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183431

4-Bromophenethyl alcohol

Name: 4-Bromophenethyl alcohol
Brand: ALDRICH

99%

Synonym(s):

2-(4-Bromophenyl)ethanol

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About This Item

Linear Formula:

BrC₆H₄CH₂CH₂OH

CAS Number:

4654-39-1

Molecular Weight:

201.06

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24851052

EC Number:

225-093-7

Beilstein/REAXYS Number:

2079929

MDL number:

MFCD00002897

Assay:

99%

Form:

liquid

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Properties

Quality Level

200

assay

99%

form

liquid

refractive index

n20/D 1.573 (lit.)

bp

138 °C/9 mmHg (lit.)

density

1.436 g/mL at 25 °C (lit.)

functional group

bromo, hydroxyl

SMILES string

OCCc1ccc(Br)cc1

InChI

1S/C8H9BrO/c9-8-3-1-7(2-4-8)5-6-10/h1-4,10H,5-6H2

InChI key

PMOSJSPFNDUAFY-UHFFFAOYSA-N

Description

Application

4-Bromophenethyl alcohol was used in the synthesis of 4-(4-(3-(trifluoromethyl)-3H-diazirin-3-yl)phenethoxy)quinazoline.

pictograms

GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

10 - Combustible liquids

wgk

WGK 2

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Insecticidal quinazoline derivatives with (trifluoromethyl)diazirinyl and azido substituents as NADH:ubiquinone oxidoreductase inhibitors and candidate photoaffinity probes.

B Latli et al.

Chemical research in toxicology, 9(2), 445-450 (1996-03-01)

Two candidate photoaffinity probes are designed from 4-substituted quinazolines known to be potent insecticides/acaricides and NADH:ubiquinone oxidoreductase inhibitors acting at or near the rotenone site. 4-(11-Azidoundecyl-2-amino)quinazoline, based on the undecylamino analog SAN 548A as a prototype, was synthesized in 18%

One-Pot Synthesis of Thiol-Modified Liquid Crystals Conjugated Fluorescent Gold Nanoclusters.

Po-Hsuan Hsu et al.

Nanomaterials (Basel, Switzerland), 10(9) (2020-09-10)

Gold nanoclusters (AuNCs) and liquid crystals (LCs) have shown great potential in nanobiotechnology applications due to their unique optical and structural properties. Herein, the hardcore of the 4-cyano biphenyl group for commonly used LCs of 4-cyano-4'-pentylbiphenyl (5CB) was utilized to

Suitable in-situ derivatization of alcohols by reaction with basic amines in Direct Analysis in Real Time mass spectrometry.

Roman S Borisov et al.

Talanta, 200, 31-40 (2019-05-01)

This work highlights the discovered in-situ analytical reaction between primary/secondary alcohols and nitrogenous bases (pyridine, quinoline) that involves the substitution of hydroxyl groups for nitrogen-containing charged species and proceeds in an ionization region of Direct Analysis in Real Time mass

Global Trade Item Number

SKU	GTIN
183431-10G	04061837632280
183431-1G	04061837632297