Description
1,3,5-Tris(bromomethyl)benzene (CAS No. 18226-42-1) is a high-purity brominated aromatic compound with the molecular formula C9H9Br3. This versatile reagent features three reactive bromomethyl groups symmetrically positioned on a benzene ring, making it an ideal building block for organic synthesis, polymer chemistry, and material science applications. With a molecular weight of 344.88 g/mol, this white to off-white crystalline solid exhibits excellent stability under standard conditions. Our product is rigorously tested to ensure ≥98% purity (HPLC) and is packaged under inert atmosphere to guarantee optimal shelf life. Researchers will appreciate its role as a trifunctional linker for dendrimer synthesis, cross-linking agent, or precursor for more complex architectures in pharmaceutical intermediates and advanced materials.
Properties
- CAS Number: 18226-42-1
- Complexity: 91.2
- IUPAC Name: 1,3,5-tris(bromomethyl)benzene
- InChI: InChI=1S/C9H9Br3/c10-4-7-1-8(5-11)3-9(2-7)6-12/h1-3H,4-6H2
- InChI Key: GHITVUOBZBZMND-UHFFFAOYSA-N
- Exact Mass: 355.82339
- Molecular Formula: C9H9Br3
- Molecular Weight: 356.88
- SMILES: C1=C(C=C(C=C1CBr)CBr)CBr
- Monoisotopic Mass: 353.82544
- Synonyms: 1,3,5-Tris(bromomethyl)benzene, 18226-42-1, Benzene, 1,3,5-tris(bromomethyl)-, DTXSID20336232, DTXCID70287321, 629-248-3, ghitvuobzbzmnd-uhfffaoysa-n, 1,3,5-(Tribromomethyl)benzene, MFCD00182500, 1,3,5-Tri(bromomethyl)benzene; 2,4,6-Tri(bromomethyl)benzene; Tribromomesitylene; ?,?’,?”-Tribromomesitylene, alpha,alpha’,alpha”-Tribromomesitylene, tris-(Bromomethyl)benzene, SCHEMBL331501, 1,3,5-trisbromomethyl benzene, WLZ3385, SBB059714, AKOS015836010, CS-W004613, PS-9989, 1,3,5-Tris(bromomethyl)benzene, 97%, AC-25718, PD193106, DB-000106, ST51044619, T2719, EN300-218677, Q27467934
Application
1,3,5-Tris(bromomethyl)benzene serves as a key trifunctional building block in dendrimer synthesis and polymer cross-linking. It finds application in creating star-shaped molecules for advanced material science research and as a precursor for liquid crystalline compounds. The compound’s three reactive sites make it valuable for developing porous organic frameworks and pharmaceutical intermediates requiring symmetrical branching.
Safety and Hazards
GHS Hazard Statements
- H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]
Precautionary Statements
- P260, P264, P280, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P321, P363, P405, and P501
Hazard Classes and Categories
- Skin Corr. 1B (100%)
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