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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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
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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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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
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inquiryAbout Product Details
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inquiryWith our good experience, we offer detailed technical support and advice to assist customers. We communicate closely with customers to establish their quality requirements. Consistent Quality Our plant has strict quality control in each manufacturin
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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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
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inquiryName: 2,4,6-Trimethylbenzoic acid Synonyms: Mesitylenecarboxylic acid CAS:480-63-7 MF: C10H11O2 Appearance: white powder Storage:Store in cool and dry place, away from sun light. Package: 25kgs/drum Application:Organic synthesis Transportati
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inquiry1.In No Less 10 years exporting experience. you 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 Specializ
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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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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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inquiryBest quality & Attractive price & Professional service; Trial & Pilot & Commercial Hisunny Chemical is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality intermediates, specia
1. 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
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inquiryEnglish name: 2,4, 6-trimethylbenzoic acid Chinese alias name: homo trimethylbenzoic acid English name: 2,4, 6-trimethylbenzoic acid English alias: Mesitylenecarboxylic acid;Mesitoic acid; Mesitylene-2-carboxylic acid; 2 minus 2 - Trimethyl Benzoi
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inquiryHangzhou 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
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inquiryJ&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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inquiryChemlyte Solutions believe that customers and suppliers deserve much more than what traditional distributors can offer. To grow in today s fast-paced and increasingly competitive market it is essential to be able to quickly adapt to market forces eff
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inquiryWe are one of a few suppliers that can offer custom synthesis service of this product We are specialized in custom synthesis, chemical/pharmaceutical/ pesticides outsourcing and contract research. We are committed to prov
Cas:480-63-7
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inquirySuperior quality, moderate price & quick delivery. Appearance:White crystalline powder Storage:Room temperature, tight from air Package:25kg/drum, or as per your request. Application:For medicine , pesticide intermediates Transportation:as per
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inquiry2,4,6-trimethylbenzoic acid Melting point 152-155 °C (lit.) Storage conditions Store below +30°C. BRN 1866187 InChIKey FFFIRKXTFQCCKJ-UHFFFAOYSA-N CAS Database 480-63-7 (CAS DataBase Reference) NIST Chemical Information Benzoic
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inquiryGMP standard, high purity, competitive price, in stock 1. Quick Response: within 6 hours after receiving your email. 2. Quality Guarantee: All products are strictly tested by our QC, confirmed by QA, and approved by a third-party lab in China, USA,
