Description

2-Amino-6-chlorobenzoic acid (CAS No. 2148-56-3) is a high-purity organic compound with the molecular formula C₇H₆ClNO₂. This fine chemical features a benzoic acid backbone substituted with an amino group at the 2-position and a chloro group at the 6-position, making it a valuable intermediate in pharmaceutical and agrochemical synthesis. Our product is rigorously tested to ensure ≥98% purity by HPLC, with controlled levels of heavy metals and residual solvents to meet stringent research standards. Available in crystalline powder form, it is packaged under inert conditions to guarantee stability and longevity. Ideal for use in combinatorial chemistry, medicinal chemistry, and as a building block for heterocyclic compounds.

Properties

• CAS Number: 2148-56-3
• Complexity: 163
• IUPAC Name: 2-amino-6-chloro-benzoic acid
• InChI: InChI=1S/C7H6ClNO2/c8-4-2-1-3-5(9)6(4)7(10)11/h1-3H,9H2,(H,10,11)
• InChI Key: SZCPTRGBOVXVCA-UHFFFAOYSA-N
• Exact Mass: 171.0087061
• Molecular Formula: C7H6ClNO2
• Molecular Weight: 171.58
• SMILES: C1=CC(=C(C(=C1)Cl)C(=O)O)N
• Topological: 63.3
• Monoisotopic Mass: 171.0087061
• Synonyms: 2-Amino-6-chlorobenzoic acid, 2148-56-3, Benzoic acid, 2-amino-6-chloro-, DTXSID40175761, EINECS 218-416-8, NSC 17189, 6CABA cpd, DTXCID1098252, 218-416-8, inchi=1/c7h6clno2/c8-4-2-1-3-5(9)6(4)7(10)11/h1-3h,9h2,(h,10,11, szcptrgbovxvca-uhfffaoysa-n, 6-Chloroanthranilic acid, MFCD00051530, 2-amino-6-chloro-benzoic acid, NSC17189, 6-Chloranthranilsaure, 6-chloro anthranilic acid, 2Amino-6-chlorobenzoic acid, SCHEMBL147437, 2-amino-6-chloro benzoic acid, SCHEMBL1803965, CS-D1462, HY-Y1132, NSC-17189, SBB001735, STK676405, 2-Amino-6-chlorobenzoic acid, 98%, AKOS001741281, AC-1745, FA38608, PS-4143, PD210652, SY001857, DB-005963, ST4054533, C2048, NS00026877, EN300-65916, Z995132230

Application

2-Amino-6-chlorobenzoic acid serves as a key precursor in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs) and other pharmacologically active molecules. Researchers utilize this compound in the development of novel benzodiazepine derivatives and as a scaffold for antimicrobial agents. Its reactive amino and carboxyl groups enable facile derivatization for structure-activity relationship studies in drug discovery programs.

Safety and Hazards

GHS Hazard Statements

• H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
• H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
• H335 (98.1%): 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 (100%)
• Eye Irrit. 2 (100%)
• STOT SE 3 (98.1%)

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