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
Cas:717-74-8
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inquiryProduct description: Product name 1,3,5-Triisopropylbenzene CAS number 717-74-8 Assay ≥98% Appearance Light yellow liquid Capacity 100mt/year Application Organic intermediate
Cas:717-74-8
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inquiryhigh quality Appearance:White or off white powder 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:shanghai
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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inquiryTIANFUCHEM--717-74-8--1,3,5-Triisopropylbenzene factory price Our company was built in 2009 with an ISO certificate.In the past 10 years, we have grown up as a famous fine chemicals supplier in China And we had established stable business
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inquiryName:1,3,5-Triisopropylbenzene CAS:717-74-8 Appearance:Transparent colorless liquid Application:Pharmaceutical Intermediates Appearance:Colorless transparent liquid Storage:Preserve in well-closed, light-resistant and airtight co
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inquiry1,3,5-Triisopropylbenzene CAS:717-74-8 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
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Min.Order:1 Gram
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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
Appearance:White or off white powder Storage:Store in a cool,dry place and keep away from direct strong light Package:As customer request Application:Organic synthesis Transportation:Common products:Sea/Air/Courier Dangerous Ch
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Min.Order:100 Metric Ton
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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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inquiryA 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
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inquiryZibo 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
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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
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inquirySuperior quality, moderate price & quick delivery. Appearance:colourless liquid Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:25kg/drum, or as per your request. Application:Used as Pharmaceutical Interme
Our 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
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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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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
Cas:717-74-8
Min.Order:1 Metric Ton
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Type:Trading Company
inquiryProduct Name: 1,3,5-triisopropylbenzene English alias: 1,3,5-tri (propan-2-yl) benzene; benzene, 1,3,5-tris (1-methylethyl) -; CAS No.: 717-74-8 Molecular formula: C15H24 Molecular weight: 204
Cas:717-74-8
Min.Order:10 Gram
Negotiable
Type:Lab/Research institutions
inquiry2,4,6-triisopropyl-benzenesulfonic acid n-hexylester
A
1,3,5-triisopropyl benzene
B
hexan-1-ol
Conditions | Yield |
---|---|
With lithium amalgam In N,N-dimethyl-formamide; toluene Product distribution; Mechanism; further solvents; | A 100% B 100% |
N,N-dibenzyl-2,4,6-triisopropylbenzenesulfonamide
A
1,3,5-triisopropyl benzene
B
dibenzylamine
Conditions | Yield |
---|---|
With titanium(IV) isopropylate; chloro-trimethyl-silane; magnesium In tetrahydrofuran at 50℃; Inert atmosphere; | A 99% B 93% |
2,4,6-triisopropylphenylboronic acid
1,3,5-triisopropyl benzene
Conditions | Yield |
---|---|
With [bis(trifluoromethanesulfonyl)imidate](triphenylphosphine)gold(I); water In toluene at 90℃; for 3h; Microwave irradiation; Green chemistry; | 99% |
Conditions | Yield |
---|---|
aluminium trichloride at 25℃; for 0.75h; Alkylation; | 95% |
With aluminum (III) chloride at -40 - 20℃; Inert atmosphere; |
Conditions | Yield |
---|---|
With indium(III) chloride; 2-Iodophenol In chlorobenzene for 24h; Reflux; regioselective reaction; | 95% |
1-Bromo-2,4,6-triisopropylbenzene
1,3,5-triisopropyl benzene
Conditions | Yield |
---|---|
With ethanol; cobalt(II) tetrabutylporphyrin; potassium hydroxide at 150℃; for 6h; Inert atmosphere; | 94% |
With tributyl-amine; tetrabutylammonium tetrafluoroborate In acetonitrile at 20℃; for 1.8h; Inert atmosphere; Electrolysis; | 84% |
With potassium phosphate; palladium diacetate In methanol; benzene at 40℃; for 18h; | 100 % Chromat. |
With dimethyl(phenyl)silyllithium In tetrahydrofuran at 30℃; for 1h; Inert atmosphere; | 72 %Spectr. |
With potassium hydride; benzene at 150℃; for 21h; Temperature; Inert atmosphere; Sealed tube; | 38 %Spectr. |
