Search More · GCI-TPs

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

Precursor

ZHJLHAOWFYEIOC-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)-2-chloroacetamide

C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl

6 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

ZHJLHAOWFYEIOC-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)-2-chloroacetamide

C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl

3 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

ZHJLHAOWFYEIOC-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)-2-chloroacetamide

C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl

3 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

ZHJLHAOWFYEIOC-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)-2-chloroacetamide

C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl

4 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

ZHJLHAOWFYEIOC-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)-2-chloroacetamide

C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl

6 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

ZHJLHAOWFYEIOC-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)-2-chloroacetamide

C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl

6 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

ZHJLHAOWFYEIOC-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)-2-chloroacetamide

C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl

6 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

ZHJLHAOWFYEIOC-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)-2-chloroacetamide

C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl

13 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

ZHJLHAOWFYEIOC-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)-2-chloroacetamide

C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl

13 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

ZHJLHAOWFYEIOC-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)-2-chloroacetamide

C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl

7 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.

Upstream Precursor

USZJZGVAIGKLRF-UHFFFAOYSA-N

N-(2-benzoyl-4-nitrophenyl)-2-bromoacetamide

C1=CC=CC(=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CBr

Abiotic

Product

ZHJLHAOWFYEIOC-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)-2-chloroacetamide

C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl

Upstream Precursor

USZJZGVAIGKLRF-UHFFFAOYSA-N

N-(2-benzoyl-4-nitrophenyl)-2-bromoacetamide

C1=CC=CC(=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CBr

Environmental

Product

ZHJLHAOWFYEIOC-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)-2-chloroacetamide

C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl

Upstream Precursor

DGIHQJAKOHGCOQ-UHFFFAOYSA-N

2-Bromo-N-[2-(2-fluorobenzoyl)-4-nitrophenyl]acetamide

N(C1=C(C=C(C=C1)[N+](=O)[O-])C(=O)C2=CC=CC=C2F)C(=O)CBr

Abiotic

Product

ZHJLHAOWFYEIOC-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)-2-chloroacetamide

C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl

Upstream Precursor

DGIHQJAKOHGCOQ-UHFFFAOYSA-N

2-Bromo-N-[2-(2-fluorobenzoyl)-4-nitrophenyl]acetamide

N(C1=C(C=C(C=C1)[N+](=O)[O-])C(=O)C2=CC=CC=C2F)C(=O)CBr

Environmental

Product

ZHJLHAOWFYEIOC-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)-2-chloroacetamide

C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl

Upstream Precursor

ZHJLHAOWFYEIOC-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)-2-chloroacetamide

C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl

Abiotic

Product

ZHJLHAOWFYEIOC-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)-2-chloroacetamide

C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl

Upstream Precursor

ZHJLHAOWFYEIOC-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)-2-chloroacetamide

C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl

Environmental

Product

ZHJLHAOWFYEIOC-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)-2-chloroacetamide

C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl

Upstream Precursor

XSTMFEOLMKEEMU-UHFFFAOYSA-N

2-bromo-N-[2-(2-chlorobenzoyl)-4-nitrophenyl]acetamide

C1=CC=C(C(=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CBr)Cl

Abiotic

Product

ZHJLHAOWFYEIOC-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)-2-chloroacetamide

C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl

Upstream Precursor

XSTMFEOLMKEEMU-UHFFFAOYSA-N

2-bromo-N-[2-(2-chlorobenzoyl)-4-nitrophenyl]acetamide

C1=CC=C(C(=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CBr)Cl

Environmental

Product

ZHJLHAOWFYEIOC-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)-2-chloroacetamide

C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl

Upstream Precursor

PGXLULGZZOZXRW-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)acetamide

C1=CC=CC(=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)C

Abiotic

Product

ZHJLHAOWFYEIOC-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)-2-chloroacetamide

C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl

Upstream Precursor

PGXLULGZZOZXRW-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)acetamide

C1=CC=CC(=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)C

Abiotic

Product

ZHJLHAOWFYEIOC-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)-2-chloroacetamide

C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl

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

Precursor

ZHJLHAOWFYEIOC-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)-2-chloroacetamide

C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl

Abiotic

Downstream Successor

FOCAUTSVDIKZOP-UHFFFAOYSA-M

Chloroacetate

[O-]C(=O)CCl

Precursor

ZHJLHAOWFYEIOC-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)-2-chloroacetamide

C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl

Environmental

Downstream Successor

FOCAUTSVDIKZOP-UHFFFAOYSA-M

Chloroacetate

[O-]C(=O)CCl

Precursor

ZHJLHAOWFYEIOC-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)-2-chloroacetamide

C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl

Abiotic

Downstream Successor

FOCAUTSVDIKZOP-UHFFFAOYSA-M

Chloroacetate

[O-]C(=O)CCl

Precursor

ZHJLHAOWFYEIOC-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)-2-chloroacetamide

C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl

Environmental

Downstream Successor

FOCAUTSVDIKZOP-UHFFFAOYSA-M

Chloroacetate

[O-]C(=O)CCl

Precursor

ZHJLHAOWFYEIOC-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)-2-chloroacetamide

C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl

Environmental

Downstream Successor

AEMRFAOFKBGASW-UHFFFAOYSA-N

Glycolic Acid

C(=O)(CO)O

Precursor

ZHJLHAOWFYEIOC-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)-2-chloroacetamide

C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl

Abiotic

Downstream Successor

AEMRFAOFKBGASW-UHFFFAOYSA-N

Glycolic Acid

C(=O)(CO)O

Precursor

ZHJLHAOWFYEIOC-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)-2-chloroacetamide

C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl

Environmental

Downstream Successor

DLFVBJFMPXGRIB-UHFFFAOYSA-N

Acetamide

NC(=O)C

Precursor

ZHJLHAOWFYEIOC-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)-2-chloroacetamide

C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl

Abiotic

Downstream Successor

DLFVBJFMPXGRIB-UHFFFAOYSA-N

Acetamide

NC(=O)C

Precursor

ZHJLHAOWFYEIOC-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)-2-chloroacetamide

C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl

Environmental

Downstream Successor

VXIVSQZSERGHQP-UHFFFAOYSA-N

Chloroacetamide

C(C(N)=O)Cl

Precursor

ZHJLHAOWFYEIOC-UHFFFAOYSA-N

N-(2-Benzoyl-4-nitrophenyl)-2-chloroacetamide

C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl

Environmental

Downstream Successor

FAQJJMHZNSSFSM-UHFFFAOYSA-N

Phenylglyoxylic Acid

c1cccc(c1)C(C(O)=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.

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