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Safety Information

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

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

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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

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

183431-10G:
183431-BULK:
183431-1G:
183431-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
SHBJ6034
SHBG6871V
SHBB1594V
40396PK
03497JJ

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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%
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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