Description

4-Amino-N-methylbenzamide (CAS No. 6274-22-2) is a high-purity organic compound with the molecular formula C₈H₁₀N₂O. This fine chemical is widely utilized in pharmaceutical research, agrochemical development, and material science due to its versatile amide and aromatic amine functional groups. Our product is rigorously tested to ensure ≥98% purity (HPLC), making it ideal for synthetic applications, reference standards, and biochemical studies. Supplied as a white to off-white crystalline powder, it is packaged under inert conditions to guarantee stability and shelf life. Suitable for laboratory and industrial-scale use, this compound is available in quantities ranging from milligrams to kilograms, with custom synthesis options available upon request.

Properties

• CAS Number: 6274-22-2
• Complexity: 139
• IUPAC Name: 4-amino-N-methyl-benzamide
• InChI: InChI=1S/C8H10N2O/c1-10-8(11)6-2-4-7(9)5-3-6/h2-5H,9H2,1H3,(H,10,11)
• InChI Key: XAGFYNSCWICYPA-UHFFFAOYSA-N
• Exact Mass: 150.079312947
• Molecular Formula: C8H10N2O
• Molecular Weight: 150.18
• SMILES: CNC(=O)C1=CC=C(C=C1)N
• Topological: 55.1
• Monoisotopic Mass: 150.079312947
• Synonyms: 4-amino-N-methylbenzamide, DTXSID70284370, DTXCID90235521, 677-113-2, 6274-22-2, 4-(methylcarbamyl)aniline, N-Methyl 4-aminobenzamide, 4-Amino-N-methyl-benzamide, MFCD00665792, CHEMBL165728, (4-aminophenyl)-N-methylcarboxamide, Benzamide, 4-amino-N-methyl-, 4-(Methylcarbamoyl)aniline, NSC36985, N-methyl-p-aminobenzamide, TimTec1_002294, SCHEMBL158878, 4-?Amino-?N-?methylbenzamide, SCHEMBL2643011, SCHEMBL16336479, SCHEMBL28139334, HMS1540I06, ALBB-002184, Benzamide,4-amino-N-methyl-(9ci), BBL012115, BDBM50623066, NSC-36985, SBB000104, STK414012, AKOS000264278, 4-Amino-N-methylbenzamide, AldrichCPR, AC-7292, CS-W018773, PS-4540, SB76619, ST029313, SY005511, DB-028699, A2064, EN300-09745, Z56985799, F5608-0068

4-Amino-N-methylbenzamide serves as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and anticancer agents. Its amide and amino groups enable facile derivatization for structure-activity relationship (SAR) studies. Researchers also employ it in peptide-mimetic designs and as a building block for advanced materials. In agrochemical research, it contributes to the development of novel herbicides and fungicides.

Safety and Hazards

GHS Hazard Statements

• H302 (97.5%): Harmful if swallowed [Warning Acute toxicity, oral]

Precautionary Statements

• P264, P270, P301+P317, P330, and P501

Hazard Classes and Categories

• Acute Tox. 4 (97.5%)

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