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inquiry2,4,6-Trimethylbenzoic acid Chemical Properties Melting point 152-155 °C (lit.) Boiling point 288.61°C (estimate) density 1.0670 (estimate) refractive index 1.5198 (estimate) storage temp. Store below +30°C. pka pK1
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inquiryfactory?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
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inquiryProduct name: 2,4,6-Trimethylbenzoic Acid CAS No.: 480-63-7 Molecule Formula:C10H11O2 Molecule Weight:163.19 Purity: 99.0% Package: 25kg/drum Description:White or off-white powder Manufacture Standards:Enterprise Standard
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inquiryShandong 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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inquiryCHENGDU YANXI is a comprehensive manufacturer and an international distribution of products throughout the world. Specialized in Scrap metal, Chemical raw materials, Paper products and color industry. We aim to become leading position in global dis
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inquiryConditions | Yield |
---|---|
With Et3SiB(C6F5)4 at 20℃; under 22502.3 Torr; for 18h; Reagent/catalyst; | 100% |
With aluminum tri-bromide; Triphenylsilyl chloride at 20℃; under 22502.3 Torr; for 3h; Autoclave; | 97% |
With aluminum (III) chloride at 30℃; under 15001.5 Torr; for 5h; Pressure; Temperature; | 95.2% |
Conditions | Yield |
---|---|
Stage #1: carbon dioxide; 2-mesitylmagnesium bromide In tetrahydrofuran at 20℃; under 3000.3 Torr; gas-liquid flow reactor assembly; Stage #2: With polymer-supported sulfonic acid In tetrahydrofuran | 100% |
In tetrahydrofuran at 1℃; for 0.0833333h; | 74% |
2,4,6-trimethyl-benzoic acid-anhydride
A
2,4,6-trimethylbenzyl alcohol
B
mesitylenecarboxylic acid
Conditions | Yield |
---|---|
With Li(1+)*C12H28AlO3(1-) In tetrahydrofuran; hexane at -78℃; for 1h; | A 99% B 98% |
Conditions | Yield |
---|---|
With C4H11FeMo6NO24(3-)*3C16H36N(1+); water; oxygen; sodium carbonate at 50℃; under 760.051 Torr; for 8h; Green chemistry; | 99% |
With 4H3N*4H(1+)*CuMo6O18(OH)6(4-); water; oxygen; sodium carbonate at 50℃; under 760.051 Torr; for 12h; | 99% |
With tris[2-(4,6-difluorophenyl)pyridinato-C2,N]-iridium(III); oxygen In acetonitrile at 20℃; Irradiation; Sealed tube; Green chemistry; chemoselective reaction; | 90% |
Conditions | Yield |
---|---|
With dihydrogen peroxide In water; toluene at 20 - 85℃; for 4h; | 98% |
With diethylene glycol dimethyl ether at 70℃; for 0.5h; Sonication; | 93% |
With potassium phosphate; carbon dioxide; CrH6Mo6O24(3-)*3H3N*3H(1+) In dimethyl sulfoxide at 80℃; under 750.075 Torr; for 24h; Green chemistry; | 84% |
carbon dioxide
2,4,6-trimethylbenzeneboronic acid neopentyl glycol cyclic ester
mesitylenecarboxylic acid
Conditions | Yield |
---|---|
With potassium tert-butylate; copper(l) chloride; 1,3-bis[2,6-diisopropylphenyl]imidazolium chloride In tetrahydrofuran at 70℃; under 760.051 Torr; for 24h; | 98% |
Conditions | Yield |
---|---|
With tetra(n-butyl)ammonium hydroxide In tetrahydrofuran; water at 70℃; for 1h; | 97% |
With potassium hydroxide; Aliquat 336 at 200℃; for 0.0833333h; microwave irradiation; | 95% |
With Me2AlTeMe In toluene at 23℃; for 6h; | 91% |
n-octyl mesitoate
mesitylenecarboxylic acid
Conditions | Yield |
---|---|
With sodium hydroxide; Aliquat 336 at 200℃; for 0.0833333h; microwave irradiation; | 97% |
Trichloroacetyl chloride
1,3,5-trimethyl-benzene
mesitylenecarboxylic acid
Conditions | Yield |
---|---|
Stage #1: trifluoroacetyl chloride; 1,3,5-trimethyl-benzene With aluminum (III) chloride at 0 - 10℃; for 2h; Inert atmosphere; Stage #2: With hydrogenchloride In water Temperature; | 95% |
mesitylenecarboxylic acid
Conditions | Yield |
---|---|
