vanadium(V) oxychloride
A
vanadium(II) oxide
B
vanadium oxychloride
C
vanadyl chloride
Conditions | Yield |
---|---|
In gas byproducts: Cl2; Irradiation (UV/VIS); irradiation of VOCl3 by pulsed CO2 laser radiation; detected by luminescence spectroscopy; |
vanadyl chloride
Conditions | Yield |
---|---|
With oxygen In not given | |
With O2 In not given |
vanadyl-p-toluene sulfinate
vanadyl chloride
Conditions | Yield |
---|---|
With hydrogenchloride In 1,4-dioxane |
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: VCl3, O2; 600-1000°C; |
Conditions | Yield |
---|---|
In solid heating in range 220-500°C; not isolated; |
Conditions | Yield |
---|---|
In ethanol at 25℃; for 1h; |
Conditions | Yield |
---|---|
In ethanol byproducts: NaCl; vacuum., mixing of alcoholic VOCl2 and soln. of NaO(i-Pr) in EtOH, room temp.; removal of pptd. NaCl (freezing, liquid N2), evapn. (ca. 40°C); elem. anal.; | 95% |
Conditions | Yield |
---|---|
In ethanol byproducts: NaCl; vacuum., mixing of alcoholic VOCl2 and soln. of NaOEt in EtOH, room temp.; removal of pptd. NaCl (freezing, liquid N2), evapn. (ca. 40°C); elem. anal.; | 95% |
4’-ferrocenyl-2,2’:6’,2’’-terpyridine
1,7-bis(3-methoxyphenyl)-1,6-heptadiene-3,5-dione
vanadyl chloride
Conditions | Yield |
---|---|
Stage #1: 1,7-bis(3-methoxyphenyl)-1,6-heptadiene-3,5-dione; vanadyl chloride With sodium hydroxide In water for 0.5h; Stage #2: 4’-ferrocenyl-2,2’:6’,2’’-terpyridine In methanol; chloroform; water for 0.5h; Stage #3: sodium perchlorate In methanol; chloroform; water | 80% |
Conditions | Yield |
---|---|
Stage #1: curcumin; vanadyl chloride With sodium hydroxide In water for 0.5h; Stage #2: 4'-phenyl-2,2':6',2-terpyridine In methanol; chloroform; water for 0.5h; Stage #3: sodium perchlorate In methanol; chloroform; water | 72% |
Conditions | Yield |
---|---|
Stage #1: curcumin; vanadyl chloride With sodium hydroxide In water for 0.5h; Stage #2: 4’-ferrocenyl-2,2’:6’,2’’-terpyridine In methanol; chloroform; water for 0.5h; Stage #3: sodium perchlorate In methanol; chloroform; water | 70% |
4’-ferrocenyl-2,2’:6’,2’’-terpyridine
bisdemethoxycurcumin
vanadyl chloride
Conditions | Yield |
---|---|
Stage #1: bisdemethoxycurcumin; vanadyl chloride With sodium hydroxide In water for 0.5h; Stage #2: 4’-ferrocenyl-2,2’:6’,2’’-terpyridine In methanol; chloroform; water for 0.5h; Stage #3: sodium perchlorate In methanol; chloroform; water | 68% |
vanadyl chloride
salicylaldehyde
2-Amino-2-methyl-1-propanol
VO(SALAHE)
Conditions | Yield |
---|---|
In ethanol to an ethanolic soln. of VOCl2 was added aldehyde and amine, the soln. was stirred for about 3 h at room temp., then allowed to stand overnight; filtered, recrystd. from 1,2-dichloroethane/hexane; elem. anal.; | 65% |
Conditions | Yield |
---|---|
With tetramethyl ammoniumhydroxide | 64.6% |
vanadyl chloride
Conditions | Yield |
---|---|
With oxygen In methanol for 12h; | 64% |
Conditions | Yield |
---|---|
With tetramethyl ammoniumhydroxide | 62.3% |
Conditions | Yield |
---|---|
