Welcome 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:108-67-8
Min.Order:1 Kilogram
Negotiable
Type:Manufacturers
inquiryOur clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
Dayangchem’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 quantiti
Cas:108-67-8
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Lab/Research institutions
inquiryItems Standard Result Appearance Colorless,transparent liquid Complies Content% ≥99.90
Cas:108-67-8
Min.Order:1 Kilogram
FOB Price: $3.0 / 10.0
Type:Manufacturers
inquiryProduct description: Product name Mesitylene CAS number 108-67-8 Assay ≥99% Appearance Colorless transparent liquid Capacity 1000mt/year Application Trimellitic acid, antioxi
Cas:108-67-8
Min.Order:1 Kilogram
FOB Price: $12.0
Type:Lab/Research institutions
inquiryhigh quality Good price Appearance:Colorless liquid Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea Port:China Main Port
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
Cas:108-67-8
Min.Order:1 Metric Ton
FOB Price: $1.0
Type:Manufacturers
inquiryHebei Yanxi Chemical Co., Ltd. is a professional research, development and production of lead acetate benzene acetamide enterprise backbone members by local well-known entrepreneurs and professional senior engineers in the party's "low car
Cas:108-67-8
Min.Order:1 Metric Ton
FOB Price: $1.0 / 2.0
Type:Trading Company
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
Products Name: 1,3,5 - three toluene CAS : 108-67-8 Molecular formula: C9H12 Molecular weight: Appearance : Colorless transparent liquid Usage : It is used in the p
Cas:108-67-8
Min.Order:5 Metric Ton
FOB Price: $1.0 / 2.0
Type:Other
inquiryOur company has been in existence for 10 years since its establishment. We have our own unique team. The company integrates independent research and development, production and sales. We have established famous brands at home and abroad. At present
Cas:108-67-8
Min.Order:1 Kilogram
FOB Price: $11.0 / 22.0
Type:Trading Company
inquiryProduct Detail Minimum Order Qty. 10 Gram
Cas:108-67-8
Min.Order:10 Gram
Negotiable
Type:Trading Company
inquiryMesitylene CAS:108-67-8 Specification ProName: 1,3,5-trimethylbenzene CasNo: 108-67-8 Molecular Formula: C9H12 Appearance: ask Application: intermediates DeliveryTime: Within 3 days after payment PackAge: foil aluminium bag/vacuum packing
Appearance:Store in a cool,dry place and keep away from direct strong light Storage:Store in a cool,dry place and keep away from direct strong light Package:As customer request Application:Used for research and industrial manu
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
Cas:108-67-8
Min.Order:0 Metric Ton
Negotiable
Type:Lab/Research institutions
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
A substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc
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
Superior quality Appearance:colourless liquid with an aromatic odour Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:1kg/bag, 1kg/drum or 25kg/drum or as per your request. Application:Organic synthetic raw materia
Product Details Grade: pharmaceutical grade Purity:99%+ ProductionCapacity: 1000 Kilogram/Month Scope of use: For scientific research only(The product must be used legally) Our Advantage 1. Best quality with competitive price. 2. Quick shipping,
Cas:108-67-8
Min.Order:1 Metric Ton
Negotiable
Type:Lab/Research institutions
inquiryWe are leading fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so on.Our main business covers the fields below: 1.Noble Metal Catalysts (Pt.Pd...)