With water; N,N-dimethyl-formamide at 70℃; for 3h; Green chemistry; chemoselective reaction; | 94% |
With N,N,N',N'-tetramethylguanidine In acetonitrile at 50℃; for 1h; | 92% |
Conditions | Yield |
---|---|
With dipotassium peroxodisulfate; (4-CH3O-C6H4-N-CH2)2PO3SCF3; palladium(II) trifluoroacetate In trifluoroacetic acid at 30℃; for 48h; | 93% |
mesitylenecarboxylic acid
Conditions | Yield |
---|---|
With water; N,N-dimethyl-formamide at 70℃; for 3h; Green chemistry; chemoselective reaction; | 93% |
mesitylenecarboxylic acid
Conditions | Yield |
---|---|
With sodium hydride In N,N-dimethyl-formamide at 20℃; | 92% |
methyl 2,4,6-trimethylbenzoate
diphenyl diselenide
A
mesitylenecarboxylic acid
B
selenoanisole
Conditions | Yield |
---|---|
Stage #1: diphenyl diselenide With aluminum (III) chloride; zinc In acetonitrile at 70℃; under 760.051 Torr; for 1.25h; Neutral; Stage #2: methyl 2,4,6-trimethylbenzoate In acetonitrile at 70℃; under 760.051 Torr; for 6h; Neutral; | A 92% B n/a |
Conditions | Yield |
---|---|
With Me2AlTeMe In toluene at 23℃; for 12h; | 89% |
With dichloro bis(acetonitrile) palladium(II); cyclopentadienylruthenium(II) trisacetonitrile hexafluorophosphate; diethylene glycol dimethyl ether; 1,6-bis(diphenylphosphino)hexane; water In 1,2-dimethoxyethane; dichloromethane at 20 - 85℃; for 1.33333h; Inert atmosphere; | 26 %Chromat. |
Conditions | Yield |
---|---|
With C26H30B10Cl2P2Pd In toluene at 80℃; under 760.051 Torr; for 8h; | 89% |
With copper(l) iodide; diethylzinc; N,N`-dimethylethylenediamine In dimethyl sulfoxide at 25℃; under 760.051 Torr; | 61% |
carbon dioxide
1,3,5-trimethyl-benzene
A
mesitylenecarboxylic acid
B
dimesityl ketone
Conditions | Yield |
---|---|
With chloro-trimethyl-silane; aluminum tri-bromide at 20℃; under 22501.8 Torr; for 3h; | A 87% B 6% |
With chloro-trimethyl-silane; aluminum tri-bromide at 20℃; under 22502.3 Torr; for 3h; Autoclave; | A 87% B 6% |
With Et3SiB(C6F5)4 at 20℃; under 22502.3 Torr; for 18h; Reagent/catalyst; Friedel-Crafts Acylation; | A 86% B 14% |
With aluminum tri-bromide under 44130.5 Torr; |
Conditions | Yield |
---|---|
With Me2AlTeMe In toluene at 23℃; for 14h; | 87% |
With methanol; sodium tetrahydroborate; nickel(II) chloride hexahydrate at 20℃; for 0.25h; chemoselective reaction; | 85% |
sodium methyl carbonate
2-mesitylmagnesium bromide
mesitylenecarboxylic acid
Conditions | Yield |
---|---|
In diethyl ether at 20℃; for 24h; Inert atmosphere; | 85% |
carbon dioxide
2,4,6-trimethylbenzenesulfonate sodium salt
mesitylenecarboxylic acid
Conditions | Yield |
---|---|
Stage #1: carbon dioxide; 2,4,6-trimethylbenzenesulfonate sodium salt With copper(l) iodide; potassium tert-butylate; o-phenanthroline In dimethyl sulfoxide at 140℃; under 760.051 Torr; for 12h; Schlenk technique; Stage #2: With hydrogenchloride In water; dimethyl sulfoxide Schlenk technique; | 82% |
carbon dioxide
sodium 2,4,6-trimethylbenzenesulfinic acid
mesitylenecarboxylic acid
Conditions | Yield |
---|---|
With copper(l) iodide; 1,10-Phenanthroline; potassium tert-butylate In dimethyl sulfoxide at 140℃; under 750.075 Torr; for 3h; Schlenk technique; Sealed tube; | 82% |
A
4-hydroxy-1-phenyl-butan-1-one
B
mesitylenecarboxylic acid
C
butyrophenone
D
3,4-dihydronaphthalene-1(2H)-one
Conditions | Yield |
---|---|
With iron(II) sulfate In tetrahydrofuran; water at 20℃; for 16h; | A 9% B 81% C 26% D 13% |
mesitylenecarboxylic acid
Conditions | Yield |
---|---|
With chloro-trimethyl-silane; sodium iodide In acetonitrile at 20℃; for 1h; Substitution; | 80% |
Conditions | Yield |
---|---|
With oxygen; manganese (II) acetate tetrahydrate; cobalt(II) diacetate tetrahydrate In acetic acid at 100℃; under 760.051 Torr; for 15h; | 78% |
With permanganate(VII) ion anschl. Behandeln mit Schwefelsaeure; | |
Multi-step reaction with 2 steps 1: KMnO4; alkali 2: bei der Destillation View Scheme |
carbon dioxide
2,4,6-trimethylphenyl trifluoromethanesulfonate
