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About This Item
Empirical Formula (Hill Notation):
C5H3BrO2S
CAS Number:
Molecular Weight:
207.05
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
97%
mp
141-144 °C (lit.)
functional group
bromo
carboxylic acid
storage temp.
2-8°C
SMILES string
OC(=O)c1ccc(Br)s1
InChI
1S/C5H3BrO2S/c6-4-2-1-3(9-4)5(7)8/h1-2H,(H,7,8)
InChI key
COWZPSUDTMGBAT-UHFFFAOYSA-N
Application
5-Bromo-2-thiophenecarboxylic acid may be used in the preparation of:
- 5-bromo-2-thiophenecarboxylic acid butyl ester
- sulphonyl-tetrafluorophenyl (STP) esters
- new porphyrin sensitizers based on donor-Π-acceptor (D-Π-A) approach
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
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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THE SYNTHESIS AND CHARACTERIZATION OF AMPHIPHILIC a, a'-DISUBSTITUTED OLIGOTHIOPHENES.
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Lead is a heavy toxic metal element in biological systems and is one of the major pollutants as a result of its widespread use in industries. In spite of its negative roles the coordination chemistry of Pb(II) complexes is a
Effect of ester moieties in dye structures on photoinduced reorientation of dye-doped liquid crystals.
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This paper summarizes some of our results on the application of oligothiophenes as fluorescent markers for biological studies. The oligomers of thiophene, widely known for their semiconductor properties in organic electronics, are also fluorescent compounds characterized by chemical and optical
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New porphyrin sensitizers based on donor-π-acceptor (D-π-A) approach have been designed, synthesized, characterized by various spectroscopic techniques and their photovoltaic properties explored. N,N'-Diphenylamine acts as donor, the porphyrin is the π-spacer, and either carboxylic acid or cyanoacryclic acid acts as
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