283452
4-Bromo-2-thiophenecarboxaldehyde
90%
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Empirical Formula (Hill Notation):
C5H3BrOS
CAS Number:
Molecular Weight:
191.05
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
242-577-3
Beilstein/REAXYS Number:
108455
MDL number:
Product Name
4-Bromo-2-thiophenecarboxaldehyde, 90%
InChI key
PDONIKHDXYHTLS-UHFFFAOYSA-N
InChI
1S/C5H3BrOS/c6-4-1-5(2-7)8-3-4/h1-3H
SMILES string
[H]C(=O)c1cc(Br)cs1
assay
90%
form
solid
bp
114-115 °C/11 mmHg (lit.)
mp
44-46 °C (lit.)
functional group
aldehyde
bromo
storage temp.
2-8°C
Quality Level
Looking for similar products? Visit Product Comparison Guide
Application
4-Bromo-2-thiophenecarboxaldehyde has been used:
- as building block for the synthesis of tetrahydroisoquinolinones
- in the synthesis of 3-[(4-bromo-2-thienyl)methylenehydrazinocarbonyl]-1H-1,2,4-triazole
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
3-[(4-Bromo-2-thienyl) methylenehydrazinocarbonyl]-1H-1, 2, 4-triazole.
Yang J-G and Pan F-Y.
Acta Crystallographica Section E, Structure Reports Online, 60(12), o2342-o2344 (2004)
M Lebl
Bioorganic & medicinal chemistry letters, 9(9), 1305-1310 (1999-05-26)
A new technique for high throughput solid phase synthesis using the centrifuge based liquid removal from readily available standard microtiterplates is described. This technique eliminates the filtration step and is therefore applicable to simultaneous processing of an unlimited number of
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