Chemical Name: Benzophenone ; Chinese Supplier CAS No.: 119-61-9 Molecular Formula: C13H10O Properties: White to whitish crystal, with light odor. Soluble in alcohol, ether ,and chloroform; insoluble in water. Specification: (Q/CFH07-2001)
Cas:119-61-9
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inquiryAppearance:White crystal flake Storage:R.T Package:25kg/Bag Application:Photoinitiators of UV products, pharmaceutical intermediates, fragrances, light stabilizers, etc. Transportation:Express/Sea/Air Port:Any port in China
Cas:119-61-9
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inquiryPhysical property: White crystal powder with slight rose fragrance; Melting point:48.5°C Boiling point:305.4°C Our advantage: 1. 24hours to reply your E-mail; 2. Customized pakage; 3. Adequate stocks; 4. The competitive price
Cas:119-61-9
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inquirySpecifications CAS No.: 119-61-9 Other Names: Diphenyl ketone; Diphenylmethanone MF: C13H10O EINECS No.: 204-337-6 Place of Origin: China (Mainland) Type: Syntheses Material Intermediates Purity: 98% Brand Name: Luyunjia Model Number
Cas:119-61-9
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inquiryGeneral Chemacure PI-BP is a highly effective Type II photoinitiator, used in combination with tertiary amine synergists for UV-polymerisation of suitable resins. Applications □ Overprint Varnish □
Chongqing Changfeng Chemical Co., Ltd. is the world’s largest manufacturer of Benzophenone with an annual capacity of 4000 mt, and utilizes the chemically- efficient and environmentally-friendly phosgene manufacturing process. Appearanc
Benzophenone CAS:119-61-9 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organic intermediates,
Cas:119-61-9
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inquiryShanghai Lonwin Chemical company is a subsidiary of Lonwin Industry Group Limited, was established in 2011 and is headquartered in Shanghai, adjacent to China National Convention and Exhibition Center and Hongqiao transportation hub. Lonwinchem i
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inquiryHRcure-BP manufacturer CAS 119-61-9 High cost performance UV absorption Peak:251nm, 333nm Tianjin Huiren chemtech Co. , Ltd. , established in January 2016, is a national high-tech enterprise that integrates R&D, production and mark
Cas:119-61-9
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inquiryDayangchem's R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. DayangChem can provide different quantities
Cas:119-61-9
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inquiryItems Standard Result Appearance White Flakes White Flakes Purity 99.7% min
Cas:119-61-9
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inquiryWelcome to Simagchem, your partner in China as a premier supply of bulk specialty chemicals for industry and life science. We introduce experienced quality product and exceptional JIT service with instant market intelligence in China to benefit our
Cas:119-61-9
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inquirySpecifications CAS No.: 119-61-9 Other Names: Crystal Benzophenone MF: C13H10O EINECS No.: 204-337-6 Place of Origin: Shanghai, Chin
Cas:119-61-9
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Type:Other
inquiryProduct description: Product name Benzophenone CAS number 119-61-9 Assay ≥99.5% Appearance White flake crsytal Capacity 1000mt/year Application Photoinitiator/pharmaceutical/
Cas:119-61-9
Min.Order:100 Gram
