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About This Item
Linear Formula:
MoCl5
CAS Number:
Molecular Weight:
273.21
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12352302
MDL number:
Assay:
95%
Form:
powder
Product Name
Molybdenum(V) chloride, 95%
InChI
1S/5ClH.Mo/h5*1H;/q;;;;;+5/p-5
SMILES string
Cl[Mo](Cl)(Cl)(Cl)Cl
InChI key
GICWIDZXWJGTCI-UHFFFAOYSA-I
vapor pressure
1.75 mmHg ( 25 °C)
131 mmHg ( 250 °C)
assay
95%
form
powder
reaction suitability
core: molybdenum
reagent type: catalyst
impurities
<0.5% insoluble matter
bp
268 °C (lit.)
mp
194 °C (lit.)
density
2.928 g/mL at 25 °C (lit.)
Quality Level
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Application
Molybdenum(V) chloride can be used as an efficient catalyst for:
It can also be used as aprecursor to synthesize alumina/molybdenum nanocomposites and methylenemolybdenumreagents for chemoselective carbonyl alkenation.
- Condensation of nitrobenzene with alcohols and C-C coupling of alkenyllithium reagents.
- Direct amidation of benzylic alcohols with sulfonamides and carbamates.
It can also be used as aprecursor to synthesize alumina/molybdenum nanocomposites and methylenemolybdenumreagents for chemoselective carbonyl alkenation.
General description
Molybdenum(V)chloride is a Lewis acid widely used as a catalyst and reagent in many organicreactions. It can be prepared by direct chlorination of molybdenum metal or byrefluxing thionyl chloride and MoO3.
signalword
Danger
hcodes
Hazard Classifications
Carc. 2 - Eye Dam. 1 - Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
危险化学品
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Kristina Hackeloer et al.
Organic letters, 13(5), 916-919 (2011-02-02)
A domino sequence involving various MoCl(5)-mediated oxidations followed by trapping and supposed [3,3]-sigmatropic rearrangement provides a fast access to the full carbon skeleton of metasequirin-B. A variety of different moieties R(1) and R(2) are tolerated.
Mladen Litvić et al.
Bioorganic & medicinal chemistry letters, 22(11), 3676-3681 (2012-05-02)
Mo(VI) and Mo(V) salts both react selectively with Hantzsch esters to produce substitute pyridines in good-to-excellent yield (75-99%). The remarkable reactivity and selectivity of MoOCl(4) under reflux of acetonitrile and MoCl(5) in dichloromethane at room temperature encouraged us to propose
Kumar, S. Manickam, M.
Chemical Communications (Cambridge, England), 1615-1615 (1997)
H I Ogawa et al.
Mutation research, 320(1-2), 133-140 (1994-01-01)
A series of metal chlorides were subjected to the wing spot test of Drosophila melanogaster. In the test, larvae trans-heterozygous for the wing-hair mutations mwh and flr were orally treated at the third instar stage with a test compound and
Simon Trosien et al.
Organic letters, 14(12), 2976-2979 (2012-06-05)
The strong oxidative power of molybdenum pentachloride gives rise to an efficient oxidative C-C bond formation of benzil derivatives to the corresponding 9,10-phenanthrenequinones. A highly complementary method to previous approaches was developed. The required derivatives are accessible in a modular
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