mesitylenecarboxylic acid
Conditions | Yield |
---|---|
Stage #1: carbon dioxide; 2,4,6-trimethylphenyl trifluoromethanesulfonate With manganese; [Co(2,9-dimethyl-1,10-phenanthroline)I2] In N,N-dimethyl acetamide at 40℃; under 760.051 Torr; for 20h; Schlenk technique; Stage #2: With hydrogenchloride In diethyl ether; water at 20℃; for 0.166667h; Temperature; Reagent/catalyst; Schlenk technique; | 77% |
With (4,4'-di-tert-butyl-2,2'-dipyridyl)-bis-(2-phenylpyridine(-1H))-iridium(III) hexafluorophosphate; palladium diacetate; caesium carbonate; N-ethyl-N,N-diisopropylamine; DavePhos In N,N-dimethyl acetamide at 20℃; for 36h; Irradiation; Green chemistry; chemoselective reaction; | 75% |
With (2’,4’,6’-triisopropyl-[1,1’-biphenyl]-2-yl)-diphenylphosphine; bis(2-phenylpyridinato)(2,2'-bipyridine)iridium(III) hexafluorophosphate; tetrabutylammomium bromide; palladium diacetate; caesium carbonate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl acetamide at 20℃; under 760.051 Torr; for 4h; Irradiation; |
[(3R,4S)-2-(4-Nitro-phenyl)-5-phenyl-4-(2,4,6-trimethyl-benzoyl)-3,4-dihydro-2H-pyrazol-3-yl]-(2,4,6-trimethyl-phenyl)-methanone
A
mesitylenecarboxylic acid
B
[1-(4-Nitro-phenyl)-3-phenyl-1H-pyrazol-4-yl]-(2,4,6-trimethyl-phenyl)-methanone
Conditions | Yield |
---|---|
at 200℃; for 0.166667h; | A 65% B 75% |
Conditions | Yield |
---|---|
With oxygen; potassium hydroxide at 20℃; Schlenk technique; chemoselective reaction; | A 62% B 63% |
[(3R,4S)-2,5-Di-p-tolyl-4-(2,4,6-trimethyl-benzoyl)-3,4-dihydro-2H-pyrazol-3-yl]-(2,4,6-trimethyl-phenyl)-methanone
A
mesitylenecarboxylic acid
B
(1,3-Di-p-tolyl-1H-pyrazol-4-yl)-(2,4,6-trimethyl-phenyl)-methanone
Conditions | Yield |
---|---|
at 200℃; for 0.166667h; | A 30% B 55% |
2-(2,4,6-trimethylphenyl)-2-hydroxyacetonitrile
A
mesytaldehyde
B
mesitylenecarboxylic acid
Conditions | Yield |
---|---|
Stage #1: 2-hydroxy-2-(2,4,6-trimethylphenyl)acetonitrile With (η(6)-benzene)chloro[1,2-bis(diphenylphosphino)ethane]ruthenium(II) chloride In benzene at 120℃; for 24h; Inert atmosphere; Schlenk technique; Stage #2: With water In dichloromethane; ethyl acetate; benzene for 24h; | A 40% B 55% |
diazomethane
mesitylenecarboxylic acid
methyl 2,4,6-trimethylbenzoate
Conditions | Yield |
---|---|
In diethyl ether | 100% |
With diethyl ether |
Conditions | Yield |
---|---|
With sulfuric acid at 148 - 159℃; under 9375.7 Torr; for 0.0866667h; Irradiation; | 100% |
With dmap; dicyclohexyl-carbodiimide | |
With fluorosulphonic acid at -70℃; Yield given; | |
With sulfuric acid at 20℃; for 48h; | |
With sulfuric acid at 100℃; for 24h; |
Conditions | Yield |
---|---|
With caesium carbonate In acetonitrile for 2h; Heating; | 100% |
With cesium fluoride In acetonitrile for 1h; Heating; | 99% |
With 1,8-diazabicyclo[5.4.0]undec-7-ene In benzene | |
With potassium carbonate In acetone for 16h; Heating; | |
With cesium fluoride In N,N-dimethyl-formamide at 10 - 15℃; for 24h; | 88 % Chromat. |
mesitylenecarboxylic acid
methyl 6'-O-butyryl-β-lactoside
methyl 6'-O-butyryl-2,2',3,3',4',6-hexa-O-mesitoyl-β-lactoside
Conditions | Yield |
---|---|
With trifluoroacetic anhydride In benzene for 2h; Ambient temperature; | 100% |
Conditions | Yield |
---|---|
With diphosphorus tetraiodide In tetrachloromethane; dichloromethane Heating; | 100% |
With ethylene dichloride hydrochloride; triethylamine In dichloromethane at 0 - 20℃; for 6h; |
mesitylenecarboxylic acid
Conditions | Yield |
---|---|
With potassium tert-butylate In methanol at 20℃; for 4h; | 100% |
With potassium tert-butylate In methanol for 4h; | 82% |
2-iodo-propane
mesitylenecarboxylic acid
isopropyl 2,4,6-trimethylbenzoate
Conditions | Yield |
---|---|
With N(Et)4(1+)*(2-pyrrolidone-anion) In N,N-dimethyl-formamide for 1h; Ambient temperature; | 99% |
With caesium carbonate In acetonitrile for 2h; Heating; | 96% |
With potassium carbonate In acetone for 16h; Heating; |
dichloromethane