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inquiryUnique advantages for Benzophenone Cas 119-61-9 Guaranteed purity High quality & competitive price Quality control Fast feedback Prompt shipment Appearance:White or off-white crystalline powder Storage:Refrigerator Package:25kg/drum
Cas:119-61-9
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inquiryHebei yanxi chemical co. LTD. has expanded a compositive entity from initially only as a small manufacturer. The company dedicated to the development, production and marketing of chemicals. After many years of efforts, we have established stable
Buy Benzophenone 99.5% CAS No: 119-61-9, a chemical intermediate for industry, cosmetic and pharmaceuticals uses from TNJ Chemical, China leading Benzophenone 99.5% suppliers, factory & manufacturers. If you want to buy Benzophenone 99.5% Appea
Cas:119-61-9
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The above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
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Cas:119-61-9
Min.Order:1 Gram
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inquiryBenzophenone Manufacturer Factory CAS 119-61-9 Benzophenone Manufacturer High quality Best price In stock factory CAS 119-61-9 Benzophenone COA TDS price MSDS highly quality and immedaite delivery Name Benzophenone Synonyms
Cas:119-61-9
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inquiryOur company was built in 2009 with an ISO certificate.In the past 5 years, we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so on.O
Cas:119-61-9
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inquiryOur advantages: 1. High quality and competitive price: 1) Standard: BP/USP/EP/ enterprise standard 2) All purity 鈮 9% 3) We are manufacturers and can provide high quality products at factory prices. 2. Fast and safe delivery 1) The package can
Cas:119-61-9
Min.Order:1 Metric Ton
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inquiryWITH US,YOUR MONEY IN SAFE,YOUR BUSINESS IN SAFE 1)Quick Response Within 12 hours; 2)Quality Guarantee: All products are strictly tested by our QC, confirmed by QA and approved by third party lab in China, USA, Canada, Germany, UK, Italy, France et
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inquiryProduct name Benzophenone CAS NO. 119-61-9 Color White Appearance Powder Appearance: White powder Storage:Store in cool and dry plac
We are leading fine chemicals supplier in China and Our main business covers the fields below: 1.Noble Metal Catalysts (Pt.Pd...) 2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...) 3.OLED intermediat
Cas:119-61-9
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Hanways chempharm is a specialized company concentrating on the R&D, production, marketing and technical service of APIs and pharmaceutical intermediates. The marketing department is located in Wuhan. We have two GMP facilities in Hubei Pr
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Cas:119-61-9
Min.Order:1 Kilogram
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inquiryWe are the manufacturers and suppliers of API in China, and warehouse in Germany and USA of California, which can quickly and safely deliver to your address 1.High quality and competitive price. 2.Free sample for your evaluation. 3.Promptly delivery
Cas:119-61-9
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inquiryConditions | Yield |
---|---|
Stage #1: 1,1-Diphenylethylene for 0.05h; Inert atmosphere; Stage #2: With tert.-butylhydroperoxide at 102℃; for 24h; Inert atmosphere; | 100% |
With oxygen at 110℃; for 8h; Temperature; Schlenk technique; | 99% |
