As a leading manufacturer and supplier of chemicals in China, DayangChem not only supply popular chemicals, but also DayangChem's R&D center offer custom synthesis services. DayangChem can provide different quantities of custom synthesis ch
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inquiryProduct Description Product Name Tropolone CAS No. 533-75-5 Appearance Off-white to yellowish crystal Assay ≥99% Capacity 100mt/year Min.packing 100gram
he company has advanced technology, as well as a large number of excellent R & D team, to provide customers from the grams to one hundred kilograms and tons of high-quality products, competitive prices and quality se T rvice Appearance:white po
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inquiry1. Factory price and high quality must be guaranteed, base on 8 years of production and R&D experience2. Free samples will be provided,ensure specifications and quality are right for customer3. Customers will receive the most professional technical s
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inquiryhebei yanxi chemical co., LTD who registered capital of 10 million yuan, nearly to $2 million, we have a pharmaceutical raw materials factory production of pharmaceutical raw materials, and a reagent r&d center, and we do research and developm
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inquiryOur main production base is located in Xuzhou industry park. We are certified both to the ISO 9001 and ISO 14001 Standards, have a safety management system in place.Our R&D team masters core technology for process-design of target building block
Welcome to Henan Tianfu Chemical Co., Ltd. website. Our company engages in Sodium Tripolyphosphate (STPP) and Sodium Hexametabphosphate (SHMP) production; development of noble metal catalysts, synthesis of electronic chemical materials and general
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inquiryOur advantages: 1. All inquiries will be replied within 12 hours. 2. Dedication to quality, supply & service. 3. Strictly on selecting raw materials. 4. Reasonable & competitive price, fast lead time. 5. Sample is available for your eva
WITH 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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inquirySymonyms 2-Hydroxy-2,4,6-cycloheptatrien-1-one CAS No. 533-75-5 Appearance Light yellow or yellow crys
1.No Less 8 years exporting experience. Clients can 100% received goods 2.Lower Price with higher quality 3,Free sample 4,We are sincerely responsible for the "product quality" and "After Service" Upbio is Specialized
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inquiryTropolone CAS:533-75-5 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, s
Cas:533-75-5
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inquiryHello, dear friend! I'm Hansen and Allen from China. Welcome to my lookchem mall! The following is a brief introduction of our company's products and services. If you are interested in our products, please contact us by emai
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inquiryPRODUCT DETAILS Tropolone Basic information
Cas:533-75-5
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inquiryHenan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
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inquiryOur advantage: high quality with competitive price High quality standard: BP/USP/EP Enterprise standard All purity customized Fast and safe delivery We have reliable forwarder who can help us deliver our goods more fast and safe. We have s
