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3-Fluorobenzyl alcohol

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3-Fluorobenzyl alcohol Basic information

Product Name:
3-Fluorobenzyl alcohol
Synonyms:
  • (3-Fluorophenyl)methanol
  • Benzyl alcohol, m-fluoro-
  • 3-FLUOROBENZYL ALCOHOL
  • 3-Fluorobenzylalcohol,98%
  • RARECHEM AL BD 0054
  • M-FLUOROBENZYL ALCOHOL
  • Benzenemethanol, 3-fluoro-
  • 3-Fluorobenzyl alcohol 98%
CAS:
456-47-3
MF:
C7H7FO
MW:
126.13
EINECS:
207-265-3
Product Categories:
  • Aryl Fluorinated Building Blocks
  • Building Blocks
  • C7 to C8
  • C7-C8
  • Chemical Synthesis
  • Fluorinated Building Blocks
  • Organic Building Blocks
  • Organic Fluorinated Building Blocks
  • Other Fluorinated Organic Building Blocks
  • Oxygen Compounds
  • Alcohol
  • Alcohols
  • Fluorine Compounds
  • C7 to C8
  • Oxygen Compounds
  • Benzhydrols, Benzyl & Special Alcohols
Mol File:
456-47-3.mol
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3-Fluorobenzyl alcohol Chemical Properties

Melting point:
115-119 °C
Boiling point:
104-105 °C/22 mmHg (lit.)
Density 
1.164 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.513(lit.)
Flash point:
195 °F
storage temp. 
Sealed in dry,Room Temperature
solubility 
Chloroform (Slightly), Methanol (Slightly)
pka
14.09±0.10(Predicted)
form 
Liquid
Specific Gravity
1.164
color 
Clear colorless
BRN 
2242511
CAS DataBase Reference
456-47-3(CAS DataBase Reference)
NIST Chemistry Reference
Benzenemethanol, 3-fluoro-(456-47-3)
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Safety Information

Hazard Codes 
Xi,C
Risk Statements 
14-34-36/37
Safety Statements 
24/25-45-36/37/39-27-26
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29062900

MSDS

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3-Fluorobenzyl alcohol Usage And Synthesis

Chemical Properties

clear colorless liquid

Uses

3-Fluorobenzyl alcohol was used as substrate to study pH dependence of aryl-alcohol oxidase activity.

Definition

ChEBI: 3-fluorobenzyl alcohol is a member of the class of benzyl alcohols that is benzyl alcohol substituted by a fluoro group at position 3. It is a member of monofluorobenzenes and a member of benzyl alcohols.

General Description

3-Fluorobenzyl alcohol undergoes acetylation reaction with acetic anhydride catalyzed by tribromo melamine to yield 3-fluorobenzyl acetate.

Synthesis

456-48-4

456-47-3

GENERAL STEPS: Prior to use, 0.05 g of 5 wt% Pt/C catalyst was pretreated in a stream of hydrogen at 673 K for 2 hours. Subsequently, the pretreated catalyst was mixed with 20 mL of solvent (e.g., ethanol) and the mixture was transferred to a 100 mL high-pressure reactor. After filling the reactor with hydrogen at 4.0 MPa, the reaction was initiated and hydrogenation was carried out at a set temperature. The reaction was terminated after reaching a predetermined time, and the products were analyzed by a gas chromatograph (GC-2014, Shimadzu Co.) equipped with a capillary column (DM-WAX, 30 m × 0.32 mm × 0.25 μm) coupled with a flame ionization detector (FID).

References

[1] Tetrahedron Letters, 1991, vol. 32, # 9, p. 1199 - 1202
[2] Organic Letters, 2007, vol. 9, # 15, p. 2791 - 2793
[3] Tetrahedron, 2008, vol. 64, # 51, p. 11783 - 11788
[4] Advanced Synthesis and Catalysis, 2014, vol. 356, # 5, p. 1093 - 1097
[5] Organic Letters, 2007, vol. 9, # 26, p. 5429 - 5432

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