Cas:108-67-8
Min.Order:1 Kilogram
FOB Price: $5.0
Type:Lab/Research institutions
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
Located in Hangzhou National Hi-Tech Industrial Development Zone, zhongqichem is a technical company mainly focus on the Custom synthesis, manufacturing, sales of chemicals to various industries. Benefiting from the outstanding customer service and h
SAGECHEM is a chemical R&D, manufacturing and distribution company in China since 2009, including pharmaceutical intermediates, agrochemical, dyestuff intermediates, organosilicone, API and etc. We also offer a full range of services in custom synthe
Capability on chemical synthesis1. Beijing High-Tech Enterprises2. Strong R&D Team3. 8 years of experiences in R & D of high-tech Catalyst;4. 5000 production techniques, 69 items of national patents, and 360 kinds of products on sales;5. The producti
high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
Jinhua huayi chemical co., ltd. is dedicated to the development, production and marketing of chemicals. On the basis of equality and mutual benefit, and under the principle of customer first, credit first, quality first, we are ready to join hands
Cas:108-67-8
Min.Order:100 Gram
Negotiable
Type:Lab/Research institutions
inquirygood quality and cheap price Package:25kg/200kg Application:as intermediates Transportation:by courier/sea/air
Cangzhou Enke Pharma Tech Co.,ltd. is located in Cangzhou City, Hebei province ,where is a famous petroleum chemical industry city?in China. Enke Pharma a high-tech enterprise ,and we are dedicated to developing and manufacturing new api,?intermediat
(2,4,6-trimethylphenyl) phenyl sulfone
A
Benzenesulfinic acid
B
1,3,5-trimethyl-benzene
Conditions | Yield |
---|---|
With lithium amalgam In N,N-dimethyl-formamide for 2h; Ambient temperature; | A 99% B 100% |
Conditions | Yield |
---|---|
electrlysis, at 1.5 V, electrolyte: tetrabutylammonium perchlorate, in CH2Cl2; | A 100% B 166 % |
In dichloromethane electrolysis, at 1.5 V; electrolyte: tetrabutylammonium perchlorate; | A 100% B 166 % |
morpholine
mesitylcopper(I)
A
C4H8NO(1-)*Cu(1+)
B
1,3,5-trimethyl-benzene
Conditions | Yield |
---|---|
In tetrahydrofuran THF, ambient temp., excess of amine;; evapd. or filtered; elem. anal.;; | A n/a B 100% |
mesitylcopper(I)
ammonia
A
amino-copper
B
1,3,5-trimethyl-benzene
Conditions | Yield |
---|---|
In tetrahydrofuran THF, ambient temp., excess of NH3;; evapd. or filtered; elem. anal.;; | A n/a B 100% |
2,4,6-trimethylphenyl(m-carboran-9-yl)iodonium tetrafluoroborate
sodium chloride
A
9-iodo-m-carborane
B
9-chloro-m-carborane
C
iodomesitylene
D
1,3,5-trimethyl-benzene
Conditions | Yield |
---|---|
In chloroform; water mixt. of aryl(m-carboran-9-yl)iodonium tetrafluoroborate, NaF, water and chloroform was vigorously stirred under reflux at 56°C, 2.5 h; internal standard (chlorobenzene) added and org. layer was analysed by GLC; | A 0% B 100% C 100% D 0% |
hexyl 2,4,6-trimethylbenzenesulfonate
A
1,3,5-trimethyl-benzene
B
hexan-1-ol
Conditions | Yield |
---|---|
With lithium amalgam In N,N-dimethyl-formamide; toluene Product distribution; Mechanism; further solvents; | A 85% B 99% |
Conditions | Yield |
---|---|
With potassium fluoride In tetrahydrofuran; water at 80℃; for 8h; Time; Schlenk technique; Sealed tube; Inert atmosphere; | 99% |
With [2-(di-tert-butylphosphinomethyl)-6-(diethylaminomethyl)pyridine]ruthenium(II) chlorocarbonyl hydride; isopropyl alcohol; sodium t-butanolate at 100℃; for 48h; Inert atmosphere; Sealed tube; Green chemistry; | 89% |
