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4-Bromobenzyl alcohol

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4-Bromobenzyl alcohol Basic information

Product Name:
4-Bromobenzyl alcohol
Synonyms:
  • 4-BROMOBENZYL ALCOHOL
  • RARECHEM AL BD 0075
  • P-BROMOBENZYL ALCOHOL
  • (4-Bromophenyl)methanol
  • Benzyl alcohol, p-bromo-
  • 4-Brom-benzyl alcohol
  • Brombenzylalcohol
  • Benzenemethanol, 4-bromo-
CAS:
873-75-6
MF:
C7H7BrO
MW:
187.03
EINECS:
212-851-7
Product Categories:
  • Oxygen Compounds
  • Benzhydrols, Benzyl & Special Alcohols
  • Alcohol
  • Alcohols
  • Bromine Compounds
  • C7 to C8
Mol File:
873-75-6.mol
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4-Bromobenzyl alcohol Chemical Properties

Melting point:
75-77 °C (lit.)
Boiling point:
220.79°C (rough estimate)
Density 
1.3839 (rough estimate)
vapor pressure 
0.083Pa at 20℃
refractive index 
1.5840 (estimate)
storage temp. 
Sealed in dry,Room Temperature
solubility 
dioxane: soluble1g/10 mL, clear to faintly turbid, colorless to faintly yellow
pka
14.16±0.10(Predicted)
form 
Crystals or Crystalline Powder
color 
White to slightly beige
Water Solubility 
2.31g/L at 20℃
BRN 
1931620
InChIKey
VEDDBHYQWFOITD-UHFFFAOYSA-N
LogP
1.59 at 20℃
CAS DataBase Reference
873-75-6(CAS DataBase Reference)
NIST Chemistry Reference
Benzenemethanol, 4-bromo-(873-75-6)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
24/25
WGK Germany 
3
Hazard Note 
Irritant
HS Code 
29062990

MSDS

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4-Bromobenzyl alcohol Usage And Synthesis

Chemical Properties

WHITE TO SLIGHTLY BEIGE CRYSTALS OR CRYST. POWDER

Uses

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)

Synthesis Reference(s)

The Journal of Organic Chemistry, 48, p. 3074, 1983 DOI: 10.1021/jo00166a029
Tetrahedron Letters, 36, p. 3169, 1995 DOI: 10.1016/0040-4039(95)00504-6

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.

Flammability and Explosibility

Not classified

4-Bromobenzyl alcohol Preparation Products And Raw materials

Raw materials

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