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inquiry1. Timely and efficient service to ensure communication with customers 2. Produce products of different specifications and sizes according to your requirements. 3. Quality procedures and standards recognized by SGS. Advanced plant equipment ensures
Hangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
J&H CHEM 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. J&H CHEM has some Manufacturing base in Jia
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Zibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi
Cas:533-75-5
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inquiryProduct name: Tropolone CAS No.:533-75-5 Molecule Formula:C7H6O2 Molecule Weight:122.12 Purity: 99% Package: 25kg/drum Description:Light yellow crystalline powder Manufacture Standards:Enterprise Standard TESTING ITEMS
Cas:533-75-5
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inquiryOur Advantages A. International Top level TechnologyOur company owned biomedicine experts are famous at home and abroad with rich experience in research and development in the field of efficient chiral functional molecules research and development an
Tropolone Chemical Properties Melting point 50-52 °C (lit.) Boiling point 80-84 °C/0.1 mmHg (lit.) density 1.1483 (rough estimate) refractive index 1.5286 (estimate) Fp >230 °F storage temp. 2-8°C solubility
factory?direct?saleAppearance:White Powder Storage:Store In Dry, Cool And Ventilated Place Package:25kg/drum, also according to the clients requirement Application:It is widely used as a thickener, emulsifier and stabilizer Transportation:By Sea Or B
Cas:533-75-5
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inquiryHangzhou Huarong Pharm Co., Ltd.established since 2006 , has been actively developing specialty products for Finished Dosages, APIs, Intermediates, and Fine chemicals markets in North America, Europe, Korea, Japan, Mid-East and all over the World. Hu
Shandong Mopai Biotechnology Co., LTD is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemicals. W
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inquiry1.Applied in food field.it can improve the immune system and prolong life. 2.Appliedin cosmetic field.it can improve the skin care. 3.Applied in pharmaceutical field.it can treat various dieases. 4.Our product quality assurance will make our customer
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inquiry2-<(-3-methyl-2-butenyl)oxy>tropone
2-hydroxy-2,4,6-cycloheptatrien-1-one
Conditions | Yield |
---|---|
In dimethyl sulfoxide at 180℃; for 0.5h; | 96% |
2-(cycloheptyloxy)tropone
A
Cycloheptene
B
2-hydroxy-2,4,6-cycloheptatrien-1-one
Conditions | Yield |
---|---|
In dimethylsulfoxide-d6 at 180℃; for 2h; | A 95% B n/a |
In decalin at 180℃; for 2h; |
2-(cyclooctyloxy)tropone
A
(Z)-Cyclooctene
B
2-hydroxy-2,4,6-cycloheptatrien-1-one
Conditions | Yield |
---|---|
In dimethylsulfoxide-d6 at 180℃; for 2h; | A 95% B n/a |
In decalin at 180℃; for 2h; | |
In dimethylsulfoxide-d6 at 180℃; Rate constant; Product distribution; Thermodynamic data; Ea, ΔS(excit.); |
2-(cyclododecyloxy)tropone
A
2-hydroxy-2,4,6-cycloheptatrien-1-one
B
cyclododecene
Conditions | Yield |
---|---|
In dimethylsulfoxide-d6 at 180℃; for 2h; | A n/a B 95% |
(+/-)-7,7-dichlorobicyclo[3.2.0]hept-2-en-6-one
2-hydroxy-2,4,6-cycloheptatrien-1-one
Conditions | Yield |
---|---|
With acetic acid; sodium hydroxide | 95% |
With sodium hydroxide; acetic acid at 130℃; for 7h; Rearrangement; | 87% |
With hydrogenchloride; sodium hydroxide; acetic acid for 8h; pH=1; Heating; | 77% |
With sodium hydroxide; acetic acid for 8h; Heating; | 77% |
2-benzyloxycyclohepta-2,4,6-trienone
A
dimethylsulfide
B
