Description

Methyl 4-(bromomethyl)benzoate (CAS: 2417-72-3) is a high-purity organic compound widely used in pharmaceutical and chemical research. With the molecular formula C₉H₉BrO₂, this versatile reagent serves as a key intermediate in organic synthesis, particularly in the preparation of benzyl derivatives and esterification reactions. Our product is rigorously tested to ensure ≥98% purity, making it ideal for sensitive applications in medicinal chemistry, material science, and cross-coupling reactions. Packaged under inert conditions to preserve stability, this compound is available in quantities ranging from grams to kilograms, with customizable packaging options for laboratory and industrial-scale use.

Key Features:
– High reactivity as a benzyl bromide derivative<br- Compatible with nucleophilic substitution and palladium-catalyzed reactions<br- Suitable for peptide modification and polymer synthesis<br- Strict quality control with batch-specific certificates of analysis

Properties

• CAS Number: 2417-72-3
• Complexity: 151
• IUPAC Name: methyl 4-(bromomethyl)benzoate
• InChI: InChI=1S/C9H9BrO2/c1-12-9(11)8-4-2-7(6-10)3-5-8/h2-5H,6H2,1H3
• InChI Key: NLWBJPPMPLPZIE-UHFFFAOYSA-N
• Exact Mass: 227.97859
• Molecular Formula: C9H9BrO2
• Molecular Weight: 229.07
• SMILES: COC(=O)C1=CC=C(C=C1)CBr
• Topological: 26.3
• Monoisotopic Mass: 227.97859
• Synonyms: Methyl 4-(bromomethyl)benzoate, 2417-72-3, Benzoic acid, 4-(bromomethyl)-, methyl ester, DTXSID4049406, DTXCID3029366, methyl (4-bromomethyl) benzoate, 607-335-7, inchi=1/c9h9bro2/c1-12-9(11)8-4-2-7(6-10)3-5-8/h2-5h,6h2,1h, nlwbjppmplpzie-uhfffaoysa-n, Methyl 4-bromomethylbenzoate, 4-(Bromomethyl)benzoic Acid Methyl Ester, 4-bromomethylbenzoic acid methyl ester, methyl4-(bromomethyl)benzoate, MFCD00032453, methyl-4-(bromomethyl)benzoate, C9GY6V54X6, NSC-83959, methyl p-(bromomethyl)benzoate, p-(Methoxycarbonyl)benzyl bromide, 4-(Methoxycarbonyl)benzyl bromide, 4-carbomethoxybenzyl bromide, 4-Bromomethyl benzoic acid methyl ester, Methyl alpha-Bromo-p-toluate, 4-bromomethyl-benzoic acid methyl ester, methyl-4-bromomethylbenzoate, (4-carbmethoxy)benzylbromide, NCIOpen2_004628, UNII-C9GY6V54X6, SCHEMBL33494, methyl 4-bromomethyl benzoate, methyl-4(bromomethyl)benzoate, (4-carbmethoxy) benzylbromide, p-methoxycarbonylbenzyl bromide, 4-methoxycarbonylbenzyl bromide, 4-(Carbomethoxy)benzyl bromide, Methy 4-(Bromomethyl)Benzoate, methyl (4-bromomethyl)benzoate, methy 4-(bromomethyl) benzoate, methyl 4-(bromomethy) benzoate, Methyl 4-(bromomethy)-benzoate, 4-methoxycarbonyl-benzyl bromide, CHEMBL3183843, methyl 4- (bromomethyl)benzoate, methyl 4-(bromomethyl) benzoate, methyl 4-(bromomethyl)-benzoate, methyl-4-(bromomethyl)-benzoate, Methyl 4-(bromo-methyl)benzoate, 4-methoxy carbonyl benzyl bromide, ALBB-017948, BCP30275, NSC83959, STR03614, Tox21_202815, AB7470, NSC 83959, SBB054899, STK397278, [4-(methoxycarbonyl)-benzyl]-bromide, p-bromomethylbenzoic acid methyl ester, 4bromomethyl-benzoic acid methyl ester, AKOS000119636, Methyl 4-(bromomethyl)benzoate, 98%, AC-4378, alpha-Bromo-p-toluic Acid Methyl Ester, CS-W008845, FM38827, NCGC00260361-01, NCGC00320831-01, 4-(bromo-methyl)benzoic acid methyl ester, 4-(bromomethyl)benzoic acid, methyl ester, CAS-2417-72-3, p-Toluic acid, alpha-bromo-, methyl ester, 4-(bromo-methyl)-benzoic acid methyl ester, DB-046367, B2053, NS00027579, EN300-18210, AB01315911-02, Z57358719, F1019-0028

Methyl 4-(bromomethyl)benzoate is primarily employed as a building block for synthesizing pharmaceutical intermediates and liquid crystal materials. It participates effectively in Suzuki-Miyaura coupling reactions to create biaryl structures. The compound’s reactive bromomethyl group enables facile functionalization of aromatic systems in drug discovery. Researchers utilize it for introducing carboxylate-protected benzyl groups in combinatorial chemistry workflows.

Safety and Hazards

GHS Hazard Statements

• H301 (84%): Toxic if swallowed [Danger Acute toxicity, oral]
• H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]
• H334 (84%): May cause allergy or asthma symptoms or breathing difficulties if inhaled [Danger Sensitization, respiratory]

Precautionary Statements

• P233, P260, P264, P270, P271, P280, P284, P301+P316, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P321, P330, P342+P316, P363, P403, P405, and P501

Hazard Classes and Categories

• Acute Tox. 3 (84%)
• Skin Corr. 1B (100%)
• Resp. Sens. 1 (84%)

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