2,2',4-trimethoxybenzophenone
(2-hydroxy-4-methoxyphenyl)(2-hydroxyphenyl)-methanone
Conditions | Yield |
---|---|
With hydrogen bromide; acetic acid at 110℃; Temperature; | 85% |
Conditions | Yield |
---|---|
With dipotassium peroxodisulfate; palladium diacetate; trifluoroacetic acid; trifluoroacetic anhydride at 25 - 30℃; for 48h; regioselective reaction; | 82% |
With dipotassium peroxodisulfate; palladium diacetate; trifluoroacetic acid; trifluoroacetic anhydride at 20℃; regioselective reaction; | 82% |
With dipotassium peroxodisulfate; [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; trifluoroacetic acid; trifluoroacetic anhydride at 80℃; for 20h; Sealed tube; regioselective reaction; | 51% |
2,2',4-Trihydroxybenzophenone
dimethyl sulfate
(2-hydroxy-4-methoxyphenyl)(2-hydroxyphenyl)-methanone
Conditions | Yield |
---|---|
With sulfolane; sodium carbonate; zinc(II) chloride In toluene at 45℃; for 2h; Solvent; | 74.43% |
2-Hydroxy-4-methoxybenzaldehyde
salicylaldehyde
A
bis(2-hydroxy-4-methoxyphenyl)-methanone
B
2,2'-dihydroxybenzophenone
C
(2-hydroxy-4-methoxyphenyl)(2-hydroxyphenyl)-methanone
Conditions | Yield |
---|---|
With dicarbonyl(acetylacotonato)rhodium(I); copper(II) acetate monohydrate; sodium carbonate In N,N-dimethyl-formamide at 100℃; for 16h; Schlenk technique; Inert atmosphere; | A 30% B 41% C 27% |
2,2',4-trimethoxybenzophenone
A
3-hydroxyxanthen-9-one
B
(2-hydroxy-4-methoxyphenyl)(2-hydroxyphenyl)-methanone
Conditions | Yield |
---|---|
With pyridine hydrochloride |
2-Methoxybenzoyl chloride
1,3-Dimethoxybenzene
(2-hydroxy-4-methoxyphenyl)(2-hydroxyphenyl)-methanone
Conditions | Yield |
---|---|
With aluminium trichloride; chlorobenzene |
2-Methoxybenzoyl chloride
(2-hydroxy-4-methoxyphenyl)(2-hydroxyphenyl)-methanone
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 2: pyridine hydrochloride View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 2: pyridine hydrochloride View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: palladium diacetate; dipotassium peroxodisulfate / 4 h / 50 °C 2: silica gel / hexane; dichloromethane View Scheme |
(2-hydroxy-4-methoxyphenyl)(2-hydroxyphenyl)-methanone
Conditions | Yield |
---|---|
With silica gel In hexane; dichloromethane |
(2-hydroxy-4-methoxyphenyl)(2-hydroxyphenyl)-methanone
acetylenemagnesium bromide
Conditions | Yield |
---|---|
In tetrahydrofuran at 0 - 70℃; for 3h; Grignard Reaction; Inert atmosphere; | 80% |
Conditions | Yield |
---|---|
With pyridine hydrochloride at 210 - 215℃; for 6h; | 69% |
mer-[(1,4-bis(diphenylphosphino)butane)aquatrichlororuthenium(III)]
(2-hydroxy-4-methoxyphenyl)(2-hydroxyphenyl)-methanone
Conditions | Yield |
---|---|
Stage #1: (2-hydroxy-4-methoxyphenyl)(2-hydroxyphenyl)-methanone With sodium hydroxide In methanol pH=9; Stage #2: mer-[(1,4-bis(diphenylphosphino)butane)aquatrichlororuthenium(III)] In methanol | 24% |
phenylacetic acid
methyl magnesium iodide
(2-hydroxy-4-methoxyphenyl)(2-hydroxyphenyl)-methanone
(Z,E)-4-(2-hydroxy-4-methoxyphenyl)-4-(2'-hydroxyphenyl)-2-methyl-3-phenylbut-3-en-2-ol
Conditions | Yield |
---|---|
Multistep reaction; |
(2-hydroxy-4-methoxyphenyl)(2-hydroxyphenyl)-methanone
5-<(9-oxoxanthen-3-yl)oxy>valeric acid