2-hydroxy-2,4,6-cycloheptatrien-1-one
C
benzaldehyde
Conditions | Yield |
---|---|
With dimethyl sulfoxide at 180℃; for 2h; other troponyl ethers; | A n/a B n/a C 82% |
2-hydroxy-2,4,6-cycloheptatrien-1-one
Conditions | Yield |
---|---|
With trimethylsilyl trifluoromethanesulfonate; triethylamine Elimination; | 75% |
2-(cyclopentyloxy)tropone
A
2-hydroxy-2,4,6-cycloheptatrien-1-one
B
cyclopentene
Conditions | Yield |
---|---|
In dimethylsulfoxide-d6 at 180℃; for 2h; | A n/a B 70% |
In dimethyl sulfoxide at 180℃; for 8h; |
2-(p-tolylmethoxy)tropone
A
2-hydroxy-2,4,6-cycloheptatrien-1-one
B
5-(p-tolylmethyl)tropolone
C
3-(p-tolylmethyl)tropolone
Conditions | Yield |
---|---|
In decalin at 190℃; for 11h; | A 10% B 6.6% C 60% |
With dibenzoyl peroxide In decalin at 180.6℃; Rate constant; variation of the amounts of reagent and the time; |
2-(4-chlorophenylmethoxy)tropone
A
2-hydroxy-2,4,6-cycloheptatrien-1-one
B
5-(4-Chloro-benzyl)-2-hydroxy-cyclohepta-2,4,6-trienone
C
3-(4-Chloro-benzyl)-2-hydroxy-cyclohepta-2,4,6-trienone
Conditions | Yield |
---|---|
In decalin at 190℃; for 14h; | A 15% B 3.5% C 59% |
2-(1-naphthylmethoxy)tropolone
A
2-hydroxy-2,4,6-cycloheptatrien-1-one
B
2-Hydroxy-5-naphthalen-1-ylmethyl-cyclohepta-2,4,6-trienone
C
2-Hydroxy-3-naphthalen-1-ylmethyl-cyclohepta-2,4,6-trienone
Conditions | Yield |
---|---|
In decalin at 190℃; for 7.5h; | A 5% B 20% C 52% |
In decalin at 190℃; for 7.5h; | A 5% B 20% C 52% |
In decalin at 153.1 - 180.1℃; for 7.5h; Kinetics; |
2-benzyloxycyclohepta-2,4,6-trienone
A
2-hydroxy-2,4,6-cycloheptatrien-1-one
B
3-benzyl-tropolone
C
5-benzyltropolone
Conditions | Yield |
---|---|
In decalin at 190℃; for 12h; | A 10% B 47% C 3.1% |
2-(4-bromophenylmethoxy)tropone
A
2-hydroxy-2,4,6-cycloheptatrien-1-one
B
5-(4-Bromo-benzyl)-2-hydroxy-cyclohepta-2,4,6-trienone
C
3-(4-Bromo-benzyl)-2-hydroxy-cyclohepta-2,4,6-trienone
Conditions | Yield |
---|---|
In decalin at 190℃; for 17h; | A 11% B 3.2% C 46% |
2-(4-methoxyphenylmethoxy)tropone
A
2-hydroxy-2,4,6-cycloheptatrien-1-one
B
2-Hydroxy-3-(4-methoxy-benzyl)-cyclohepta-2,4,6-trienone
C
2-Hydroxy-5-(4-methoxy-benzyl)-cyclohepta-2,4,6-trienone
Conditions | Yield |
---|---|
In decalin at 190℃; for 9h; | A 20% B 41% C 6.1% |
A
2-hydroxy-2,4,6-cycloheptatrien-1-one
Conditions | Yield |
---|---|
With boron trifluoride diethyl etherate for 17h; Heating; | A 40% B n/a |
A
2-hydroxy-2,4,6-cycloheptatrien-1-one
Conditions | Yield |
---|---|
In 1,2-dichloro-benzene at 180℃; for 0.5h; Mechanism; other 2-(2-furylmethoxy)tropones; | A n/a B 3% C 31% D 19% E 5% |
A
2-hydroxy-2,4,6-cycloheptatrien-1-one
Conditions | Yield |
---|---|
With boron trifluoride diethyl etherate for 17h; Heating; | A 23% B n/a |
2-(3-pentyloxy)tropone
A
(Z)-pent-2-ene
B
(E)-pent-2-ene
C
2-hydroxy-2,4,6-cycloheptatrien-1-one
D
butanone
Conditions | Yield |
---|---|
In dimethyl sulfoxide at 180℃; for 8h; | A 4% B 8% C n/a D 20% |
In dimethyl sulfoxide at 180℃; for 8h; | A n/a B 4% C n/a D 20% |
2-(2-butyloxy)tropone
A
(Z)-2-Butene
B
trans-2-Butene
C
2-hydroxy-2,4,6-cycloheptatrien-1-one
D
acetone
Conditions | Yield |
---|---|
In dimethyl sulfoxide at 180℃; for 8h; | A 7% B n/a C n/a D 5% |
In dimethyl sulfoxide at 180℃; for 8h; | A 5% B 7% C n/a D 7% |
In dimethyl sulfoxide at 180℃; for 8h; |
2-(2-Thienylmethoxy)tropone
A
2-hydroxy-2,4,6-cycloheptatrien-1-one
B
5-(2-Thienylmethyl)tropolone
C
3-(2-Thienylmethyl)tropolone
D
5-(2-Thienylmethyl)-2-(2-thienylmethoxy)tropone
E
3,5-Bis(2-thienylmethyl)tropolone
Conditions | Yield |
---|---|
In 1,2-dichloro-benzene for 1.5h; Product distribution; Mechanism; Heating; | A n/a B n/a C n/a D 6% E n/a |
Conditions | Yield |