With isopropyl alcohol at 20℃; for 24h; UV-irradiation; chemoselective reaction; | 88% |
mesitylcopper(I)
N-butylamine
A
copper(I) n-butylamide
B
1,3,5-trimethyl-benzene
Conditions | Yield |
---|---|
In tetrahydrofuran THF, ambient temp., excess of amine;; evapd. or filtered; elem. anal.;; | A n/a B 98% |
dimesityl sulfone
A
2,4,6-trimethylbenzenesulphinic acid
B
1,3,5-trimethyl-benzene
Conditions | Yield |
---|---|
With lithium amalgam In N,N-dimethyl-formamide for 2h; Ambient temperature; | A 92% B 97% |
p-benzoquinone
2-mesitylmagnesium bromide
B
hydroquinone
C
1,3,5-trimethyl-benzene
Conditions | Yield |
---|---|
In tetrahydrofuran Grignard reaction; | A 97% B 3% C 4% |
mesitylcopper(I)
dibutylamine
A
copper(I) N,N-di-n-butylamide
B
1,3,5-trimethyl-benzene
Conditions | Yield |
---|---|
In tetrahydrofuran THF, ambient temp., stirring overnight;; evapd. in vac., washed with hexane, dried in vac., crystd. from hexane at -15°C; elem. anal.;; | A n/a B 95% |
2-methylchlorobenzene
mesitylboronic acid
A
2,2',4,6-tetramethylbiphenyl
B
1,3,5-trimethyl-benzene
Conditions | Yield |
---|---|
With potassium phosphate; tris(dibenzylideneacetone)dipalladium (0); tricyclohexylphosphine In toluene at 90℃; for 37h; Suzuki cross-coupling; Title compound not separated from byproducts.; | A 93% B 5% |
Conditions | Yield |
---|---|
With hydrogen iodide at -35℃; for 168000h; sealed tube; | A n/a B 92% |
mesitylcopper(I)
diethylamine
A
copper(I) N,N-diethylamide
B
1,3,5-trimethyl-benzene
Conditions | Yield |
---|---|
In tetrahydrofuran THF, ambient temp., excess of amine;; evapd. or filtered; elem. anal.;; | A n/a B 92% |
Conditions | Yield |
---|---|
With [Au(1,3-bis(2,6-diisopropylphenyl)-4,5-dihydroimidazol-2-ylidene)(O2CAd)] In toluene at 140℃; for 20h; | 90% |
With triethylsilane; palladium diacetate; 2,2-dimethylpropanoic anhydride; 1,4-di(diphenylphosphino)-butane In toluene at 160℃; for 15h; chemoselective reaction; | 90% |
With Nafion-H In toluene at 100℃; for 12h; | 80% |
piperidine
mesitylcopper(I)
A
copper piperidide
B
1,3,5-trimethyl-benzene
Conditions | Yield |
---|---|
In tetrahydrofuran THF, ambient temp., excess of amine;; evapd. or filtered; elem. anal.;; | A n/a B 90% |
hexyl 2,4,6-trimethylbenzenesulfonate
A
lithium 2,4,6-trimethylbenzenesulfinate
B
1,3,5-trimethyl-benzene
C
hexan-1-ol
Conditions | Yield |
---|---|
With lithium amalgam In 1,4-dioxane; toluene Product distribution; Mechanism; further solvents; | A 21% B 61% C 88% |
mesitylcopper(I)
aniline
A
copper(I) anilide
B
1,3,5-trimethyl-benzene
Conditions | Yield |
---|---|
In tetrahydrofuran THF, ambient temp., excess of aniline;; evapd. or filtered; elem. anal.;; | A n/a B 88% |
mesitylcopper(I)
tert-butylamine
A
copper(I) t-butylamide
B
1,3,5-trimethyl-benzene
Conditions | Yield |
---|---|
In tetrahydrofuran THF, ambient temp., excess of amine;; evapd. or filtered; elem. anal.;; | A n/a B 87% |
hexyl 2,4,6-trimethylbenzenesulfonate
A
2,4,6-trimethylbenzenesulphinic acid
B
1,3,5-trimethyl-benzene
C
hexan-1-ol
Conditions | Yield |
---|---|
With lithium amalgam In 1,4-dioxane at 23℃; for 2h; | A 69% B 10% C 85% |
A
C5H3F5
B
1,1,1-trifluoro-2-trifluoromethyl-2-butene
D
1,3,5-trimethyl-benzene
Conditions | Yield |
---|---|
In solid at 200℃; under 0.07 Torr; for 0.0125h; | A 11% B 48% C 3% D 83% |
2,4,6-trimethylphenyl bromide
trimethylstannane
A
n-butyltrimethyltin
B
1,3,5-trimethyl-benzene
Conditions | Yield |
---|---|
