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162507

Sigma-Aldrich

3-Fluorobenzyl alcohol

98%

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5 G
¥4,300

¥4,300

Available to ship onApril 15, 2025Details

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5 G
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About This Item

Linear Formula:
FC6H4CH2OH
CAS Number:
456-47-3
Molecular Weight:
126.13
Beilstein:
2242511
EC Number:
207-265-3
MDL number:
MFCD00004631
UNSPSC Code:
12352100
PubChem Substance ID:
24849986
NACRES:
NA.22

¥4,300

Available to ship onApril 15, 2025Details

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Quality Level

100

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.)

functional group

fluoro
hydroxyl

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

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General description

3-Fluorobenzyl alcohol undergoes acetylation reaction with acetic anhydride catalyzed by tribromo melamine to yield 3-fluorobenzyl acetate[1].

Application

3-Fluorobenzyl alcohol was used as substrate to study pH dependence of aryl-alcohol oxidase activity[2].

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

194.0 °F - closed cup

Flash Point(C)

90 °C - closed cup

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

162507-25G:
162507-BULK:
162507-5G:
162507-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
0000372265
0000316434
MKCW3643
0000372265
MKCW4072

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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

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