With oxygen at 110℃; for 8h; Temperature; Sealed tube; | 99% |
Conditions | Yield |
---|---|
With acetone; zirconic acid In benzene at 80℃; for 8h; | 100% |
With bis(2,2'-bipyridyl) copper(II) permanganate In dichloromethane for 0.5h; Ambient temperature; | 100% |
With tert.-butylhydroperoxide; polystyrene-bound phenylselenic acid In tetrachloromethane for 24h; Heating; | 100% |
Conditions | Yield |
---|---|
With potassium permanganate; iron(III) chloride In acetone at -78 - 20℃; for 16h; | 100% |
With chromyl chloride In dichloromethane at 22℃; for 0.5h; ultrasound sonication; | 99% |
With tert.-butylhydroperoxide; C45H52CuN4O3 In decane; acetonitrile at 70℃; for 18h; | 99% |
Conditions | Yield |
---|---|
With pyridine chromium peroxide In dichloromethane for 0.3h; Product distribution; Ambient temperature; effect of various chromium(VI) based oxidants; | 100% |
In acetic acid for 0.25h; Heating; | 100% |
With sodium hydroxide; copper(III) periodate for 0.05h; Heating; oxidative decarboxylation of α-hydroxy acids; var. α-hydroxy acids, also Cu(III) tellurate as oxidant; | 95% |
methanol
2,2-Dimethyl-4,4-diphenyl-3,3-bis(trimethylsilyl)-1-oxa-2-silacyclobutan
A
benzophenone
B
1-(Dimethylmethoxysilyl)-1,1-bis(trimethylsilyl)ethan
Conditions | Yield |
---|---|
In benzene at 110℃; for 40h; Rate constant; half live time; | A n/a B 100% |
Conditions | Yield |
---|---|
Stage #1: Benzophenone imine With chloro-trimethyl-silane; sodium iodide In acetonitrile at 20℃; Stage #2: With water In acetonitrile for 0.0833333h; | 100% |
With hydrogenchloride; water at 40℃; | 86% |
With water at 25℃; Rate constant; effect of pH on the rate constants; |
2,2-diphenyl-1,3-benzodithiole
benzophenone
Conditions | Yield |
---|---|
With tetrafluoroboric acid; mercury(II) oxide In tetrahydrofuran for 0.166667h; Ambient temperature; | 100% |
2,2-diphenyl-1,3-oxathiolane
benzophenone
Conditions | Yield |
---|---|
With 2,2,2-trifluoroethanol; oxygen; vanadium(V) oxychloride for 5h; deprotection; Heating; | 100% |
Stage #1: 2,2-diphenyl-1,3-oxathiolane In ethanol at 20℃; Stage #2: With water In ethanol at 20℃; | 98% |
With silver(I) nitrite; iodine In tetrahydrofuran for 0.5h; Mechanism; Ambient temperature; other mono- and dithioacetals; | 96% |
Conditions | Yield |
---|---|
With K-10 clay supported iron(III) nitrate nonahydrate In dichloromethane for 3h; Ambient temperature; with K-10 clay-supported copper(II) nitrate trihydrate; | 100% |
With trichloroisocyanuric acid; silver nitrate In water; acetonitrile Ambient temperature; | 100% |
With hydrogenchloride; sodium nitrate In tetrachloromethane; water for 1h; Ambient temperature; other reagent; | 100% |
diphenylmethyl trimethylsilyl ether
benzophenone
Conditions | Yield |
---|---|
With 2,6-dicarboxypyridinium fluorochromate In acetonitrile at 20℃; for 0.0833333h; Reflux; | 100% |
With nitrogen dioxide at 20℃; for 0.5h; | 100% |
With chromium(VI) oxide; tert.-butylhydroperoxide; triphenylhydroxysilane In dichloromethane for 24h; Ambient temperature; | 99% |
2,2-diphenyl-1,3-dithiane
benzophenone
Conditions | Yield |
---|---|
With tetrafluoroboric acid; mercury(II) oxide In tetrahydrofuran Ambient temperature; | 100% |
With dihydrogen peroxide; iodine; sodium dodecyl-sulfate In water at 20℃; for 0.333333h; Micellar solution; | 100% |
With 2,4,4,6-Tetrabromo-2,5-cyclohexadien-1-one; dihydrogen peroxide In water; acetonitrile at 20℃; for 0.75h; | 100% |
Conditions | Yield |
---|---|
With water; Nafion-H In acetone for 0.5h; | 100% |
With water; 2,3-dicyano-5,6-dichloro-p-benzoquinone In acetonitrile for 1h; Ambient temperature; | 100% |