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 69 percent / Py*HCl / 6 h / 210 - 215 °C 2: 86 percent / K2CO3 / acetone / 8 h / Heating 3: 1.) NaOH, 2.) HCl / 1.) EtOH, H2O, 25 deg C, 4 h, 2.) H2O, pH 3.5. View Scheme |
(2-hydroxy-4-methoxyphenyl)(2-hydroxyphenyl)-methanone
ethyl 5-<(9-oxoxanthen-3-yl)oxy>valerate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 69 percent / Py*HCl / 6 h / 210 - 215 °C 2: 86 percent / K2CO3 / acetone / 8 h / Heating View Scheme |
(2-hydroxy-4-methoxyphenyl)(2-hydroxyphenyl)-methanone
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: 69 percent / Py*HCl / 6 h / 210 - 215 °C 2: 86 percent / K2CO3 / acetone / 8 h / Heating 3: 1.) NaOH, 2.) HCl / 1.) EtOH, H2O, 25 deg C, 4 h, 2.) H2O, pH 3.5. 4: 1.) NaBH4, NaOH, 2.) NaHCO3 / 1.) H2O, 50-55 deg C, 3 h, pH 8.0-8.5, 2.) 10 deg C, 1 h. View Scheme |
(2-hydroxy-4-methoxyphenyl)(2-hydroxyphenyl)-methanone
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: 69 percent / Py*HCl / 6 h / 210 - 215 °C 2: 86 percent / K2CO3 / acetone / 8 h / Heating 3: 1.) NaOH, 2.) HCl / 1.) EtOH, H2O, 25 deg C, 4 h, 2.) H2O, pH 3.5. 4: 1.) NaOH, Zn, 2.) TFA / 1.) aq. EtOH, reflux, 6 h, 2.) 1,2-dimethoxyethane, 25 deg C, 4 h. View Scheme |
Conditions | Yield |
---|---|
With potassium iodide; potassium carbonate In water; ethyl acetate; isopropyl alcohol |
(2-hydroxy-4-methoxyphenyl)(2-hydroxyphenyl)-methanone
2,2',4-Trihydroxybenzophenone
Conditions | Yield |
---|---|
With boron tribromide In dichloromethane at -78 - 20℃; | |
With boron tribromide In dichloromethane for 48h; Inert atmosphere; |
Conditions | Yield |
---|---|
In dimethyl sulfoxide at 20℃; for 12h; |
(2-hydroxy-4-methoxyphenyl)(2-hydroxyphenyl)-methanone
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: tetrahydrofuran / 3 h / 0 - 70 °C / Inert atmosphere 2: N-ethyl-N,N-diisopropylamine; (5aR,10bS)-2-mesityl-5a,10b-dihydro-4H,6H-indeno[2,1-b][1,2,4]triazolo[4,3-d][1,4]oxazin-2-ium tetrafluoroborate / dichloromethane / 36 h / 24 °C / Molecular sieve; Inert atmosphere View Scheme |
(2-hydroxy-4-methoxyphenyl)(2-hydroxyphenyl)-methanone
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: tetrahydrofuran / 3 h / 0 - 70 °C / Inert atmosphere 2: N-ethyl-N,N-diisopropylamine; BF4(1-)*C21H22N3O(1+) / dichloromethane / 36 h / 24 °C / Molecular sieve; Inert atmosphere View Scheme |
(2-hydroxy-4-methoxyphenyl)(2-hydroxyphenyl)-methanone
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: potassium iodide; potassium carbonate / water; ethyl acetate; isopropyl alcohol 2: methanol; hexane 3: hydrogen; acetic acid / palladium / ethanol; hexane; water; ethyl acetate View Scheme |
(2-hydroxy-4-methoxyphenyl)(2-hydroxyphenyl)-methanone
3-Methoxy-12H-dibenzo-[d,g][1,3]dioxocin-6-carboxylic Acid
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: potassium iodide; potassium carbonate / water; ethyl acetate; isopropyl alcohol 2: methanol; hexane 3: hydrogen; acetic acid / palladium / ethanol; hexane; water; ethyl acetate 4: sodium hydroxide / tetrahydrofuran; water View Scheme |
(2-hydroxy-4-methoxyphenyl)(2-hydroxyphenyl)-methanone
Methyl 3-Methoxy-12H-dibenzo[d,g][1,3]dioxocin-12-one-6-carboxylate