With n-butyllithium In hexane 2-bromomesitylene (1 equiv.) and TMTH (1 equiv.) in hexane cooled to 0°C under Ar, n-BuLi (1 equiv., 2.40 M in hexane) added, stirred for 5 h at reflux temp., quenched with water; analyzed by GC; | A 83% B 38% |
With n-butyllithium In hexane 2-bromomesitylene (1 equiv.) and TMTH (1 equiv.) in hexane cooled to 0°C under Ar, n-BuLi (1 equiv., 2.40 M in hexane) added, stirred for 15 min, quenched with water; analyzed by GC; | A 33% B 11% |
2,4,6-trimethylphenyl bromide
A
1-fluoro-2,4,6-trimethylbenzene
B
1,3,5-trimethyl-benzene
Conditions | Yield |
---|---|
Stage #1: 2,4,6-trimethylphenyl bromide With n-butyllithium In tetrahydrofuran; hexane at 0℃; Flow reactor; Stage #2: With N-fluorobis(benzenesulfon)imide In tetrahydrofuran; hexane at 0℃; Reagent/catalyst; Flow reactor; | A 82% B 10% |
Conditions | Yield |
---|---|
With chloro(1,5-cyclooctadiene)rhodium(I) dimer; triisopropyl phosphite; chlorotriisopropylsilane In ethyl-cyclohexane at 160℃; for 15h; Inert atmosphere; | 81% |
With chloro(1,5-cyclooctadiene)rhodium(I) dimer; triisopropyl phosphite; chlorotriisopropylsilane In ethylcyclohexane at 160℃; for 15h; Inert atmosphere; | 81% |
1-fluoro-2,4,6-trimethylbenzene
potassium enolate of acetone
A
1-(2,4,6-trimethylphenyl)-2-propanone
B
1-(2,4,6-Trimethylphenyl)-2-propanol
C
2,4,6-trimethylaniline
D
1,3,5-trimethyl-benzene
Conditions | Yield |
---|---|
With ammonia; potassium amide at -33℃; Product distribution; Rate constant; | A 2.8% B 5.6% C 11.7% D 80% |
With ammonia; potassium amide at -33℃; | A 1.8 % Chromat. B 3.1 % Chromat. C 18.2 % Chromat. D 77 % Chromat. |
With ammonia; potassium amide at -33℃; | A 2.8 % Chromat. B 5.6 % Chromat. C 11.7 % Chromat. D 80 % Chromat. |
B
1,3,5-trimethyl-benzene
Conditions | Yield |
---|---|
In diethyl ether complex is suspended in Et2O at room temp. for 2 d, thermal decomposition (N2); elem. anal.; | A 50% B 78% |
2,4,6-trimethylphenyl(m-carboran-9-yl)iodonium tetrafluoroborate
A
9-iodo-m-carborane
B
9-fluoro-m-carborane
C
iodomesitylene
D
1,3,5-trimethyl-benzene
Conditions | Yield |
---|---|
In chloroform; water mixt. of aryl(m-carboran-9-yl)iodonium tetrafluoroborate, NaF, water and chloroform was vigorously stirred under reflux at 56°C, 2.5 h; internal standard (chlorobenzene) added and org. layer was analysed by GLC; | A 16% B 78% C 75% D 14% |
1,3-dimethyl-5-methylenecyclohexane
1,3,5-trimethyl-benzene
Conditions | Yield |
---|---|
With n-butyllithium; potassium 2-methylbutan-2-olate Mechanism; 1) r.t., 16 h, 2) reflux, 6 h; further reagent: D2O; | 76% |
bis(mesitylene)vanadium(0)
A
Tetrakis(pyridin)-dichlorovanadin(II)
B
1,3,5-trimethyl-benzene
Conditions | Yield |
---|---|
With pyridine; 3-chloroprop-1-ene In toluene soln. of V-complex in toluene was treated with CH2=CHCH2Cl (inert atmosphere), the mixt. was stirred at room temp. for 24 h; the mother liquor contained org. compounds, products of the reaction of CH2=CHCH2Cl with either toluene or mesitylene (CLG-MS); filtered, ppt. was dissolved in pyridine, soln. was filtered and concd.to give the crystals of VCl2*4Py; identified by comparison of the IR spectrum with that of authentic sample; | A 75% B 75% |
methanol
acetone
A
pentamethylbenzene,
B
Hexamethylbenzene
C
1,3,5-trimethyl-benzene
Conditions | Yield |
---|---|
With aluminum oxide at 420℃; flowrate: 33 ml/ h; | A n/a B 74% C n/a |
Conditions | Yield |
---|---|
With iron oxide supported on HY zeolite In neat (no solvent) at 110℃; for 3h; Friedel-Crafts Acylation; | 100% |
