288187
o-Carborane
98%
Sinonimo/i:
1,2-Dicarbadodecaborane(12)
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About This Item
Formula empirica (notazione di Hill):
C2H12B10
Numero CAS:
Peso molecolare:
144.23
Numero CE:
Numero MDL:
Codice UNSPSC:
12352300
ID PubChem:
NACRES:
NA.23
Prodotti consigliati
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Saggio
98%
Punto di fusione
260 °C (subl.) (lit.)
Temperatura di conservazione
2-8°C
Stringa SMILE
[bH]1[bH][bH][bH][bH][bH]cc[bH][bH][bH][bH]1
InChI
1S/C2H12B10/c1-2-4-6-8-10-12-11-9-7-5-3-1/h1-12H/b2-1-
PWHTZDUTEHXWHV-UPHRSURJSA-N
Categorie correlate
Descrizione generale
Electron deficient boron cage compounds with one or more carbon atoms as a ligand in the borane framework. The three common isomers are o-carborane, m-carborane and p-carborane 1The structure could be polyhedral or open cage.
Confezionamento
Packaged in glass bottles
Avvertenze
Warning
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral
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
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Yin-Ping Wang et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 23(8), 1814-1819 (2016-11-30)
Palladium(II)-induced selective B(4)-H activation of an o-carboranylthioamide has been developed. A tetranuclear palladium(II) complex has been obtained in high yield with excellent regioselectivity. DFT calculations have confirmed that the B(4)-borometalate is lower in energy than the corresponding B(3)-borometalate. The product
Temidayo O B Olusanya et al.
Biophysical chemistry, 247, 25-33 (2019-02-24)
Based on the promise of liposomes as convenient vehicles for the transport of boronated agents for the boron neutron capture therapy (BCNT) of cancer, this paper reports a method for the formulation and characterisation of stable o-carborane-loaded liposomes (ca. 80-100 nm)
Issei Takeuchi et al.
Colloids and surfaces. B, Biointerfaces, 159, 360-365 (2017-08-15)
Poly(DL-lactide-co-glycolide) (PLGA) has been widely used and studied because of its biocompatibility and biodegradability. Recently, the usefulness of nanoparticles using poly(L-lactide-co-glycolide) (PLLGA) having a higher glass transition temperature than PLGA was suggested. In this study, we investigated the availability of
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