Description

3-Amino-4-chlorobenzamide (CAS No. 19694-10-1) is a high-purity benzamide derivative with the molecular formula C₇H₇ClN₂O. This fine chemical is characterized by its amino and chloro functional groups at the 3- and 4-positions of the benzamide ring, making it a valuable intermediate in organic synthesis and pharmaceutical research. Suitable for laboratory and industrial use, our product is rigorously tested to ensure ≥98% purity (HPLC) and is supplied as a crystalline solid with excellent batch-to-batch consistency. Ideal for researchers developing novel heterocyclic compounds, PARP inhibitors, or agrochemicals. Available in scalable quantities from milligrams to kilograms with customizable packaging under inert atmosphere for stability.

Properties

• CAS Number: 19694-10-1
• Complexity: 163
• IUPAC Name: 3-amino-4-chloro-benzamide
• InChI: InChI=1S/C7H7ClN2O/c8-5-2-1-4(7(10)11)3-6(5)9/h1-3H,9H2,(H2,10,11)
• InChI Key: QHMDKGRWJVOUFU-UHFFFAOYSA-N
• Exact Mass: 170.0246905
• Molecular Formula: C7H7ClN2O
• Molecular Weight: 170.59
• SMILES: C1=CC(=C(C=C1C(=O)N)N)Cl
• Topological: 69.1
• Monoisotopic Mass: 170.0246905
• Synonyms: 3-Amino-4-chlorobenzamide, 19694-10-1, Benzamide, 3-amino-4-chloro-, EINECS 243-231-4, DTXSID2066517, EC 243-231-4, DTXCID4036140, 243-231-4, 19694-86-1, 3-Amino-4-chloro-benzamide, MFCD00035785, 3-Amino-4-chlor-benzoesaeure-amid, EN300-30609, Fast Red Base DB-30, SCHEMBL1808713, SCHEMBL1808714, SCHEMBL7913711, 3-Amino-4-chlorobenzamide, 96%, 3-Amino-4-chlorobenzoic acidamide, BDBM626135, BBL027919, SBB003852, STK899008, AKOS000128877, FA71371, AC-16266, ST077227, SY020313, TS-02318, DB-044945, CS-0127989, NS00005261

Application

3-Amino-4-chlorobenzamide serves as a key building block in medicinal chemistry, particularly in the synthesis of PARP (poly ADP-ribose polymerase) inhibitors for oncology research. Its reactive amino group enables facile derivatization for creating libraries of benzamide-based drug candidates. The compound also finds use in material science as a precursor for functionalized polymers and in agrochemical research for developing novel plant protection agents. Researchers value its dual functionality for selective electrophilic aromatic substitutions.

Safety and Hazards

GHS Hazard Statements

• H315 (93.5%): Causes skin irritation [Warning Skin corrosion/irritation]
• H319 (93.5%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
• H335 (93.5%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]

Precautionary Statements

• P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501

Hazard Classes and Categories

• Skin Irrit. 2 (93.5%)
• Eye Irrit. 2 (93.5%)
• STOT SE 3 (93.5%)

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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.