEE-WQRHYEAKSA-N

S-2-benzothiazolyl (Z)-2-(2-aminothiazol-4-yl)-2-acetyloxyiminothioacetate

CC(=O)O/N=C(/C1=CSC(=N1)N)\C(=O)SC2=NC3=CC=CC=C3S2

Environmental

Downstream Successor

MAUQVWNRJMKSFW-UHFFFAOYSA-N

6,7-Dihydroxy-2-mercaptobenzothiazole

OC1=C(C2=C(C=C1)NC(=S)S2)O

Precursor

YFYDYMYITUSDEE-WQRHYEAKSA-N

S-2-benzothiazolyl (Z)-2-(2-aminothiazol-4-yl)-2-acetyloxyiminothioacetate

CC(=O)O/N=C(/C1=CSC(=N1)N)\C(=O)SC2=NC3=CC=CC=C3S2

Environmental

Downstream Successor

OBRMMFBYPFFKFA-UHFFFAOYSA-N

2-(2-Aminothiazole-4-yl)-2-acetoxyiminoacetic acid

CC(=O)ON=C(C1=CSC(=N1)N)C(=O)O

Precursor

YFYDYMYITUSDEE-WQRHYEAKSA-N

S-2-benzothiazolyl (Z)-2-(2-aminothiazol-4-yl)-2-acetyloxyiminothioacetate

CC(=O)O/N=C(/C1=CSC(=N1)N)\C(=O)SC2=NC3=CC=CC=C3S2

Environmental

Downstream Successor

OBRMMFBYPFFKFA-UHFFFAOYSA-N

2-(2-Aminothiazole-4-yl)-2-acetoxyiminoacetic acid

CC(=O)ON=C(C1=CSC(=N1)N)C(=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.

Search with another depth

Depth:

or Explore another compound

Higher depth reveals distant relationships but increases loading time.