---|---|
With N-Bromosuccinimide; chloroform und Erwaermen des Reaktionsprodukts auf 90-100grad; |
Conditions | Yield |
---|---|
With bromine; acetic acid und Erhitzen des Reaktionsprodukts unter vermindertem Druck; |
Conditions | Yield |
---|---|
With potassium acetate; acetic acid at 120 - 130℃; |
3-carboxytropolone
2-hydroxy-2,4,6-cycloheptatrien-1-one
Conditions | Yield |
---|---|
at 240 - 250℃; | |
With water at 160 - 170℃; | |
With pyridine at 135℃; |
6-hydroxy-5-oxo-cyclohepta-1,3,6-trienecarboxylic acid
2-hydroxy-2,4,6-cycloheptatrien-1-one
Conditions | Yield |
---|---|
With quinoline; copper |
Conditions | Yield |
---|---|
With potassium acetate; acetic acid at 120 - 130℃; |
Conditions | Yield |
---|---|
With potassium hydroxide; potassium permanganate |
7,7-dichlorobicyclo[3.2.0]hept-2-en-6-one
2-hydroxy-2,4,6-cycloheptatrien-1-one
Conditions | Yield |
---|---|
With sodium acetate In acetic acid |
2-(cyclohexyloxy)tropone
A
2-hydroxy-2,4,6-cycloheptatrien-1-one
B
cyclohexene
Conditions | Yield |
---|---|
In decalin at 180℃; for 4h; |
2-hydroxy-2,4,6-cycloheptatrien-1-one
benzyl bromide
2-benzyloxycyclohepta-2,4,6-trienone
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile Williamson etherification reaction; Heating; | 100% |
With tetra(n-butyl)ammonium hydroxide at 20℃; | 65% |
With perhydrodibenzo-18-crown-6; potassium carbonate In acetonitrile for 10h; Heating; | 50% |
With potassium carbonate In acetonitrile at 25℃; for 16h; Inert atmosphere; Reflux; |
2-hydroxy-2,4,6-cycloheptatrien-1-one
p-toluenesulfonyl chloride
2-(tosyloxy)tropone
Conditions | Yield |
---|---|
With pyridine at 20℃; | 100% |
With triethylamine In dichloromethane at 21℃; for 38h; | 99% |
In pyridine for 0.5h; | 98% |
2-hydroxy-2,4,6-cycloheptatrien-1-one
p-methoxybenzyl chloride
2-(4-methoxyphenylmethoxy)tropone
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile Williamson etherification reaction; Heating; | 100% |
Conditions | Yield |
---|---|
In pyridine | 99.5% |
2-hydroxy-2,4,6-cycloheptatrien-1-one
triethylaluminum
Et2Al(tropolonato)
Conditions | Yield |
---|---|
In diethyl ether N2-atmosphere; -78°C to room temp.; evapn. (vac.); elem. anal.; | 99% |
Conditions | Yield |
---|---|
With benzyltrimethylammonium tribromide; calcium carbonate In methanol; dichloromethane at 20℃; for 24h; Bromination; | 98% |
With bromine In methanol at 25℃; for 0.5h; | 95% |
With bromine In methanol at 25℃; for 0.5h; | 95% |
Conditions | Yield |
---|---|
In methanol byproducts: H2O; (Ar); std. Schlenk technique; tropolone was added to suspn. of W complexin MeOH; mixt. was heated at 50°C for 5 h; solvent removed (vac.); residie washed (hexane, ether); extd. (acetone);hexane added; kept at 0°C; | 98% |
4-(4-methoxyphenyl)-1-tosyl-1H-1,2,3-triazole
2-hydroxy-2,4,6-cycloheptatrien-1-one
Conditions | Yield |
---|---|
With dirhodium tetraacetate In 1,2-dichloro-ethane at 80℃; for 3h; Inert atmosphere; | 98% |
diazomethane
2-hydroxy-2,4,6-cycloheptatrien-1-one
2-methoxytropone
Conditions | Yield |
---|---|
In methanol; diethyl ether | 97% |
2-hydroxy-2,4,6-cycloheptatrien-1-one
(R,R)-(-)-1,6-bis(o-chlorophenyl)-1,6-diphenylhexa-2,4-diyne-1,6-diol
(1R,6R)-1,6-Bis-(2-chloro-phenyl)-1,6-diphenyl-hexa-2,4-diyne-1,6-diol; compound with 2-hydroxy-cyclohepta-2,4,6-trienone
Conditions | Yield |
---|---|
In hexane; benzene for 12h; Ambient temperature; | 97% |
2-hydroxy-2,4,6-cycloheptatrien-1-one
Conditions | Yield |
---|---|
With dirhodium tetraacetate In 1,2-dichloro-ethane at 80℃; for 2h; Inert atmosphere; | 97% |
Conditions | Yield |
---|---|