sodium tetrakis[(3,5-di-trifluoromethyl)phenyl]borate In water at 30℃; for 0.5h; | 99% |
Conditions | Yield |
---|---|
With N-Bromosuccinimide; triphenylbismuthane; potassium carbonate In water; acetonitrile for 2h; Ambient temperature; | 100% |
With naphthalene-1,4-dicarbonitrile; oxygen for 90h; Irradiation; | 100% |
With dinitrogen tetraoxide; ferric nitrate In ethyl acetate Heating; further oxidizing agent; | 100% |
Conditions | Yield |
---|---|
With hydrogenchloride; sodium nitrate In tetrachloromethane; water for 1h; Ambient temperature; other reagent; | A n/a B 100% |
2-diphenylmethyliumyl-3,5-dioxo-4-phenyl-1,2,4-triazolidin-1-ide
A
benzophenone
B
4-Phenylurazole
Conditions | Yield |
---|---|
With water for 1080h; | A 100% B 100% |
With atmospheric moisture storage conditions; |
(1R,5S)-4-Methyl-1,3,5,7,7-pentaphenyl-6-oxa-2,4-diaza-bicyclo[3.2.0]hept-2-ene
A
benzophenone
B
1-methyl-2,4,5-triphenyl-1H-imidazole
Conditions | Yield |
---|---|
In various solvent(s) at 120℃; for 2.5h; Thermodynamic data; cycloreversion of further oxetane derivatives; | A 100% B 100% |
Conditions | Yield |
---|---|
In various solvent(s) -78 deg C, 0.5 h, 0 deg C, 0.5 h; | 100% |
acetic acid
4,4a-dihydro-3,3-dimethyl-1-phenyl-4,4-bis(trimethylsilyl)-3H-2-oxa-3-silanaphthaline
A
benzophenone
Conditions | Yield |
---|---|
In benzene at 90℃; for 3h; Rate constant; half live time; | A n/a B 100% |
2-diphenylmethylene-1,3-benzodithiole 1,1,3,3-tetraoxide
A
benzophenone
B
2H-benzo[d][1,3]dithiole 1,1,3,3-tetraoxide
Conditions | Yield |
---|---|
With potassium hydroxide In 1,4-dioxane for 0.5h; Product distribution; Heating; further educt: 2-diphenylmethylene-1,3-benzodithiole 1,1-dioxide; | A 100% B 88% |
With potassium hydroxide In 1,4-dioxane for 0.5h; Heating; Yields of byproduct given; | A n/a B 88% |
4,4a-dihydro-3,3-dimethyl-1-phenyl-4,4-bis(trimethylsilyl)-3H-2-oxa-3-silanaphthaline
tert-butyl alcohol
A
benzophenone
B
tert-Butoxydimethylsilyl-bis(trimethylsilyl)methan
Conditions | Yield |
---|---|
In benzene at 90℃; for 1.5h; Rate constant; half live time; | A n/a B 100% |
Conditions | Yield |
---|---|
With 1,2-bis(diphenylphosphino)ethane nickel(II) chloride In tetrahydrofuran at 0℃; | 100% |
Stage #1: benzoyl chloride With 1-methyl-pyrrolidin-2-one In toluene at 0℃; for 0.5h; Stage #2: phenylmagnesium bromide In tetrahydrofuran; toluene at -10 - 0℃; for 4.25h; chemoselective reaction; | 89% |
In 2-methyltetrahydrofuran at 25℃; for 1h; Solvent; Concentration; Flow reactor; Green chemistry; | 85% |
Conditions | Yield |
---|---|
With 2-phenyl-1,2-benzoisoselenazol-3(2H)-one; dihydrogen peroxide In methanol; water at 65℃; for 72h; | 100% |
With ammonium cerium(IV) nitrate In water; acetonitrile at 50℃; for 16h; Oxidation; | 90% |
With potassium permanganate; montmorillonite K-10 for 0.5h; | 90% |
With 3-carboxypyridinium chlorochromate In acetonitrile for 3h; Heating; | 87% |
Conditions | Yield |
---|---|
With oxygen; methylene blue In benzene at 20℃; for 0.5h; Mechanism; Irradiation; N2/N2O ratio; var. solvent; other diazomethanes; | A 100% B n/a |
benzophenone
Conditions | Yield |
---|---|
With tris paraperiodate In benzene for 1h; Heating; | 100% |
2-Fluorobenzoyl chloride
1,4-dimethoxybezene
A
benzophenone
B
2-methoxy-9H-xanthen-9-one
Conditions | Yield |
---|---|
With hydrogenchloride In AlCl3; 1,2-dichloro-ethane | A n/a B 100% |
Conditions | Yield |
---|---|
With sodium chlorite; sodium dihydrogenphosphate In tetrahydrofuran; water; tert-butyl alcohol diastereoselective reaction; | A 100% B 35% |
