Search More · GCI-TPs

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

Precursor

BBCZXKQLUMQEFC-UHFFFAOYSA-N

N-(2,5-Dichloropentyl)-2,3-dihydro-7-(N-methylsulphamoyl)-1,4-benzodioxin-5-carboxamide

CNS(=O)(=O)C1=CC(=C2C(=C1)OCCO2)C(=O)NCC(CCCCl)Cl

8 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

BBCZXKQLUMQEFC-UHFFFAOYSA-N

N-(2,5-Dichloropentyl)-2,3-dihydro-7-(N-methylsulphamoyl)-1,4-benzodioxin-5-carboxamide

CNS(=O)(=O)C1=CC(=C2C(=C1)OCCO2)C(=O)NCC(CCCCl)Cl

6 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

BBCZXKQLUMQEFC-UHFFFAOYSA-N

N-(2,5-Dichloropentyl)-2,3-dihydro-7-(N-methylsulphamoyl)-1,4-benzodioxin-5-carboxamide

CNS(=O)(=O)C1=CC(=C2C(=C1)OCCO2)C(=O)NCC(CCCCl)Cl

9 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

BBCZXKQLUMQEFC-UHFFFAOYSA-N

N-(2,5-Dichloropentyl)-2,3-dihydro-7-(N-methylsulphamoyl)-1,4-benzodioxin-5-carboxamide

CNS(=O)(=O)C1=CC(=C2C(=C1)OCCO2)C(=O)NCC(CCCCl)Cl

5 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

BBCZXKQLUMQEFC-UHFFFAOYSA-N

N-(2,5-Dichloropentyl)-2,3-dihydro-7-(N-methylsulphamoyl)-1,4-benzodioxin-5-carboxamide

CNS(=O)(=O)C1=CC(=C2C(=C1)OCCO2)C(=O)NCC(CCCCl)Cl

12 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

BBCZXKQLUMQEFC-UHFFFAOYSA-N

N-(2,5-Dichloropentyl)-2,3-dihydro-7-(N-methylsulphamoyl)-1,4-benzodioxin-5-carboxamide

CNS(=O)(=O)C1=CC(=C2C(=C1)OCCO2)C(=O)NCC(CCCCl)Cl

12 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

BBCZXKQLUMQEFC-UHFFFAOYSA-N

N-(2,5-Dichloropentyl)-2,3-dihydro-7-(N-methylsulphamoyl)-1,4-benzodioxin-5-carboxamide

CNS(=O)(=O)C1=CC(=C2C(=C1)OCCO2)C(=O)NCC(CCCCl)Cl

7 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

BBCZXKQLUMQEFC-UHFFFAOYSA-N

N-(2,5-Dichloropentyl)-2,3-dihydro-7-(N-methylsulphamoyl)-1,4-benzodioxin-5-carboxamide

CNS(=O)(=O)C1=CC(=C2C(=C1)OCCO2)C(=O)NCC(CCCCl)Cl

10 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

BBCZXKQLUMQEFC-UHFFFAOYSA-N

N-(2,5-Dichloropentyl)-2,3-dihydro-7-(N-methylsulphamoyl)-1,4-benzodioxin-5-carboxamide

CNS(=O)(=O)C1=CC(=C2C(=C1)OCCO2)C(=O)NCC(CCCCl)Cl

10 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

BBCZXKQLUMQEFC-UHFFFAOYSA-N

N-(2,5-Dichloropentyl)-2,3-dihydro-7-(N-methylsulphamoyl)-1,4-benzodioxin-5-carboxamide

CNS(=O)(=O)C1=CC(=C2C(=C1)OCCO2)C(=O)NCC(CCCCl)Cl

15 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

BBCZXKQLUMQEFC-UHFFFAOYSA-N

N-(2,5-Dichloropentyl)-2,3-dihydro-7-(N-methylsulphamoyl)-1,4-benzodioxin-5-carboxamide

CNS(=O)(=O)C1=CC(=C2C(=C1)OCCO2)C(=O)NCC(CCCCl)Cl

Abiotic

Downstream Successor

BAVYZALUXZFZLV-UHFFFAOYSA-N

Methylamine

Precursor

BBCZXKQLUMQEFC-UHFFFAOYSA-N

N-(2,5-Dichloropentyl)-2,3-dihydro-7-(N-methylsulphamoyl)-1,4-benzodioxin-5-carboxamide