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: potassium iodide; potassium carbonate / water; ethyl acetate; isopropyl alcohol 2: methanol; hexane View Scheme |
(2-hydroxy-4-methoxyphenyl)(2-hydroxyphenyl)-methanone
A
2,2',4-Trihydroxybenzophenone
B
(2,4-dihydroxyphenyl)(2-hydroxy-4-methoxyphenyl)methanone
Conditions | Yield |
---|---|
With water; NADPH In aq. phosphate buffer at 37℃; for 2.5h; pH=7.4; Microbiological reaction; |
The IUPAC name of Dioxybenzone is (2-hydroxy-4-methoxyphenyl)-(2-hydroxyphenyl)methanone. With the CAS registry number 131-53-3, it is also named as Benzophenone-8; 2,2'-Dihydroxy-4-methoxybenzophenone; Methanone, (2-hydroxy-4-methoxyphenyl)(2-hydroxyphenyl)-; Cyasorb UV 24 Light Absorber; Spectra-sorb UV 24; Advastab 47. The product's categories are industrial/fine chemicals, aromatic benzophenones & derivatives (substituted), benzophenones (for high-performance polymer research), functional materials, reagent for high-performance polymer research and ketone.
The Dioxybenzone is yellow powder which is insoluble in water, but moderately soluble in ethanol and isopropanol. It is stable and incompatible with strong oxidizing agents. This product is UV absorbers, and applied to PVC, ABS resin, acrylic resin, polyurethane, melamine resin, cellulose resin, and many other plastics. This chemical can be obtained by the following method. By the condensation of resorcinol and salicylaldehyde chloride, and then methylation of dimethyl sulfate .
This product is probably combustible. When heated to decomposition it emits acrid smoke and irritating vapors. It is irritating to eyes, respiratory system and skin. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. If you want to contact this product, you must wear suitable protective clothing.
The other characteristics of this product can be summarized as: (1)ACD/LogP: 3.93 ; (2)# of Rule of 5 Violations: 0 ; (3)ACD/LogD (pH 5.5): 3.92 ; (4)ACD/LogD (pH 7.4): 3.31 ; (5)ACD/BCF (pH 5.5): 554.77 ; (6)ACD/BCF (pH 7.4): 135.6 ; (7)ACD/KOC (pH 5.5): 3176.36 ; (8)ACD/KOC (pH 7.4): 776.39 ; (9)#H bond acceptors: 4 ; (10)#H bond donors: 2 ; (11)#Freely Rotating Bonds: 5 ; (12)Index of Refraction: 1.623 ; (13)Molar Refractivity: 66.48 cm3 ; (14)Molar Volume: 188.4 cm3 ; (15)Polarizability: 26.35×10-24 cm3 ; (16)Surface Tension: 55.2 dyne/cm ; (17)Enthalpy of Vaporization: 64.68 kJ/mol ; (18)Vapour Pressure: 3.73E-06 mmHg at 25°C ; (19)Rotatable Bond Count: 3 ; (20)Tautomer Count: 24 ; (21)Exact Mass: 244.073559 ; (22)MonoIsotopic Mass: 244.073559 ; (23)Topological Polar Surface Area: 66.8 ; (24)Heavy Atom Count: 18.
People can use the following data to convert to the molecule structure. SMILES: O=C(c1ccc(OC)cc1O)c2ccccc2O; InChI: InChI=1/C14H12O4/c1-18-9-6-7-11(13(16)8-9)14(17)10-4-2-3-5-12(10)15/h2-8,15-16H,1H3. Dioxybenzone has many suppliers, such as Changzhou Sunlight Pharmaceutical Co., Ltd..
The following is the toxicity data which has been tested.
1. | mmo-sat 12,500 µg/L | ENMUDM Environmental Mutagenesis. 4 (1982),340. | ||
2. | mma-sat 3 µg/plate | ENMUDM Environmental Mutagenesis. 8 (Suppl 7)(1986),1. | ||
3. | mma-mus:lyms 32 µg/plate | JACTDZ Journal of the American College of Toxicology. 2 (5)(1983),35. |
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