benzophenone
Conditions | Yield |
---|---|
With oxygen In benzene for 0.75h; | 100% |
1,1-Diphenylmethanol
diisopropyl-carbodiimide
A
benzophenone
B
N1,N2-Diisopropylformamidine
Conditions | Yield |
---|---|
With ruthenium complex In toluene at 120℃; for 24h; Inert atmosphere; Sealed tube; | A 100% B 74 %Spectr. |
Conditions | Yield |
---|---|
With K-10 clay supported copper(II) nitrate trihydrate In dichloromethane for 4h; Ambient temperature; with K-10 clay-supported iron(III) nitrate nonahydrate; | 99.5% |
With K-10 clay supported copper(II) nitrate trihydrate In dichloromethane for 4h; Ambient temperature; K-10 clay supported iron(III) nitrate nonahydrate; | 99.5% |
With dihydrogen peroxide; vanadia; ammonium bromide In dichloromethane; water at 0 - 5℃; for 2h; | 95% |
Conditions | Yield |
---|---|
With sodium hydroxide; N-benzyl-N,N,N-triethylammonium chloride In toluene for 3h; | 99% |
With tetrabutylammomium bromide; oxygen In N,N-dimethyl-formamide Hg cathode, Pt anode, -1.0 V vs SCE; | 95% |
With oxygen; potassium carbonate In water; dimethyl sulfoxide Ambient temperature; | 95% |
ethyl 2-bromoisobutyrate
benzophenone
Ethyl 3-hydroxy-2,2-dimethyl-3,3-diphenylpropanoate
Conditions | Yield |
---|---|
With iodine; zinc In 1,4-dioxane for 0.166667h; Reformatsky reaction; ultrasound irradiation; | 100% |
With magnesium; benzene | |
With zinc; benzene | |
With zinc |
Conditions | Yield |
---|---|
With Et2OFe(catecholate-porous organic polymer) In benzene-d6 at 23℃; for 0.0833333h; | 100% |
Conditions | Yield |
---|---|
With zinc(II) tetrahydroborate In acetonitrile for 16h; Mechanism; Ambient temperature; | 100% |
With zinc(II) tetrahydroborate In acetonitrile for 16h; Ambient temperature; | 100% |
With samarium; 1,2-Diiodoethane In 1,2-dimethoxyethane for 24h; Ambient temperature; | 100% |
Conditions | Yield |
---|---|
With trifluorormethanesulfonic acid; 3-chloro-benzenecarboperoxoic acid In dichloromethane for 6h; Ambient temperature; | 100% |
With hydrogenchloride In chloroform at 20℃; for 8h; Baeyer-Villiger oxidation; | 100% |
With dihydrogen peroxide; iodine; acetic acid at 20℃; for 0.166667h; Baeyer-Villiger oxidation; | 93% |
Conditions | Yield |
---|---|
With hydroxylamine hydrochloride; sodium acetate In methanol Heating; | 100% |
With hydroxylamine hydrochloride; sodium acetate In methanol; water Reflux; | 100% |
With hydroxylamine hydrochloride In ethanol at 50 - 60℃; for 1.5h; | 100% |
Conditions | Yield |
---|---|
With hydrogen; aluminum oxide; K5PV2Mo10O40 at 300℃; under 17480 Torr; for 3.33333h; Catalytic hydrogenation; | 100% |
With iodine; hypophosphorous acid In acetic acid for 24h; Reduction; Heating; | 100% |
With hydrogen In methanol at 20℃; under 760.051 Torr; for 10h; chemoselective reaction; | 100% |
Conditions | Yield |
---|---|
With hydrazine hydrate In ethanol for 12h; Heating; | 100% |
With hydrazine hydrate; acetic acid In ethanol at 100℃; for 21h; Inert atmosphere; | 100% |
With hydrazine hydrate In ethanol for 4h; Reflux; | 100% |
Conditions | Yield |
---|---|
With woollins’ reagent In toluene for 20h; Heating; | 100% |
With titanium tetrachloride; zinc In tetrahydrofuran at 0 - 70℃; for 12h; Inert atmosphere; | 98% |
With pyridine; titanium tetrachloride; zinc In 1,4-dioxane for 0.0833333h; microwave irradiation; | 97% |
Conditions | Yield |
---|---|
With hydrogen sulfide; phosphorous acid trimethyl ester In diethylene glycol dimethyl ether for 2.75h; Product distribution; Irradiation; variation of solvents, reagents and conditions; | 100% |