mesitylenecarboxylic acid
Methylendi-<2,4,6-trimethylbenzoesaeure>-ester
Conditions | Yield |
---|---|
With potassium carbonate In dimethyl sulfoxide at 130℃; for 5h; | 99% |
With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate |
Conditions | Yield |
---|---|
With silver carbonate; palladium(II) trifluoroacetate In dimethyl sulfoxide; N,N-dimethyl-formamide at 120℃; for 1.5h; Heck olefination; | 99% |
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile for 4h; Heating; | 99% |
mesitylenecarboxylic acid
trimethylaluminum
[Me2Al(μ-2,4,6-trimethylbenzoate)]2
Conditions | Yield |
---|---|
In hexane byproducts: CH4; in a glovebox, Al-contg. compd. (2.00 mmol) was slowly added to a cooledhexane suspn. (-35.degree C) of carboxylic acid (2.00 mmol); stirring a t ambient temp. for 3 h; the solvent was removed in vac.; elem. anal.; | 99% |
Conditions | Yield |
---|---|
With potassium carbonate In toluene at 20℃; for 2h; Inert atmosphere; | 99% |
mesitylenecarboxylic acid
N-(2-methylbenzoyl)-8-aminoquinoline
Conditions | Yield |
---|---|
With cobalt(II) acetate; sodium carbonate; silver sulfate In 1,2-dichloro-ethane at 80℃; for 24h; Inert atmosphere; Sealed tube; regioselective reaction; | 99% |
mesitylenecarboxylic acid
aniline
N-(2,4,6-trimethylphenyl)-N'-phenylurea
Conditions | Yield |
---|---|
With diphenyl phosphoryl azide; triethylamine In toluene at 100℃; for 0.0166667h; Curtius Rearrangement; Microwave irradiation; | 99% |
mesitylenecarboxylic acid
1,2-diamino-benzene
2-(2,4,6-trimethylphenyl)-1H-benzoimidazole
Conditions | Yield |
---|---|
With Eaton’s reagent at 140℃; for 0.5h; Inert atmosphere; | 98.6% |
With Eaton′s Reagent at 120 - 140℃; for 0.5h; Inert atmosphere; | 98.6% |
With polyphosphoric acid at 200℃; for 2h; | 80% |
With polyphosphoric acid at 120 - 150℃; for 16h; | 62% |
Conditions | Yield |
---|---|
With potassium hydroxide; Aliquat 336 at 60℃; for 1h; | 98% |
With potassium carbonate In acetone at 100℃; for 0.166667h; microwave irradiation; | 94% |
With tetradecyl(trihexyl)phosphonium bistriflamide; N-ethyl-N,N-diisopropylamine at 30℃; | 86% |
mesitylenecarboxylic acid
benzylamine
N-benzyl-2,4,6-trimethylbenzamide
Conditions | Yield |
---|---|
With TEA; diphenyl (2,3-dihydro-2-thioxo-3-benzoxazolyl)phosphonate In various solvent(s) for 2h; Ambient temperature; | 98% |
With 1-methyl-pyrrolidin-2-one; 3,3'-(phenylphosphinylidene)bis<2(3H)-benzothiazolone; triethylamine Ambient temperature; | 91% |
Conditions | Yield |
---|---|
With pyridine at 115℃; for 0.5h; | 98% |
Conditions | Yield |
---|---|
With potassium hydroxide; Aliquat 336 at 20℃; for 1h; | 98% |
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 24h; Inert atmosphere; | 88% |
Conditions | Yield |
---|---|
With caesium carbonate In acetonitrile for 0.5h; Heating; | 98% |
With potassium fluoride; tetra(n-butyl)ammonium hydrogensulfate In tetrahydrofuran at 20℃; for 72h; Inert atmosphere; | 98% |
mesitylenecarboxylic acid
Triethyl orthoacetate
ethyl 2,4,6-trimethylbenzoate
Conditions | Yield |
---|---|
microwave irradiation; | 98% |
In various solvent(s) at 80℃; for 1.5h; | 96% |
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran at 20℃; for 6h; | 98% |
mesitylenecarboxylic acid
yttrium tris(2,4,6-trimethylbenzoate)
Conditions | Yield |
---|---|
In tetrahydrofuran byproducts: HN(SiMe3)2; under vac.; to a soln. of Y-contg. compd. (1.50 mmol) in THF was slowly added a soln. of carboxylic acid (4.50 mmol) in THF at -45°C; stirring at ambient temp. overnight (16 h); the solvent and volatiles were removed in vac.; solid was washed severaltimes with hexane; drying for several hours; elem. anal.; | 98% |
In tetrahydrofuran Ar-atmosphere; stirring for 20 min; evapn. (reduced pressure), washing (PhMe, hexanes); | 54% |
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile at 80℃; for 3h; Inert atmosphere; | 98% |
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