Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

183431

Sigma-Aldrich

4-Bromophenethyl alcohol

99%

Synonym(s):

2-(4-Bromophenyl)ethanol

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
BrC6H4CH2CH2OH
CAS Number:
4654-39-1
Molecular Weight:
201.06
Beilstein:
2079929
EC Number:
225-093-7
MDL number:
MFCD00002897
UNSPSC Code:
12352100
PubChem Substance ID:
24851052
NACRES:
NA.22
form:
liquid
Assay:
99%
Pricing and availability is not currently available.

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

Looking for similar products? Visit Product Comparison Guide

Application

4-Bromophenethyl alcohol was used in the synthesis of 4-(4-(3-(trifluoromethyl)-3H-diazirin-3-yl)phenethoxy)quinazoline[1].

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
SHBJ6034
SHBG6871V
SHBB1594V
40396PK
03497JJ

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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%
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
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

Questions

Reviews

No rating value

Active Filters

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