1,10-phenanthroline hydrochloride
Conditions | Yield |
---|---|
In water from aq. soln. of CuCl2 and soln. of phenanthroline hydrochloride in 2:1, 1:1 molar ratio at pH 6.5 maintained by an alkali soln.; solvent evapd. in a water bath; ppt. washed (H2O); dried (air); elem. anal.; | 96% |
1,10-phenanthroline hydrochloride
Conditions | Yield |
---|---|
In water from aq. soln. of CuCl2 and soln. of phenanthroline hydrochloride in 1:2, 1:3 molar ratio at pH 6.5 maintained by an alkali soln.; solvent evapd. in a water bath; ppt. washed (H2O); dried (air); elem. anal.; | 90% |
1,10-phenanthroline hydrochloride
bis(trifluoromethane)sulfonimide lithium
C2HF6NO4S2*C12H8N2
Conditions | Yield |
---|---|
With water at 20℃; for 2h; | 90% |
Conditions | Yield |
---|---|
In methanol for 1h; | 88% |
potassium permanganate
water
1,10-phenanthroline hydrochloride
copper
Conditions | Yield |
---|---|
In methanol byproducts: Mn(2+); stirring 1:1:2:2 mixt. of copper, permanganate salt, phenanthroline deriv., NH4Cl in methanol at 50-60°C in air for 2 h; addn. of isopropanol, isolation of crystals, elem. anal.; | 87% |
potassium permanganate
1,10-phenanthroline hydrochloride
copper
N,N-dimethyl-formamide
Conditions | Yield |
---|---|
In methanol; N,N-dimethyl-formamide byproducts: Mn(2+); stirring 1:1:2:2 mixt. of copper, permanganate salt, phenanthroline deriv., NH4Cl in methanol and DMF at 50-60°C in air for 2 h; addn. of isopropanol, isolation of crystals, elem. anal.; | 82% |
1,10-phenanthroline hydrochloride
Conditions | Yield |
---|---|
In methanol; water; butan-1-ol dissolving of amine hydrochloride in water, addn. of the phosphine-complex in methanol-butanol; filtn. after 10-15 min, washing (methanol), drying at room temp. in air, elem. anal.; | 72% |
1,10-phenanthroline hydrochloride
nitridoperoxo 1,10-phenanthroline technetium(VII)
Conditions | Yield |
---|---|
elem. anal.; | 70% |
1,10-phenanthroline hydrochloride
Conditions | Yield |
---|---|
In water dissolving of amine hydrochloride in water, addn. of Cr complex; addn. of methanol-butanol, filtn. after 10-15 min, washing (methanol), drying at room temp. in air, elem. anal.; | 65% |
1,10-phenanthroline hydrochloride
Conditions | Yield |
---|---|
In water under anaerobic conditions; water soln. of ligand (1 equiv.) added slowly to aq. soln. of V complex; left to stand for 4 d; crystals collected; elem. anal.; | 53% |
1,10-phenanthroline hydrochloride
A
3-bromophenanthroline
B
3,8-dibromo-1,10-phenathroline
Conditions | Yield |
---|---|
With bromine In nitrobenzene at 130 - 140℃; for 3h; | A 33% B 17% |
With water; bromine In nitrobenzene | |
With bromine In bromobenzene at 135℃; for 36h; |
1,10-phenanthroline hydrochloride
3-bromophenanthroline
Conditions | Yield |
---|---|
With bromine In nitrobenzene | 26% |
With bromine | 26% |
1,10-phenanthroline hydrochloride
3-anisyl-1,10-phenanthroline
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 26 percent / Br2 / nitrobenzene View Scheme |
1,10-phenanthroline hydrochloride
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 26 percent / Br2 / nitrobenzene 2: 20 percent / diethyl ether View Scheme |
1,10-phenanthroline hydrochloride
2-mesityl-8-anisyl-1,10-phenanthroline
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 26 percent / Br2 / nitrobenzene 2: 26 percent / diethyl ether View Scheme |
4-chloro-9,10-dihydro-9,10-dioxo-1-anthracenecarboxylic acid
1,10-phenanthroline hydrochloride
1-chloroanthracene-9,10-dione
Conditions | Yield |
---|---|
With 1-methyl-pyrrolidin-2-one In sulfuric acid; water |
tris(acetylacetonato)vanadium(III)
water
1,10-phenanthroline hydrochloride
[(V(o-phenanthroline)2Cl)2O](2+)
Conditions | Yield |
---|---|
In methanol reflux in MeOH; |
Conditions | Yield |
---|---|
In water prepn. from aq. dispersion of MoS2 and aq. soln. of 1,10-phenanthroline hydrochloride according to A. S. Golub et al., Solid State Ionics, 1996,vol. 91, p. 307; elem. anal.; |
Conditions | Yield |
---|---|