Stage #1: Zr(4+)*4C2O4(2-)*4K(1+) With oxalic acid; sodium carbonate In chloroform Stage #2: 2-hydroxy-2,4,6-cycloheptatrien-1-one In chloroform; water for 0.333333h; | 97% |
2-hydroxy-2,4,6-cycloheptatrien-1-one
Conditions | Yield |
---|---|
With potassium hydroxide In ethanol; water The boron compound, the organic compound, aqueous KOH and ethanol are mixed and added to a stirred solution of the Yb-salt in H2O, further stirring; filtn., drying in vac., recrystn. from methylene chloride/hexane mixture, elem. anal.; | 96% |
tris(2-oxy-3,5-di-tert-butylbenzyl)amino titanium(IV) tert-butoxide
2-hydroxy-2,4,6-cycloheptatrien-1-one
[nitrilotris(3,5-di-tert-butyl-2-cresolato)](tropolonato)titanium(IV)
Conditions | Yield |
---|---|
In benzene byproducts: t-butanol; ligand added to a soln. of Ti complex, stirred for 1 h; evapd. (vac.), dissolved in C6H6, MeCN added, mixed, crystd. for 24 h oncooling, filtered, washed (MeCN), dried (air); elem. anal.; | 96% |
2-hydroxy-2,4,6-cycloheptatrien-1-one
[(η-C5H5)2Mo(tropolonato)](tosyl)
Conditions | Yield |
---|---|
In methanol byproducts: H2O; (Ar); std. Schlenk technique; tropolone was added to suspn. of Mo complex in MeOH; mixt. was heated at 50°C for 5 h; solvent removed (vac.); residie washed (hexane, ether); extd. (acetone);hexane added; kept at 0°C; elem. anal.; | 96% |
Cyclohexyl isocyanide
pentanal
2-hydroxy-2,4,6-cycloheptatrien-1-one
benzylamine
2-[benzyl(7-oxo-1,3,5-cycloheptatrienyl)amino]-N1-cyclohexylhexanamide
Conditions | Yield |
---|---|
In methanol at 60℃; for 6h; Ugi-Smiles-type reaction; | 96% |
2-hydroxy-2,4,6-cycloheptatrien-1-one
Conditions | Yield |
---|---|
With dirhodium tetraacetate In 1,2-dichloro-ethane at 80℃; for 1h; Inert atmosphere; | 96% |
Conditions | Yield |
---|---|
With 18-crown-6 ether; potassium carbonate at 90℃; for 4h; | 96% |
2-hydroxy-2,4,6-cycloheptatrien-1-one
Conditions | Yield |
---|---|
With potassium hydroxide In ethanol; water The boron compound, the organic compound, aqueous KOH and ethanol are mixed and added to a stirred solution of the La-salt in H2O, further stirring; filtn., drying in vac., vac. sublimation at 250°C, elem. anal.; | 95% |
2-hydroxy-2,4,6-cycloheptatrien-1-one
boron tribromide
Conditions | Yield |
---|---|
In chloroform | 95% |
In chloroform |
Conditions | Yield |
---|---|
In not given byproducts: CH4; trimethyl metal deriv. reacts with an equimolr amt. of tropolone in ether, toluene or benzene at 25-40°C; purified by sublimation or recrystn. from toluene; identified by elem. anal., IR, NMR and mass spectra; | 95% |
1-(4-methylbenzensulfonyl)-4-phenyl-1H-1,2,3-triazole
2-hydroxy-2,4,6-cycloheptatrien-1-one
Conditions | Yield |
---|---|
With dirhodium tetraacetate In 1,2-dichloro-ethane at 80℃; for 1h; Catalytic behavior; Solvent; Inert atmosphere; | 95% |
Conditions | Yield |
---|---|
With thionyl chloride In benzene for 1.5h; Heating; | 94% |
With thionyl chloride In benzene at 95℃; for 2.5h; Inert atmosphere; | 94% |
With thionyl chloride In toluene at 120℃; for 1.5h; | 93% |
2-hydroxy-2,4,6-cycloheptatrien-1-one
bismuth(III) acetate
Conditions | Yield |
---|---|
In methanol; acetone for 3h; pH=Ca. 4; Reflux; | 93.2% |
2-hydroxy-2,4,6-cycloheptatrien-1-one
cis-[(2,2'-bipyridine)2Ru(tropolonate)](PF6)
Conditions | Yield |
---|---|
In ethanol stirring and refluxing Ru-complex with 2 equiv. of tropolone for 2 h (N2-atmosphere), filtration, addn. of aq. NH4PF6; collection, washing (EtOH, ether), drying in air; elem. anal.; | 93% |
In water stirring Ru-complex (75°C, 0.5 h), addn. of tropolone, stirring for 1 h, pptn. on addn. of NH4PF6; filtration, washing (H2O, Et2O), drying (vac.); elem. anal.; |
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