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4-(bromomethyl)benzaldehyde

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4-(bromomethyl)benzaldehyde Basic information
Product Name:4-(bromomethyl)benzaldehyde
Synonyms:4-(BROMOMETHYL)BENZALDEHYDE;4-(Bromomethyl)benzaldehyde 97%;Benzaldehyde,4-(broMoMethyl)-;4-(Bromomethyl)benzaldehyde97%;α-Bromo-p-Tolualdehyde;4-Formylbenzyl bromide, alpha-Bromo-4-formyltoluene
CAS:51359-78-5
MF:C8H7BrO
MW:199.04
EINECS:
Product Categories:pharmacetical;Methyl Halides;Phenyls & Phenyl-Het;Methyl Halides;Phenyls & Phenyl-Het
Mol File:51359-78-5.mol
4-(bromomethyl)benzaldehyde Structure
4-(bromomethyl)benzaldehyde Chemical Properties
Melting point 99 °C
Boiling point 277.9±15.0 °C(Predicted)
density 1.524±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
form crystalline powder
color Pale lemon
InChIInChI=1S/C8H7BrO/c9-5-7-1-3-8(6-10)4-2-7/h1-4,6H,5H2
InChIKeyXYPVBKDHERGKJG-UHFFFAOYSA-N
SMILESC(=O)C1=CC=C(CBr)C=C1
CAS DataBase Reference51359-78-5
Safety Information
Hazard Codes C
Safety Statements 24/25
Hazard Note Corrosive
HS Code 29142990
MSDS Information
4-(bromomethyl)benzaldehyde Usage And Synthesis
Synthesis 4-(bromomethyl) benzonitrile (1 g, 5.1 mmol) was dissolved in 10 mL of dry toluene and cooled at 0 oC and a portion of 1.08 M DIBALH in hexane (2 equiv.) was added dropwise under nitrogen atmosphere. The solution was stirred for 1 h at 0 oC. The reaction mixture was first diluted with chloroform (15 mL) followed by 34 mL of 10% HCl, and the solution was stirred at room temperature for another 1 h. The organic layer separated was washed with distilled water and dried over anhydrous Na2SO4. The solvent was almost completely removed from the filtrate under reduced pressure, and the residue was washed with ice-cold n-hexane and dried at 50 oC under vacuum to afford 4-(bromomethyl)benzaldehyde. Yield: 70%; 1 H NMR (300 MHz, CDCl3, TMS): δ = 10.02 (s, 1H), 7.86 (m, 2H), 7.57 (m, 2H), 4.52 (s, 2H) ppm[1].
References[1] Sandeep, Anjamkudy et al. “Supercoiled fibres of self-sorted donor–acceptor stacks: a turn-off/turn-on platform for sensing volatile aromatic compounds.” Chemical Science 7 (2016): 4460–4467.
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