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4-Bromobenzyl alcohol

ALDRICH/187054 - 99%

Synonym: (4-Bromophenyl)methanol; (p-Bromophenyl)methanol; 1-(p-Bromophenyl)methanol; 1-Bromo-4-(hydroxymethyl)benzene; 4-Hydroxymethyl-1-bromobenzene; p-Bromobenzyl alcohol

CAS Number: 873-75-6
Empirical Formula (Hill Notation): C7H7BrO
Molecular Weight: 187.03
EC Number: 212-851-7
MDL Number: MFCD00004650
Linear Formula: BrC6H4CH2OH
Product Type: Chemical
Catalog Number PKG Qty. Price Quantity
45-187054-10G 10 g
 $76.10
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45-187054-50G 50 g
 $191.00
1/EA		 Add To Favorites
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 187054-50G

 

assay 99%
form solid
InChI 1S/C7H7BrO/c8-7-3-1-6(5-9)2-4-7/h1-4,9H,5H2
InChI key VEDDBHYQWFOITD-UHFFFAOYSA-N
mp 75-77 °C (lit.)
Quality Level 100 
SMILES string OCc1ccc(Br)cc1
solubility dioxane: soluble 1 g/10 mL, clear to faintly turbid, colorless to faintly yellow
Application: 4-Bromobenzyl alcohol was used in the synthesis of:
• hydroxyl end functionalized, substituted polyfluorene
• amphiphilic, symmetric rod-coil, triblock copolymer of poly(9,9-didodecylfluorene-2,7-diyl) and poly(hydroxyl ethyl methacrylate)
General description: 4-Bromobenzyl alcohol undergoes three-component reaction with acetylferrocene and arylboronic acid to give ferrocenyl ketones containing biaryls. It undergoes oxidation reaction in the presence of polyvinylpolypyrrolidone-supported hydrogen peroxide, silica sulfuric acid and ammonium bromide to yield 4-bromobenzaldehyde. It undergoes efficient trimethylsilylation reaction with 1,1,1,3,3,3-hexamethyldisilazane in the presence of catalytic amount of aspartic acid in acetonitrile.
Packaging: 10, 50 g in glass bottle
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity 99%
mp 75-77 °C (lit.)
UNSPSC 12352100

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