Graphs show a maximum of 100 compounds. Use downloads for complete results.
Depiction
Precursor
XARCTBKSZCJXNO-UHFFFAOYSA-N
2-(2-Methoxyethoxy)ethyl 3-(1,3-benzothiazol-2-yl)-7-(diethylamino)-2-oxochromene-4-carboxylate
CCN(CC)C1=CC2=C(C=C1)C(=C(C(=O)O2)C3=NC4=CC=CC=C4S3)C(=O)OCCOCCOC
5 steps
Depiction
Dead-End Product
BDAGIHXWWSANSR-UHFFFAOYSA-N
Formic Acid
OC=O
Depiction
Precursor
XARCTBKSZCJXNO-UHFFFAOYSA-N
2-(2-Methoxyethoxy)ethyl 3-(1,3-benzothiazol-2-yl)-7-(diethylamino)-2-oxochromene-4-carboxylate
CCN(CC)C1=CC2=C(C=C1)C(=C(C(=O)O2)C3=NC4=CC=CC=C4S3)C(=O)OCCOCCOC
7 steps
Depiction
Dead-End Product
BVKZGUZCCUSVTD-UHFFFAOYSA-N
Carbonic Acid
C(=O)(O)O
Depiction
Precursor
XARCTBKSZCJXNO-UHFFFAOYSA-N
2-(2-Methoxyethoxy)ethyl 3-(1,3-benzothiazol-2-yl)-7-(diethylamino)-2-oxochromene-4-carboxylate
CCN(CC)C1=CC2=C(C=C1)C(=C(C(=O)O2)C3=NC4=CC=CC=C4S3)C(=O)OCCOCCOC
5 steps
Depiction
Dead-End Product
MUBZPKHOEPUJKR-UHFFFAOYSA-N
Oxalic Acid
C(=O)(C(O)=O)O
Depiction
Precursor
XARCTBKSZCJXNO-UHFFFAOYSA-N
2-(2-Methoxyethoxy)ethyl 3-(1,3-benzothiazol-2-yl)-7-(diethylamino)-2-oxochromene-4-carboxylate
CCN(CC)C1=CC2=C(C=C1)C(=C(C(=O)O2)C3=NC4=CC=CC=C4S3)C(=O)OCCOCCOC
9 steps
Depiction
Dead-End Product
CKFGINPQOCXMAZ-UHFFFAOYSA-N
Methanediol
C(O)O
Depiction
Precursor
XARCTBKSZCJXNO-UHFFFAOYSA-N
2-(2-Methoxyethoxy)ethyl 3-(1,3-benzothiazol-2-yl)-7-(diethylamino)-2-oxochromene-4-carboxylate
CCN(CC)C1=CC2=C(C=C1)C(=C(C(=O)O2)C3=NC4=CC=CC=C4S3)C(=O)OCCOCCOC
9 steps
Depiction
Dead-End Product
HEPCJCVNHBXRBO-UHFFFAOYSA-N
Succinyl-carboxylic acid
C(CCC(=O)C(=O)O)(=O)C(O)=O
Depiction
Precursor
XARCTBKSZCJXNO-UHFFFAOYSA-N
2-(2-Methoxyethoxy)ethyl 3-(1,3-benzothiazol-2-yl)-7-(diethylamino)-2-oxochromene-4-carboxylate
CCN(CC)C1=CC2=C(C=C1)C(=C(C(=O)O2)C3=NC4=CC=CC=C4S3)C(=O)OCCOCCOC
10 steps
Depiction
Dead-End Product
LJDZFAPLPVPTBD-UHFFFAOYSA-M
CID 22568690
C([N+](=O)[O-])([O-])=O
Depiction
Precursor
XARCTBKSZCJXNO-UHFFFAOYSA-N
2-(2-Methoxyethoxy)ethyl 3-(1,3-benzothiazol-2-yl)-7-(diethylamino)-2-oxochromene-4-carboxylate
CCN(CC)C1=CC2=C(C=C1)C(=C(C(=O)O2)C3=NC4=CC=CC=C4S3)C(=O)OCCOCCOC
11 steps
Depiction
Dead-End Product
WCJLIWFWHPOTAC-UHFFFAOYSA-N
Rhodizonic acid
c1(c(c(=O)c(c(c1=O)O)O)=O)=O
Depiction
Precursor
XARCTBKSZCJXNO-UHFFFAOYSA-N
2-(2-Methoxyethoxy)ethyl 3-(1,3-benzothiazol-2-yl)-7-(diethylamino)-2-oxochromene-4-carboxylate
CCN(CC)C1=CC2=C(C=C1)C(=C(C(=O)O2)C3=NC4=CC=CC=C4S3)C(=O)OCCOCCOC
10 steps
Depiction
Dead-End Product
ATRULDXOZAITDR-ARJAWSKDSA-N
C(=C=C=C(O)C(=O)O)C(O)=O

