跳转至内容
Merck

227609

Sigma-Aldrich

癸硼烷

white

别名:

十硼烷

登录查看公司和协议定价


About This Item

线性分子式:
B10H14
CAS号:
分子量:
122.22
EC號碼:
MDL號碼:
分類程式碼代碼:
12352000

蒸汽壓力

0.15 mmHg ( 20 °C)

品質等級

形狀

solid

反應適用性

reagent type: reductant

顏色

white

bp

213 °C (lit.)

mp

98-100 °C (lit.)

密度

0.94 g/mL at 25 °C (lit.)

正在寻找类似产品? 访问 产品对比指南

應用

Reactant for:
  • Chemical vapor deposition of boron nitride nanosheets on Ni or Cu foils in the presence of ammonia
  • Stereoselective catalytic hydrogenation reactions
  • Chemical hydrogen storage
  • Preparation of carborane-conjugated quinoline carboxamide ligands of translocator protein for boron neutron capture therapy (BNCT)
  • Synthesis of hydrogenated boron clusters B12Hn with controlled hydrogen content
  • Preparation of alkenyldecaboranes by regioselective transition-metal-catalyzed decaborane-alkyne hydroboration reactions
用于离子注入工艺的硼源

象形圖

FlameSkull and crossbones

訊號詞

Danger

危險分類

Acute Tox. 2 Inhalation - Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Eye Irrit. 2 - Flam. Sol. 1 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

4.1B - Flammable solid hazardous materials

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges, type P3 (EN 143) respirator cartridges


从最新的版本中选择一种:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

Kiminori Ohta et al.
Bioorganic & medicinal chemistry letters, 14(23), 5913-5918 (2004-10-27)
We designed and synthesized novel retinoid X receptor (RXR)-selective antagonists bearing a carborane moiety. Compounds 8a-d or 9a-d themselves have no differentiation-inducing activity toward HL-60 cells and no inhibitory activity towards a retinoic acid receptor (RAR) agonist. However, they inhibit
Zhu Yinghuai et al.
Journal of the American Chemical Society, 129(20), 6507-6512 (2007-05-03)
Well dispersed ruthenium(0) nanoparticles, stabilized in the ionic liquid agent, trihexyltetradecylphosphonium dodecylbenzenesulfonate, have been successfully prepared via a reduction reaction of the precursor [CpRuCp*RuCp*]PF6 (Cp* = C5Me5). The ruthenium(0) nanoparticles were shown to catalyze the isotope exchange reaction between 10B
Ilias Sioutis et al.
The journal of physical chemistry. A, 110(45), 12528-12534 (2006-11-10)
The interaction of decaborane (B(10)H(14)) with the I(-) ion and the (isoelectronic) Xe atom is investigated using a number of theoretical methods: MP2, CCSD(T), CCSD, spin-orbit CISD, and DFT using the B3LYP, B3PW91, PW91PW91, and PBE0 methods. All non-DFT and
Yuqi Li et al.
Inorganic chemistry, 47(20), 9193-9202 (2008-09-20)
Unlike in conventional organic solvents, where Lewis base catalysts are required, decaborane dehydrogenative alkyne-insertion reactions proceed rapidly in biphasic ionic-liquid/toluene mixtures with a wide variety of terminal and internal alkynes, thus providing efficient, one-step routes to functional o-carborane 1-R-1,2-C2B10H11 and

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门