In water prepn. from aq. dispersion of MoS2 and aq. soln. of 1,10-phenanthroline hydrochloride according to A. S. Golub et al., Solid State Ionics, 1996,vol. 91, p. 307; elem. anal.; |
Conditions | Yield |
---|---|
In water mixing the aq. soln. of the ligand with the metal perchlorate soln. in at least 500-fold excess; not sepd., detected in soln. by UV/VIS; |
1,10-phenanthroline hydrochloride
[Zn-1,10-phenanthroline](2+)
Conditions | Yield |
---|---|
In water mixing the aq. soln. of the ligand with the metal perchlorate soln. in at least 500-fold excess; not sepd., detected in soln. by UV/VIS; |
1,10-phenanthroline hydrochloride
Conditions | Yield |
---|---|
With dichromate anion In water heating to about 80°C; | |
With Mn(2+) salt; Cr2O7(2-) In water heating to about 80°C; |
1,10-phenanthroline hydrochloride
Conditions | Yield |
---|---|
In water stirred; ppt. is washed (water, ethanol), dried under vac., elem. anal.; |
1,10-phenanthroline hydrochloride
[Ni(1,10-phenanthroline)](2+)
Conditions | Yield |
---|---|
In water mixing the aq. soln. of the ligand with the metal perchlorate soln. in at least 500-fold excess; not sepd., detected in soln. by UV/VIS; |
nitrosyltrichlororhenium
1,10-phenanthroline hydrochloride
Conditions | Yield |
---|---|
With KSCN In water the Re-complex is dissolved in a soln. of KSCN; mixt. refluxed for 15 min; phenanthrolinium hydrochloride added dropwise and with stirring; ppt. changes to oily drops at water-bath temp., mother liquor is separated, oil is repeatedly washed and dried under vac., elem. anal.; |
Conditions | Yield |
---|---|
In ethanol; water L-proline in H2O added to freshly prepared Cu(OH)2, C12H8N2*HCl in ethanol added with gentle warming; residue removed, soln. concd. under reduced pressure, crystd., elem. anal.; |
Conditions | Yield |
---|---|
In water at pH 6; not isolated; monitored by UV; |
aquo nitrosyldihydroxo oxalato rhenic acid
1,10-phenanthroline hydrochloride
1,10-phenanthroline nitrosylchloro oxalato rhenium
Conditions | Yield |
---|---|
In water refluxing a soln. of the rhenium complex acid and 1,10-phenanthroline hydrochloride for 3 h; filtn., washing with water and ethanol, drying in vacuo, elem. anal.; |
1,10-phenanthroline hydrochloride
(1,10-phenanthroline)manganese(II)
Conditions | Yield |
---|---|
In water mixing the aq. soln. of the ligand with the metal perchlorate soln. in at least 500-fold excess; not sepd., detected in soln. by UV/VIS; |
The Molecular Structure of 1,10-Phenanthroline, hydrochloride (1:1) (CAS NO.3829-86-5):
Empirical Formula: C12H9ClN2
Molecular Weight: 216.6663
IUPAC: 1,10-phenanthroline hydrochloride
Nominal Mass: 216 Da
Average Mass: 216.6663 Da
Monoisotopic Mass: 216.045426 Da
Flash Point: 164.8 °C
Enthalpy of Vaporization: 58.73 kJ/mol
Boiling Point: 365.1 °C at 760 mmHg
Melting Point: 224-225 °C(lit.)
Solubility H2O: 0.1 g/mL, clear
Water Solubility: soluble
BRN: 4007967
Appearance: white to light yellow or slightly purple powder
Vapour Pressure: 3.38E-05 mmHg at 25°C
InChI
InChI=1/C12H8N2.ClH/c1-3-9-5-6-10-4-2-8-14-12(10)11(9)13-7-1;/h1-8H;1H
Smiles
c12c3ncccc3ccc2cccn1.Cl
Product Categories: Aromatic Hydrocarbons (substituted) & Derivatives;Heterocyclic Compounds;Analytical Chemistry;Chelating Reagents;Phenanthrolines
Hazard Codes: TN
Risk Statements: 25-50/53
R25 :Toxic if swallowed
R50/53:Very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment
Safety Statements: 45-60-61
S45:In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
S60:This material and its container must be disposed of as hazardous waste
S61:Avoid release to the environment. Refer to special instructions / safety data sheets
RIDADR UN: 2811 6.1/PG 3
WGK Germany: 3
F 8:Photosensitive
HazardClass: 6.1
PackingGroup :III
1,10-Phenanthroline, hydrochloride (1:1) (CAS NO.3829-86-5) is also called as 1,10-Diazaphenanthrene hydrochloride ; 1,10-Phenanthroline hydrochloride ; EINECS 223-325-1 ; NSC 4265 ; Phenanthroline hydrochloride ; 1,10-Phenanthroline monohydrochloride monohydrate ; 1,10-Phenanthroline, monohydrochloride .
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