With hydrogen sulfide; phosphorous acid trimethyl ester In diethylene glycol dimethyl ether for 2.75h; Irradiation; | 100% |
With iodine; magnesium In diethyl ether; benzene for 0.5h; pinacol coupling; sonication; | 99% |
Conditions | Yield |
---|---|
Nafion-H In benzene Heating; | 100% |
With cobalt(II) bromide In dichloromethane for 4h; Ambient temperature; | 99% |
With amberlyst-15 In acetonitrile for 1h; | 99.91% |
Conditions | Yield |
---|---|
With ammonium acetate; zinc In tetrahydrofuran at 0℃; for 0.0166667h; Barbier reaction; | 100% |
With manganese; chloro-trimethyl-silane; indium In tetrahydrofuran at 20℃; for 4h; Alkylation; | 98% |
With manganese; chloro-trimethyl-silane; indium In tetrahydrofuran at 20℃; for 4h; Barbier allylation; | 98% |
Conditions | Yield |
---|---|
With zinc In tetrahydrofuran for 0.5h; | 100% |
Stage #1: propargyl bromide With n-butyllithium; N,N,N,N,-tetramethylethylenediamine In diethyl ether; hexane at -78℃; for 0.333333h; Stage #2: benzophenone In diethyl ether at -78 - 20℃; for 2h; Stage #3: With hydrogen cation In diethyl ether | 96% |
Stage #1: benzophenone; propargyl bromide With dysprosium; sodium iodide; mercury dichloride In tetrahydrofuran at -14 - 20℃; Propargylation; Stage #2: With hydrogenchloride In water Hydrolysis; | 92% |
Conditions | Yield |
---|---|
With t-Bu-P4 base In toluene at -78℃; for 1h; | 100% |
Stage #1: 1,3-Benzothiazole; benzophenone With tetrakis{[tris(dimethylamino)phosphoranyliden]amino}phosphonium fluoride; tris(trimethylsilyl)amine In toluene at 25℃; for 24h; Inert atmosphere; Stage #2: In tetrahydrofuran Reagent/catalyst; | 94% |
With n-butyllithium In tetrahydrofuran; hexane -78 deg C, 1 h; 10 min; | 88% |
benzophenone
3-methoxyphenyl bromide
(3-methoxyphenyl)(diphenyl)methanol
Conditions | Yield |
---|---|
Stage #1: 3-methoxyphenyl bromide With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 0.5h; Inert atmosphere; Stage #2: benzophenone In tetrahydrofuran; hexane at -78 - 20℃; Inert atmosphere; | 100% |
With magnesium 1.) ether, 2.) a) RT, 6 h, b) reflux, 1 h; Yield given. Multistep reaction; | |
With n-butyllithium |
benzophenone
(Z)-ethyl cinnamate
(Z)-4-Hydroxy-3,4,4-triphenyl-but-2-enoic acid ethyl ester
Conditions | Yield |
---|---|
With 2,2,6,6-tetramethyl-piperidine In tetrahydrofuran at -100℃; for 1.25h; Product distribution; other solvents, amount of reagents and different reaction times; | 100% |
With 2,2,6,6-tetramethyl-piperidine In tetrahydrofuran at -100℃; for 1.25h; | 100% |
benzophenone
trimethyl(2-methylenebut-3-enyl)silane
3-methylene-5,5-diphenyl-5-(trimethylsiloxy)pentene
Conditions | Yield |
---|---|
With tetrabutyl ammonium fluoride In tetrahydrofuran at 50℃; for 2.5h; | 100% |
With tetrabutyl ammonium fluoride In tetrahydrofuran at 50℃; for 2.5h; | 100% |
Conditions | Yield |
---|---|
Stage #1: Methyltriphenylphosphonium bromide With n-butyllithium In tetrahydrofuran Stage #2: benzophenone In tetrahydrofuran at 20℃; for 6h; Wittig reaction; | 100% |
Stage #1: Methyltriphenylphosphonium bromide With n-butyllithium In tetrahydrofuran at 0℃; for 1h; Inert atmosphere; Stage #2: benzophenone In tetrahydrofuran at 20℃; Inert atmosphere; | 94% |
Stage #1: Methyltriphenylphosphonium bromide With potassium tert-butylate In diethyl ether at 20℃; for 0.25h; Inert atmosphere; Stage #2: benzophenone In diethyl ether at 0℃; for 15h; Inert atmosphere; | 87% |
benzophenone
(dichloroalumino)(trichlorotitanio)methane
1,1-Diphenylethylene
Conditions | Yield |
---|---|
In toluene for 0.5h; Heating; | 100% |
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