All Photos(1)
About This Item
Linear Formula:
FC6H4CH2OH
CAS Number:
Molecular Weight:
126.13
Beilstein:
2242511
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Recommended Products
Quality Level
Assay
98%
form
liquid
refractive index
n20/D 1.513 (lit.)
bp
104-105 °C/22 mmHg (lit.)
density
1.164 g/mL at 25 °C (lit.)
SMILES string
OCc1cccc(F)c1
InChI
1S/C7H7FO/c8-7-3-1-2-6(4-7)5-9/h1-4,9H,5H2
InChI key
QDHRSLFSDGCJFX-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
General description
3-Fluorobenzyl alcohol undergoes acetylation reaction with acetic anhydride catalyzed by tribromo melamine to yield 3-fluorobenzyl acetate.
Application
3-Fluorobenzyl alcohol was used as substrate to study pH dependence of aryl-alcohol oxidase activity.
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
194.0 °F - closed cup
Flash Point(C)
90 °C - closed cup
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Tribromo melamine as novel and versatile catalyst for the formylation and acetylation of alcohols.
Hajjami M, et al.
Chinese Journal of Catalysis, 35(2), 260-263 (2013)
Rianne E van Outersterp et al.
The Analyst, 145(18), 6162-6170 (2020-09-15)
Distinguishing positional isomers, such as compounds having different substitution patterns on an aromatic ring, presents a significant challenge for mass spectrometric analyses and is a frequently encountered difficulty in, for example, drug metabolism research. In contrast to mass spectrometry, IR
Patricia Ferreira et al.
The Journal of biological chemistry, 284(37), 24840-24847 (2009-07-04)
Aryl-alcohol oxidase (AAO) is a FAD-containing enzyme in the GMC (glucose-methanol-choline oxidase) family of oxidoreductases. AAO participates in fungal degradation of lignin, a process of high ecological and biotechnological relevance, by providing the hydrogen peroxide required by ligninolytic peroxidases. In
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service