Skip to Content
Merck
All Photos(1)

Documents

779318

Sigma-Aldrich

1-Azido-2-bromobenzene solution

~0.5 M in tert-butyl methyl ether

Synonym(s):

2-Bromophenyl azide solution

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C6H4BrN3
CAS Number:
Molecular Weight:
198.02
Beilstein:
1941487
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:

Assay

≥95.0% (HPLC)

form

solution

concentration

~0.5 M in tert-butyl methyl ether

impurities

≤2.0% water

storage temp.

−20°C

SMILES string

Brc1ccccc1N=[N+]=[N-]

InChI

1S/C6H4BrN3/c7-5-3-1-2-4-6(5)9-10-8/h1-4H

InChI key

QOVQEONXPGQIHT-UHFFFAOYSA-N

General description

1-Azido-2-bromobenzene is an aromatic azide generally used in copper(I)-catalyzed azide-alkyne cycloaddition reactions. It can also undergo palladium-catalyzed cross-coupling with arylboronic acids to form the corresponding azido-bis-aryl derivatives.

Application

Review

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT RE 1

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

-27.4 °F

Flash Point(C)

-33 °C


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

First Suzuki?Miyaura type cross-coupling of ortho-azidobromobenzene with arylboronic acids and its application to the synthesis of fused aromatic indole-heterocycles
Pudlo M, et al.
Tetrahedron, 63(41), 10320-10329 (2007)
Cu-catalyzed azide? alkyne cycloaddition
Meldal M & Torn?e CW
Chemical Reviews, 108(8), 2952-3015 (2008)
Stefan Bräse et al.
Angewandte Chemie (International ed. in English), 44(33), 5188-5240 (2005-08-16)
Since the discovery of organic azides by Peter Griess more than 140 years ago, numerous syntheses of these energy-rich molecules have been developed. In more recent times in particular, completely new perspectives have been developed for their use in peptide

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