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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

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About This Item

Linear Formula:
BrC6H4CHO
CAS Number:
3132-99-8
Molecular Weight:
185.02
Beilstein:
1634534
EC Number:
221-526-9
MDL number:
MFCD00003345
UNSPSC Code:
12352100
PubChem Substance ID:
24891855
NACRES:
NA.22

Quality Level

100

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

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319,H335

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

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Certificates of Analysis (COA)

Lot/Batch Number
STBK3626
STBJ0631
STBF1684V
STBD3290V
STBD0904V

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[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)
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
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
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
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
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