Skip to Content
Merck
All Photos(1)

Key Documents

B57206

Sigma-Aldrich

3-Bromobenzaldehyde

97%

Synonym(s):

3-Bromobenzaldehyde, 3-Formyl-1-bromobenzene, 3-Formylbromobenzene, 3-Formylphenyl bromide, 5-Bromobenzaldehyde, m-Bromobenzaldehyde, m-Formylphenyl bromide

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
BrC6H4CHO
CAS Number:
Molecular Weight:
185.02
Beilstein:
1634534
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

form

liquid

refractive index

n20/D 1.593 (lit.)

bp

233-236 °C (lit.)

mp

18-21 °C (lit.)

density

1.587 g/mL at 25 °C (lit.)

SMILES string

Brc1cccc(C=O)c1

InChI

1S/C7H5BrO/c8-7-3-1-2-6(4-7)5-9/h1-5H

InChI key

SUISZCALMBHJQX-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

204.8 °F - closed cup

Flash Point(C)

96 °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

Duyang Gao et al.
Theranostics, 9(18), 5315-5331 (2019-08-15)
Background: Engineering a single organic-molecule-based nanoparticle integrating precise diagnosis and effective therapy is of great significance for cancer treatment and future clinical applications but remains a great challenge. The goal of this study is to explore small organic molecule-based nanoparticles
[Determination of 3-bromobenzaldehyde, 3-phenoxybenzaldehyde and 3-phenoxybenzyl alcohol in the air of the work place].
N Ia Smoliar
Gigiena i sanitariia, (2)(2), 69-69 (1990-02-01)
Antara Garai et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 24(48), 12613-12622 (2018-06-09)
Metal- versus ligand-centered redox processes and the effects of substituents on the ligands on the spectroscopic properties of the metal complexes are at the heart of research on metal complexes with non-innocent ligands. This work presents three examples of chromium
J P Fernandez et al.
Journal of medicinal chemistry, 26(9), 1317-1319 (1983-09-01)
Molecular biotransformation of 2-phenylthiazolidine (1) and its m-bromo derivative (2) in the mouse is followed by autoradiographic studies and assessed by analysis of urinary metabolites. Cysteamine (4) is one of the metabolites of compounds 1 and 2. Radioprotective activity and
Subhasish Tapadar et al.
Bioorganic & medicinal chemistry, 23(24), 7543-7564 (2015-11-21)
Inhibition of the enzymatic activity of histone deacetylase (HDAC) is a promising therapeutic strategy for cancer treatment and several distinct small molecule histone deacetylase inhibitors (HDACi) have been reported. We have previously identified a new class of non-peptide macrocyclic HDACi

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