249998
氯化钛(III) 溶液
~10 wt. % in 20-30 wt. % hydrochloric acid
别名:
三氯化钛
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关于此项目
线性分子式:
TiCl3
化学文摘社编号:
分子量:
154.23
UNSPSC Code:
12352301
PubChem Substance ID:
MDL number:
InChI
1S/3ClH.Ti/h3*1H;/q;;;+3/p-3
SMILES string
Cl[Ti](Cl)Cl
InChI key
YONPGGFAJWQGJC-UHFFFAOYSA-K
reaction suitability
reagent type: catalyst
core: titanium
concentration
~10 wt. % in 20-30 wt. % hydrochloric acid
density
1.192 g/mL at 25 °C
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Application
Catalyst for:
Hydrogen desorption properties
Nitrogen-nitrogen reductive bond cleavage
Reagent for:
Photocatalyst synthesis
Preparation of nanostructures titania/cetyltrimethyammonium bromide nanoskeleton
Hydrogen desorption properties
Nitrogen-nitrogen reductive bond cleavage
Reagent for:
Photocatalyst synthesis
Preparation of nanostructures titania/cetyltrimethyammonium bromide nanoskeleton
Other Notes
精确浓度见标签
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B - STOT SE 3
target_organs
Respiratory system
存储类别
8B - Non-combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
S. Isobe, et al.,
Applied Physics Letters, 99 (2011)
Shuxi Dai et al.
Nanoscale research letters, 5(11), 1829-1835 (2010-12-03)
Highly crystalline TiO(2) nanostructures were prepared through a facile inorganic acid-assisted hydrothermal treatment of hexagonal-structured assemblies of nanocrystalline titiania templated by cetyltrimethylammonium bromide (Hex-ncTiO(2)/CTAB Nanoskeleton) as starting materials. All samples were characterized by X-ray diffraction (XRD) and transmission electron microscopy
D. Meroni, et al
Catalysis Today, 161, 169-174 (2011)
Jun-ichi Matsuo et al.
Organic letters, 12(14), 3266-3268 (2010-06-24)
N-p-Toluenesulfonyl (Ts) aldimines reacted with 3-ethoxycyclobutanones by catalysis of titanium(IV) chloride to afford 2,3-di- or 2,3,3-trisubstituted N-Ts-2,3-dihydro-4-pyridones. Synthesis of (+/-)-bremazocine was efficiently accomplished by using this method.
Gema Ruano et al.
The Journal of organic chemistry, 68(5), 2024-2027 (2003-03-01)
Enantiomerically pure N-substituted epoxyalkene-2-azetidinones reacted with titanocene monochloride to give stereospecifically polyfunctionalized bicyclic beta-lactams. Four isomeric epoxyaldehydes 2 reacted with TiCp2Cl to give exclusively the respective carbacephams 7 while under the same reaction conditions the epoxyesters 1, which are more
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