With triethylamine In ethanol at 80℃; for 6h; | 61.02% |
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: carbon dioxide, hydrochloride; solid VOCl2 and thioacetic acid warmed to 60.edgree.C for 2 days; crystal filtered, washed with water and benzene and dried under vac.; elem. anal.; | 60% |
Conditions | Yield |
---|---|
With triethylamine In methanol; acetonitrile Heating; | 55% |
Conditions | Yield |
---|---|
In methanol for 0.25h; pH=5; Inert atmosphere; Schlenk technique; | 50% |
water
vanadyl chloride
sodium chloride
sodium hydroxide
sodium sulfite
Conditions | Yield |
---|---|
In hydrogenchloride High Pressure; aq. soln. of Na comps. slowly added to a soln. of V comp., enclosed, heated at 202°C for 3 d; cooled to room temp. (0.1°C/min), cryts. filtered, washed, dried (air); elem. anal.; | 22% |
vanadyl chloride
Conditions | Yield |
---|---|
In methanol; N,N-dimethyl-formamide soln. of ligand in DMF was added to MeOH soln. of VOCl2; heated at 50°C for 30 min with stirring;; filtered, water added to the hot filtrate; recrystn. by cooling (refrigerator); recrystn. from DMF; elem. anal.;; | 18% |
Conditions | Yield |
---|---|
Kinetics; 120-230°C; elem. anal.; |
vanadyl chloride
(N-hydroxyimino)diacetic acid
Conditions | Yield |
---|---|
In not given slow evapn.; |
vanadium(III) chloride
vanadyl chloride
A
vanadiumtetrachloride
B
vanadium(V) oxychloride
Conditions | Yield |
---|---|
200°C; |
phosphoric acid
vanadyl chloride
Conditions | Yield |
---|---|
In not given mixing of VOCl2 soln. with 70% H3PO4, boiling with reflux for 3 h, evapn. on a water-bath, heating at 200°C; content of V(4+) and V(5+) det. by titration with potassium permanganate and Mohr's salt, XRD, EPR; |
vanadyl chloride
Conditions | Yield |
---|---|
With CH3COOH; (CH3CO)2O In acetic acid in N2 atm. VOCl2 was refluxed with acetic acid containing acetic anhydride; elem. anal.; |
Conditions | Yield |
---|---|
In solid |
Conditions | Yield |
---|---|
pH=7; low-temp. drying; |
Conditions | Yield |
---|---|
pH=7; low-temp. drying; |
Conditions | Yield |
---|---|
pH=7; low-temp. drying; |
Conditions | Yield |
---|---|
pH=7; low-temp. drying; |
Chemical Name: Vanadium dichloride oxide
IUPAC NAME: Oxovanadium dihydrochloride
CAS No.: 10213-09-9
EINECS: 233-517-7
Molecular Formula: Cl2H2OV
Molecular Weight: 139.86 g/mol
Following is the structure of Dichlorooxovanadium (10213-09-9):
The chemical synonymous of Dichlorooxovanadium (10213-09-9) are Vanadium dichloride oxide ; Vanadium oxydichloride ; Vanadyl dichloride ; Vanadyloxychloride ; Vanadyloxydichloride ; Dichlorooxovanadium ; Dichlorooxo-vanadium ; Dichlorooxovanadium(Iv)
1. | mrc-bcs 400 mmol/L | MUREAV Mutation Research. 77 (1980),109. |
EPA Genetic Toxicology Program.
Mutation data reported. See also VANADIUM COMPOUNDS and CHLORIDES. Reacts violently with K. When heated to decomposition it emits toxic fumes of Cl− and VOx.
ACGIH TLV: TWA 0.05 mg(V2O5)/m3
NIOSH REL: (Vanadium Compounds) CL 0.05 mg(V)/m3/15M
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