Skip to Content
Merck
All Photos(1)

Documents

474819

Sigma-Aldrich

Benzyl 2-bromoethyl ether

97%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
C6H5CH2OCH2CH2Br
CAS Number:
Molecular Weight:
215.09
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

refractive index

n20/D 1.541 (lit.)

bp

254 °C (lit.)

density

1.36 g/mL at 25 °C (lit.)

SMILES string

BrCCOCc1ccccc1

InChI

1S/C9H11BrO/c10-6-7-11-8-9-4-2-1-3-5-9/h1-5H,6-8H2

InChI key

FWOHDAGPWDEWIB-UHFFFAOYSA-N

General description

Benzyl 2-bromoethyl ether is an organic building block. Its enthalpy of vaporization at boiling point (527.15K) has been reported to be 46.499kjoule/mol.

Application

Alkylation reagent for synthesis of a macrocyclic antifungal antibiotic.
Building block used to prepare a copper phthalocyanine discotic liquid crystal.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

>235.4 °F - closed cup

Flash Point(C)

> 113 °C - closed cup

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’.

Already Own This Product?

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

Visit the Document Library

680290
CorpBase ID (for auto-filling citation data) null
Chemistry of Materials, 17, 1618-1618 (2005)
Fodil Bouazza et al.
Organic letters, 5(22), 4049-4052 (2003-10-24)
[reaction: see text]. (-)-PF1163B, a new macrocyclic antifungal antibiotic isolated from Streptomyces sp., has been prepared in eight steps from (S)-citronellene. The key step is a ring-closing metathesis reaction of an ester and amide derivative obtained from a substituted N-methyl-l-tyrosine.

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