467464
Thianaphthene-2-carboxylic acid
98%
Sinonimo/i:
Benzo[b]thiophene-2-carboxylic acid
Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali
About This Item
Formula empirica (notazione di Hill):
C9H6O2S
Numero CAS:
Peso molecolare:
178.21
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
![Methyl benzo[b]thiophene-2-carboxylate 97%](/deepweb/assets/sigmaaldrich/product/structures/216/435/32affee2-b18f-4b51-a4fc-fd77f1af231c/640/32affee2-b18f-4b51-a4fc-fd77f1af231c.png)
Livello qualitativo
Saggio
98%
Punto di fusione
241-244 °C (lit.)
Gruppo funzionale
carboxylic acid
Stringa SMILE
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)
DYSJMQABFPKAQM-UHFFFAOYSA-N
Categorie correlate
Descrizione generale
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.
Applicazioni
Thianaphthene-2-carboxylic acid may be used for the fabrication of carboxylated conducting polymer/CNTs (carbon nanotubes) composites thin films.
Avvertenze
Warning
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Organi bersaglio
Respiratory system
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
Scegli una delle versioni più recenti:
Possiedi già questo prodotto?
I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.
I clienti hanno visto anche
![Benzo[b]thiophene-2-carboxaldehyde 97%](/deepweb/assets/sigmaaldrich/product/structures/321/060/32405a4e-5720-4c6d-91cf-115c747270c4/640/32405a4e-5720-4c6d-91cf-115c747270c4.png)
J C Robin et al.
Calcified tissue international, 36(2), 194-199 (1984-03-01)
The purpose of the present study was to investigate the mechanism of action on bone of Benzo(B)Thiophene-2-Carboxylic Acid (BL-5583). BL-5583, at a dose range of 0.01-100 micrograms/ml, inhibited spontaneous as well as A23187 and PTH-induced bone resorption in tissue culture.
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
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)
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)
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
Il team dei nostri ricercatori vanta grande esperienza in tutte le aree della ricerca quali Life Science, scienza dei materiali, sintesi chimica, cromatografia, discipline analitiche, ecc..
Contatta l'Assistenza Tecnica.