This compound is a chlorinated aromatic amide used as a pharmaceutical intermediate in the synthesis of benzodiazepines. Its structure features an amide linkage, aromatic rings, and halogen substituents, contributing to its role in organic synthesis.
Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.
Sourcing 2-Chloro-N-(2-(2-chlorobenzoyl)-4-nitrophenyl)acetamide?
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2,2'-Iminobis[N-[2-(2-chlorobenzoyl)-4-nitrophenyl]acetamide]
pharmaceutical intermediate
2-Bromo-N-(2-(2-chlorobenzoyl)-4-nitrophenyl)acetamide
pharmaceutical intermediate
2-Amino-N-(2-(2-chlorobenzoyl)-4-nitrophenyl)acetamide monohydrochloride
pharmaceutical intermediate
Clonazafone desglycyl
pharmaceutical intermediate
N-(2-Benzoyl-4-chlorophenyl)acetamide
pharmaceutical intermediate
2-amino-2',5-dichlorobenzophenone
pharmaceutical intermediate
7-Chloro-2-methoxy-5-phenyl-3H-1,4-benzodiazepine
pharmaceutical intermediate
Methanone, (2-amino-5-chlorophenyl)(4-hydroxyphenyl)-
pharmaceutical intermediate
The international HS code for 2-Chloro-N-(2-(2-chlorobenzoyl)-4-nitrophenyl)acetamide (CAS 180854-85-7) is 2924.29.
2924.29
2924 29 70
Classification per the EU customs inventory ECICS (2026-07 snapshot, HS 2022). National tariff lines and product form can affect the final classification.
2-chloro-N-[2-(2-chlorobenzoyl)-4-nitrophenyl]acetamide
YBAJRIMWOFPRTG-UHFFFAOYSA-N
C1=CC=C(C(=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])NC(=O)CCl)Cl
Sourcing 2-Chloro-N-(2-(2-chlorobenzoyl)-4-nitrophenyl)acetamide?
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