With iodine; phosphorus trichloride at 160℃; for 36h; Inert atmosphere; | 99% |
With C4F9SO3H at 165℃; for 2h; | 98% |
Conditions | Yield |
---|---|
With heptafluorobutyric anhydride at 100℃; for 3h; Friedel-Crafts acetylation; | 100% |
With cross-linked polystyrene-supported aluminum triflate at 80℃; for 2.8h; Friedel-Crafts acylation; Neat (no solvent); chemoselective reaction; | 94% |
With trifluoromethylsulfonic anhydride at 20℃; for 0.0666667h; Friedel-Crafts acylation; | 93% |
Conditions | Yield |
---|---|
With hierarchical nanocrystalline zeolite ZSM-5 at 50℃; for 2h; Temperature; | 100% |
With iron(III) oxide at 20℃; for 0.166667h; Friedel Crafts acylation; regioselective reaction; | 96% |
With benzyltributylammonium tetrachloroferrate at 50℃; for 0.0666667h; Friedel-Crafts reaction; | 94% |
Conditions | Yield |
---|---|
With 5% Ru/MgO; hydrogen In tetrahydrofuran at 120℃; under 7600.51 Torr; for 8h; | 100% |
With Ti8O8(14+)*6C8H4O4(2-)*4O(2-)*3.3Li(1+)*0.7Co(2+)*0.7C4H8O*0.7H(1-); hydrogen In neat (no solvent) at 160℃; under 37503.8 Torr; for 18h; | 84% |
at 108℃; Thermodynamic data; Hydrogenation; |
Conditions | Yield |
---|---|
With dinitrogen tetraoxide In dichloromethane at -78℃; for 3h; Irradiation; | 100% |
With dinitrogen tetraoxide In dichloromethane at 25℃; for 24h; | 100% |
With nitric acid; sulfuric acid In dichloromethane at 25℃; for 0.03h; | 100% |
Conditions | Yield |
---|---|
With hydrogenchloride; sodium peroxide In acetic acid at 20 - 25℃; for 4h; | 100% |
With 1-Cl+SbCl6- In dichloromethane at 25℃; for 1h; | 98% |
With sodium chlorite; trichloroacetic acid In dichloromethane at 20℃; for 1h; Chlorination; | 95% |
formaldehyd
1,3,5-trimethyl-benzene
1,3,5-tris(bromomethyl)-2,4,6-trimethylbenzene
Conditions | Yield |
---|---|
With hydrogen bromide; acetic acid at 95℃; for 12h; | 100% |
With hydrogen bromide; acetic acid at 95℃; for 12h; Inert atmosphere; | 99% |
With sulfuric acid; potassium bromide In acetic acid at 90 - 95℃; for 6h; | 97% |
4-aminofuroxan-3-carboxylic acid azide
1,3,5-trimethyl-benzene
3-azidocarbonyl-4-(2,4,6-trimethylphenylazo)furoxan
Conditions | Yield |
---|---|
Stage #1: 4-aminofuroxan-3-carboxylic acid azide With phosphoric acid; sulfuric acid; sodium nitrite at 0 - 2℃; for 1h; Stage #2: 1,3,5-trimethyl-benzene In pyridine at 0 - 20℃; | 100% |
Conditions | 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% |
1,3,5-trimethyl-benzene
4-n-methylphenylacetylene
1-(4-methylphenyl)-1-(2,4,6-trimethylphenyl)ethene
Conditions | Yield |
---|---|
With trifluoroacetic acid In dichloromethane at 30℃; for 24h; Cooling with ice; | 100% |
With Cu-exchanged tungstophosphoric acid at 80℃; for 3h; neat (no solvent); regioselective reaction; | 91% |
With trifluorormethanesulfonic acid; copper(II) bis(trifluoromethanesulfonate) at 20℃; for 20h; | 84% |
tri-μ-chlorobis[(.eta-benzene)ruthenium(II)] tetrafluoroborate
1,3,5-trimethyl-benzene
Conditions | Yield |
---|---|
In water; trifluoroacetic acid under dry conditions mixt. of Ru complex, mesitylene, and CF3COOH refluxed for 1.5 h, 48% aq. HBF4 added; pptd. by careful addn. of Et2O; elem. anal.; | 100% |
bis(pentafluorophenyl)(η6-anisole)cobalt(II)
1,3,5-trimethyl-benzene
Conditions | Yield |
---|---|
In chloroform-d1 byproducts: anisole; mol. ratio 1/1; not isolated, detected by NMR; | 100% |
Conditions | Yield |
---|---|
With Ag3(μ2-(3,5-(CF3)2PyrPy))3 In dichloromethane at 20℃; Buchner Ring Enlargement; | 100% |