CNS(=O)(=O)C1=CC(=C2C(=C1)OCCO2)C(=O)NCC(CCCCl)Cl

Environmental

Downstream Successor

BAVYZALUXZFZLV-UHFFFAOYSA-N

Methylamine

Precursor

BBCZXKQLUMQEFC-UHFFFAOYSA-N

N-(2,5-Dichloropentyl)-2,3-dihydro-7-(N-methylsulphamoyl)-1,4-benzodioxin-5-carboxamide

CNS(=O)(=O)C1=CC(=C2C(=C1)OCCO2)C(=O)NCC(CCCCl)Cl

Environmental

Downstream Successor

BAVYZALUXZFZLV-UHFFFAOYSA-N

Methylamine

Precursor

BBCZXKQLUMQEFC-UHFFFAOYSA-N

N-(2,5-Dichloropentyl)-2,3-dihydro-7-(N-methylsulphamoyl)-1,4-benzodioxin-5-carboxamide

CNS(=O)(=O)C1=CC(=C2C(=C1)OCCO2)C(=O)NCC(CCCCl)Cl

Abiotic

Downstream Successor

BAVYZALUXZFZLV-UHFFFAOYSA-N

Methylamine

Precursor

BBCZXKQLUMQEFC-UHFFFAOYSA-N

N-(2,5-Dichloropentyl)-2,3-dihydro-7-(N-methylsulphamoyl)-1,4-benzodioxin-5-carboxamide

CNS(=O)(=O)C1=CC(=C2C(=C1)OCCO2)C(=O)NCC(CCCCl)Cl

Abiotic

Downstream Successor

MYMDOKBFMTVEGE-UHFFFAOYSA-N

Methylsulfamic acid

S(=O)(=O)(NC)O

Precursor

BBCZXKQLUMQEFC-UHFFFAOYSA-N

N-(2,5-Dichloropentyl)-2,3-dihydro-7-(N-methylsulphamoyl)-1,4-benzodioxin-5-carboxamide

CNS(=O)(=O)C1=CC(=C2C(=C1)OCCO2)C(=O)NCC(CCCCl)Cl

Environmental

Downstream Successor

CPQCSJYYDADLCZ-UHFFFAOYSA-N

Methylhydroxylamine

N(C)O

Precursor

BBCZXKQLUMQEFC-UHFFFAOYSA-N

N-(2,5-Dichloropentyl)-2,3-dihydro-7-(N-methylsulphamoyl)-1,4-benzodioxin-5-carboxamide

CNS(=O)(=O)C1=CC(=C2C(=C1)OCCO2)C(=O)NCC(CCCCl)Cl

Abiotic

Downstream Successor

CPQCSJYYDADLCZ-UHFFFAOYSA-N

Methylhydroxylamine

N(C)O

Precursor

BBCZXKQLUMQEFC-UHFFFAOYSA-N

N-(2,5-Dichloropentyl)-2,3-dihydro-7-(N-methylsulphamoyl)-1,4-benzodioxin-5-carboxamide

CNS(=O)(=O)C1=CC(=C2C(=C1)OCCO2)C(=O)NCC(CCCCl)Cl

Abiotic

Downstream Successor

KFAUCDBUVPJWSB-UHFFFAOYSA-N

2,5-Dichloropentylamine

NCC(CCCCl)Cl

Precursor

BBCZXKQLUMQEFC-UHFFFAOYSA-N

N-(2,5-Dichloropentyl)-2,3-dihydro-7-(N-methylsulphamoyl)-1,4-benzodioxin-5-carboxamide

CNS(=O)(=O)C1=CC(=C2C(=C1)OCCO2)C(=O)NCC(CCCCl)Cl

Environmental

Downstream Successor

KFAUCDBUVPJWSB-UHFFFAOYSA-N

2,5-Dichloropentylamine

NCC(CCCCl)Cl

Precursor

BBCZXKQLUMQEFC-UHFFFAOYSA-N

N-(2,5-Dichloropentyl)-2,3-dihydro-7-(N-methylsulphamoyl)-1,4-benzodioxin-5-carboxamide

CNS(=O)(=O)C1=CC(=C2C(=C1)OCCO2)C(=O)NCC(CCCCl)Cl

Environmental

Downstream Successor

QTEJVBBGRUHZRR-UHFFFAOYSA-N

2,5-Dichloropentan-1-ol

C(C(CCCCl)Cl)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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