Skip to Content
MilliporeSigma
All Photos(1)

Documents

528870

Sigma-Aldrich

5-Bromo-2-fluorobenzaldehyde

97%

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
BrC6H3(F)CHO
CAS Number:
93777-26-5
Molecular Weight:
203.01
EC Number:
298-056-6
MDL number:
MFCD00070755
UNSPSC Code:
12352100
PubChem Substance ID:
24877622
NACRES:
NA.22

assay

97%

refractive index

n20/D 1.57 (lit.)

bp

230 °C (lit.)

density

1.71 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

Fc1ccc(Br)cc1C=O

InChI

1S/C7H4BrFO/c8-6-1-2-7(9)5(3-6)4-10/h1-4H

InChI key

MMFGGDVQLQQQRX-UHFFFAOYSA-N

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

228.9 °F - closed cup

flash_point_c

109.4 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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

Christian Ruzié et al.
The Journal of organic chemistry, 78(15), 7741-7748 (2013-07-16)
The synthesis of 1,6-, 2,7-, 3,8-, and 4,9-isomers of dibromo- and didodecyl[1]benzothieno[3,2-b][1]benzothiophenes, via the stilbene pathway, is described. Starting from the synthesis of bromo-2-(methylthio)benzaldehydes, a series of functionalization, McMurry coupling, and finalising cyclization reactions were explored. The stereochemistry of the
Synthesis of 5-cyanoindazole and 1-methyl and 1-aryl-5-cyanoindazoles.
Halley F and Sava X.
Synthetic Communications, 27(7), 1199-1207 (1997)
High throughput synthesis of diverse 2, 5-disubstituted indoles using titanium carbenoids bearing boronate functionality.
Main CA, et al.
Tetrahedron, 64(5), 901-914 (2008)
Keith W Woods et al.
Bioorganic & medicinal chemistry, 14(20), 6832-6846 (2006-07-18)
A series of heteroaryl-pyridine containing inhibitors of Akt are reported. The synthesis and structure-activity relationships are discussed, leading to the discovery of a indazole-pyridine analogue (K(i)=0.16 nM). These compounds bind in the ATP binding site, are potent, ATP competitive, and

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