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183431

Sigma-Aldrich

4-Bromophenethyl alcohol

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
Beilstein:
2079929
EC Number:
225-093-7
MDL number:
MFCD00002897
UNSPSC Code:
12352100
PubChem Substance ID:
24851052
NACRES:
NA.22

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.)

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

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Application

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

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

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’.

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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%
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
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

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