467464
Thianaphthene-2-carboxylic acid
98%
Synonym(s):
Benzo[b]thiophene-2-carboxylic acid
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About This Item
Empirical Formula (Hill Notation):
C9H6O2S
CAS Number:
Molecular Weight:
178.21
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
98%
mp
241-244 °C (lit.)
SMILES string
OC(=O)c1cc2ccccc2s1
InChI
1S/C9H6O2S/c10-9(11)8-5-6-3-1-2-4-7(6)12-8/h1-5H,(H,10,11)
InChI key
DYSJMQABFPKAQM-UHFFFAOYSA-N
General description
Thianaphthene-2-carboxylic acid, a benzothiophene, is a heterocyclic sulfur compound. It undergoes degradation (23%) by employing a mixture of washed cells of Rhodococcus erythropolis DS-3 and Gordonia sp. C-6.
Application
Thianaphthene-2-carboxylic acid may be used for the fabrication of carboxylated conducting polymer/CNTs (carbon nanotubes) composites thin films.
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
Certificates of Analysis (COA)
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J C Robin et al.
Journal of medicine, 11(1), 15-27 (1980-01-01)
Total skeletal calcium was determined in female mice with the aid of whole body neutron activation analysis. Three months treatment with heaprin produced significant osteoporosis in C3-H/St(Ha) mice but not in C57/BL6(J) mice. This was more pronounced in the younger
M Nyska et al.
International journal of experimental pathology, 73(6), 733-740 (1992-12-01)
Thionaphthene-2-carboxylic acid (TNCA) has been shown to decrease osteoclast-mediated bone resorption in vitro and has shown efficacy in animal models of hypercalcaemia of malignancy. In this study, the effects of TNCA on the tibial proximal epiphysis and the sternum have
Fabrication of Carboxylated Conducting Polymer/CNTs Composites Thin Films for Immunosensor Application.
Netsuwan P, et al.
Mol. Cryst. Liq. Cryst., 580(1), 7-14 (2013)
The synthesis of some substituted thianaphthene-2-carboxamides and their antifungal properties.
Goettsch RW and Wiese GA.
Journal of the American Pharmaceutical Association, 47(5), 319-322 (1958)
Guo-Qiang Li et al.
Biotechnology letters, 30(10), 1759-1764 (2008-06-03)
Substituted benzothiophenes (BTs) and dibenzothiophenes (DBTs) remain in diesel oil following conventional desulfurization by hydrodesulfurization. A mixture of washed cells (13.6 g dry cell wt l(-1)) of Rhodococcus erythropolis DS-3 and Gordonia sp. C-6 were employed to desulfurize hydrodesulfurized diesel
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