With dirhodium tetraacetate In dichloromethane at 25℃; for 60h; Buchner Ring Enlargement; Inert atmosphere; | 77% |
Stage #1: 1,3,5-trimethyl-benzene With dirhodium tetraacetate In dichloromethane Inert atmosphere; Stage #2: diazoacetic acid ethyl ester In dichloromethane at 23℃; for 60h; Inert atmosphere; | 77% |
1,3,5-trimethyl-benzene
Conditions | Yield |
---|---|
In pentane at 20℃; Inert atmosphere; | 100% |
1,3,5-trimethyl-benzene
Conditions | Yield |
---|---|
With trifluorormethanesulfonic acid In dichloromethane at 20℃; for 24h; Inert atmosphere; | 100% |
In 2,2,2-trifluoroethanol at 20℃; for 24h; | 89% |
1,3,5-trimethyl-benzene
Conditions | Yield |
---|---|
With trifluorormethanesulfonic acid at 50℃; for 16h; | 100% |
Conditions | Yield |
---|---|
With indium(III) triflate; lithium perchlorate In nitromethane at 20℃; | 99% |
With antimonypentachloride; lithium perchlorate In dichloromethane for 0.5h; Heating; | 95% |
With nano-sulfated titania at 50℃; for 1h; Friedel Crafts acylation; neat (no solvent); | 95% |
Conditions | Yield |
---|---|
With trifluoroacetic anhydride; bismuth(lll) trifluoromethanesulfonate at 30℃; for 12h; Friedel-Crafts acetylation; | 99% |
With pyridin-2-yl trifluoromethanesulfonate; trifluoroacetic acid for 5h; Heating; | 96% |
With cross-linked polystyrene-supported aluminum triflate at 80℃; for 2.9h; Friedel-Crafts acylation; Neat (no solvent); chemoselective reaction; | 93% |
Conditions | Yield |
---|---|
With tetrafluoroboric acid; [bis(pyridine)iodine]+ tetrafluoroborate In diethyl ether; dichloromethane for 0.1h; Ambient temperature; | 99% |
With Oxone; potassium iodide In methanol at 20℃; for 24h; | 99% |
With ammonium nitrate; sulfuric acid; iodine In water; acetonitrile at 60℃; for 0.166667h; regioselective reaction; | 98% |
1,3,5-trimethyl-benzene
2,4-diiodomesitylene
Conditions | Yield |
---|---|
With N,N,N-trimethylbenzenemethanaminium dichloroiodate; zinc(II) chloride In acetic acid at 70℃; for 28h; | 99% |
With iodine; 1-(p-methylbenzenesulfonyloxy)-1,2-benziodoxol-3(1H)-one In acetonitrile for 18h; Ambient temperature; | 99% |
With iodine; 1-(p-methylbenzenesulfonyloxy)-1,2-benziodoxol-3(1H)-one In acetonitrile for 16h; Ambient temperature; | 99% |
Conditions | Yield |
---|---|
With N-Bromosuccinimide; perchloric acid In tetrachloromethane for 22h; Ambient temperature; | 99% |
With hydrogen bromide; dihydrogen peroxide In water at 20℃; for 24h; Darkness; | 98% |
With gold(III) chloride; N-Bromosuccinimide In dichloromethane at 20℃; for 12h; Inert atmosphere; | 98% |
4-methyl-benzoyl chloride
1,3,5-trimethyl-benzene
2,4,6,4'-tetramethylbenzophenone
Conditions | Yield |
---|---|
With C4F9SO3H at 165℃; for 2h; | 99% |
With In(OSO2CF3)3 for 0.0666667h; Friedel-Crafts acylation reaction; microwave irradiation; | 88% |
With copper(II) ferrite In neat (no solvent) at 80℃; for 18h; Friedel-Crafts Acylation; | 79% |
Conditions | Yield |
---|---|
With sulfuric acid; trifluoroacetic anhydride | 99% |
With trifluoromethylsulfonic anhydride; bis(N-methylpyridinium) sulfate for 0.0833333h; | 95% |
1,3,5-trimethyl-benzene
A
4-nitro-o-xylene
B
2-nitro-2',4,4',5,6'-pentamethylbiphenyl
Conditions | Yield |
---|---|
With boron trifluoride diethyl etherate In dichloromethane at 20℃; for 0.0166667h; | A 1% B 99% |
About|Contact|Cas|Product Name|Molecular|Country|Encyclopedia
Message|New Cas|MSDS|Service|Advertisement|CAS DataBase|Article Data|Manufacturers | Chemical Catalog
©2008 LookChem.com,License: ICP
NO.:Zhejiang16009103
complaints:service@lookchem.com Desktop View