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

Depiction
Precursor
XARCTBKSZCJXNO-UHFFFAOYSA-N
2-(2-Methoxyethoxy)ethyl 3-(1,3-benzothiazol-2-yl)-7-(diethylamino)-2-oxochromene-4-carboxylate
CCN(CC)C1=CC2=C(C=C1)C(=C(C(=O)O2)C3=NC4=CC=CC=C4S3)C(=O)OCCOCCOC
Abiotic
Depiction
Downstream Successor
IKHGUXGNUITLKF-UHFFFAOYSA-N
Acetaldehyde
C(C)=O
Depiction
Precursor
XARCTBKSZCJXNO-UHFFFAOYSA-N
2-(2-Methoxyethoxy)ethyl 3-(1,3-benzothiazol-2-yl)-7-(diethylamino)-2-oxochromene-4-carboxylate
CCN(CC)C1=CC2=C(C=C1)C(=C(C(=O)O2)C3=NC4=CC=CC=C4S3)C(=O)OCCOCCOC
PriorBiotransformation
Depiction
Downstream Successor
IKHGUXGNUITLKF-UHFFFAOYSA-N
Acetaldehyde
C(C)=O
Depiction
Precursor
XARCTBKSZCJXNO-UHFFFAOYSA-N
2-(2-Methoxyethoxy)ethyl 3-(1,3-benzothiazol-2-yl)-7-(diethylamino)-2-oxochromene-4-carboxylate
CCN(CC)C1=CC2=C(C=C1)C(=C(C(=O)O2)C3=NC4=CC=CC=C4S3)C(=O)OCCOCCOC
Abiotic
Depiction
Downstream Successor
HPNMFZURTQLUMO-UHFFFAOYSA-O
Diethylammonium
CC[NH2+]CC
Depiction
Precursor
XARCTBKSZCJXNO-UHFFFAOYSA-N
2-(2-Methoxyethoxy)ethyl 3-(1,3-benzothiazol-2-yl)-7-(diethylamino)-2-oxochromene-4-carboxylate
CCN(CC)C1=CC2=C(C=C1)C(=C(C(=O)O2)C3=NC4=CC=CC=C4S3)C(=O)OCCOCCOC
Abiotic
Depiction
Downstream Successor
HPNMFZURTQLUMO-UHFFFAOYSA-O
Diethylammonium
CC[NH2+]CC
Depiction
Precursor
XARCTBKSZCJXNO-UHFFFAOYSA-N
2-(2-Methoxyethoxy)ethyl 3-(1,3-benzothiazol-2-yl)-7-(diethylamino)-2-oxochromene-4-carboxylate
CCN(CC)C1=CC2=C(C=C1)C(=C(C(=O)O2)C3=NC4=CC=CC=C4S3)C(=O)OCCOCCOC
Abiotic
Depiction
Downstream Successor
QUSNBJAOOMFDIB-UHFFFAOYSA-N
Ethylamine
NCC
Depiction
Precursor
XARCTBKSZCJXNO-UHFFFAOYSA-N
2-(2-Methoxyethoxy)ethyl 3-(1,3-benzothiazol-2-yl)-7-(diethylamino)-2-oxochromene-4-carboxylate
CCN(CC)C1=CC2=C(C=C1)C(=C(C(=O)O2)C3=NC4=CC=CC=C4S3)C(=O)OCCOCCOC
Abiotic
Depiction
Downstream Successor
TYDFLVGVWMSQAC-UHFFFAOYSA-O
CC[NH+](CC)Cl
Depiction
Precursor
XARCTBKSZCJXNO-UHFFFAOYSA-N
2-(2-Methoxyethoxy)ethyl 3-(1,3-benzothiazol-2-yl)-7-(diethylamino)-2-oxochromene-4-carboxylate
CCN(CC)C1=CC2=C(C=C1)C(=C(C(=O)O2)C3=NC4=CC=CC=C4S3)C(=O)OCCOCCOC
Abiotic
Depiction
Downstream Successor
FVCOIAYSJZGECG-UHFFFAOYSA-N
Diethylhydroxylamine
CCN(CC)O
Depiction
Precursor
XARCTBKSZCJXNO-UHFFFAOYSA-N
2-(2-Methoxyethoxy)ethyl 3-(1,3-benzothiazol-2-yl)-7-(diethylamino)-2-oxochromene-4-carboxylate
CCN(CC)C1=CC2=C(C=C1)C(=C(C(=O)O2)C3=NC4=CC=CC=C4S3)C(=O)OCCOCCOC
Abiotic
Depiction
Downstream Successor
FVCOIAYSJZGECG-UHFFFAOYSA-N
Diethylhydroxylamine
CCN(CC)O
Depiction
Precursor
XARCTBKSZCJXNO-UHFFFAOYSA-N
2-(2-Methoxyethoxy)ethyl 3-(1,3-benzothiazol-2-yl)-7-(diethylamino)-2-oxochromene-4-carboxylate
CCN(CC)C1=CC2=C(C=C1)C(=C(C(=O)O2)C3=NC4=CC=CC=C4S3)C(=O)OCCOCCOC
Abiotic
Depiction
Downstream Successor
MIJDSYMOBYNHOT-UHFFFAOYSA-N
2-(Ethylamino)ethanol
OCCNCC
Depiction
Precursor
XARCTBKSZCJXNO-UHFFFAOYSA-N
2-(2-Methoxyethoxy)ethyl 3-(1,3-benzothiazol-2-yl)-7-(diethylamino)-2-oxochromene-4-carboxylate
CCN(CC)C1=CC2=C(C=C1)C(=C(C(=O)O2)C3=NC4=CC=CC=C4S3)C(=O)OCCOCCOC
Abiotic
Depiction
Downstream Successor
RLNVKYOMCJCALP-UHFFFAOYSA-N
CCN(CC)C(=CC(O)=O)C=CC(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.

Search with another depth
or Explore another compound
Higher depth reveals distant relationships but increases loading time.