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About This Item
Linear Formula:
BrC6H3(F)CHO
CAS Number:
Molecular Weight:
203.01
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
97%
refractive index
n20/D 1.57 (lit.)
bp
230 °C (lit.)
density
1.71 g/mL at 25 °C (lit.)
functional group
aldehyde
bromo
fluoro
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
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
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)
228.9 °F - closed cup
Flash Point(C)
109.4 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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)
Synthesis of 5-cyanoindazole and 1-methyl and 1-aryl-5-cyanoindazoles.
Halley F and Sava X.
Synthetic Communications, 27(7), 1199-1207 (1997)
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
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 528870-25G | 4061836685751 |
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