trimethyl(3-methylbut-1-yn-1-yl)silane
1,3,5-triisopropyl benzene
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In neat (no solvent) at 60 - 140℃; for 20h; Green chemistry; regioselective reaction; | 86% |
2,4,6-triisopropylphenylsulfonyl chloride
A
1,3,5-triisopropyl benzene
B
2,4,6-Triisopropylthiophenol
Conditions | Yield |
---|---|
With hydrogenchloride; zinc | A n/a B 85% |
3-methyl-but-1-yne
A
1,3,5-triisopropyl benzene
B
1,2,4-triisopropylbenzene
Conditions | Yield |
---|---|
With 1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene-Fe-N(SiMe3)2,6-diisopropylpheny In benzene-d6 at 20℃; for 2h; | A 80% B 10% |
1-Bromo-2,4,6-triisopropylbenzene
4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane
B
1,3,5-triisopropyl benzene
Conditions | Yield |
---|---|
With triethylamine; bis(dibenzylideneacetone)-palladium(0) In 1,4-dioxane at 100℃; for 6h; | A 72% B n/a |
With copper(l) iodide; iron(III)-acetylacetonate; N,N,N,N,-tetramethylethylenediamine; sodium hydride In tetrahydrofuran; mineral oil at -10℃; Inert atmosphere; | A 64% B n/a |
2,4,6-tribromoiodobenzene
1-Bromo-2,4,6-triisopropylbenzene
A
1,3,5-triisopropyl benzene
B
5'-bromo-2,4,6,2'',4'',6''-hexaisopropyl-1,1:3',1''-terphenyl
Conditions | Yield |
---|---|
Stage #1: 2,4,6-triisopropyl-1-bromobenzene With 1,2-dibrom-methane; magnesium In tetrahydrofuran for 3.5h; Heating; Stage #2: 2,4,6-tribromoiodobenzene In tetrahydrofuran for 5h; Heating; Further stages.; | A 117 g B 54% |
Conditions | Yield |
---|---|
electrolysis; | A n/a B 19.2% |
1,4-bis(1-methylethyl)benzene
A
Isopropylbenzene
B
1,3,5-triisopropyl benzene
C
1,3-diisopropylbenzene
D
1,2,4-triisopropylbenzene
E
1,2-diisopropylbenzene
Conditions | Yield |
---|---|
at 199.99 - 234.99℃; under 36961.4 Torr; Product distribution / selectivity; | A 2.6% B 2.9% C 8.3% D 1.3% E 0.1% |
2,4,6-triisopropyl-benzenesulfonic acid n-hexylester
A
1,3,5-triisopropyl benzene
B
2,4,6-triisopropyl-benzenesulfinic acid
C
hexan-1-ol
Conditions | Yield |
---|---|
With lithium amalgam In 1,4-dioxane at 23℃; for 2h; | A 5% B n/a C 7% |
1,3-diisopropylbenzene
1,2-diisopropylbenzene
A
Isopropylbenzene
B
1,4-bis(1-methylethyl)benzene
C
1,3,5-triisopropyl benzene
D
1,2,4-triisopropylbenzene
Conditions | Yield |
---|---|
at 199.99 - 234.99℃; under 36961.4 Torr; Product distribution / selectivity; | A 1% B 3.3% C 1.2% D 0.4% |
Conditions | Yield |
---|---|
With tetrafluoroboric acid | |
With tetrafluoroboric acid |
Conditions | Yield |
---|---|
With aluminium trichloride at 60℃; | |
With aluminium trichloride at 26.85 - 119.85℃; Equilibrium constant; Thermodynamic data; Isomerization; |
Conditions | Yield |
---|---|
With aluminium trichloride |
1,3,5-tri(2-hydroxyisopropyl)benzene
1,3,5-triisopropyl benzene
Conditions | Yield |
---|---|
With ethanol; copper oxide-chromium oxide at 225℃; under 110326 Torr; Hydrogenation; |
Conditions | Yield |
---|---|
With sulfuric acid at 30 - 40℃; | |
With aluminium trichloride at 60℃; | |
With aluminium trichloride at 70℃; |
Conditions | Yield |
---|---|
With aluminium trichloride at 60℃; unter Stickstoff; | |
With aluminium trichloride at -10℃; Behandeln mit Wasser; |
Conditions | Yield |
---|---|
With methanesulfonic acid at 80 - 100℃; |
Isopropylbenzene
carbon monoxide
A
1,4-bis(1-methylethyl)benzene
B
1,3,5-triisopropyl benzene
C
2,5-di-isopropylbenzaldehyde
D
(4-isopropylbenzaldehyde)
Conditions | Yield |
---|---|
With trifluorormethanesulfonic acid under 76000.1 Torr; for 3h; Ambient temperature; | A 2 % Chromat. B 7 % Chromat. C 31 % Chromat. D 32 % Chromat. |
With trifluorormethanesulfonic acid under 76000.1 Torr; for 3h; Product distribution; Ambient temperature; formylation reaction is in competition with disproportionation; | A 2 % Chromat. B 7 % Chromat. C 31 % Chromat. D 32 % Chromat. |
Isopropylbenzene
A
1,4-bis(1-methylethyl)benzene
B
1,3,5-triisopropyl benzene
C
2,5-di-isopropylbenzaldehyde
D
(4-isopropylbenzaldehyde)
Conditions | Yield |
---|---|
With trifluorormethanesulfonic acid; carbon monoxide under 76000.1 Torr; for 3h; Ambient temperature; | A 2 % Chromat. B 7 % Chromat. C 31 % Chromat. D 32 % Chromat. |
1,4-bis(1-methylethyl)benzene
A
Isopropylbenzene
B
1,3,5-triisopropyl benzene
Conditions | Yield |
---|---|
zeolite (type 13 NaHX) In pentane; benzene at 260.1℃; under 18751.5 - 150012 Torr; Kinetics; Product distribution; catalyst deactiv. and reactiv. in dependence on pressure; |
A
1,3,5-triisopropyl benzene
B
36,51-(epoxy<2,4>hexadiynoxy)-22,26:61,65-dimethano-2,56:19,31-dimetheno-3,55,18,32-(methynoxy<2,4>hexadiynoxymethyno)-1H,20H,28H,30H,57H,59H-bis<1,3>benzodioxocino<9,8-d:9',8'-d'>bis<1,3>benzodioxocino<9',10':19,20;10'',9'':29,30><1,3,6,13,16,18,21,28>
Conditions | Yield |
---|---|
In chloroform-d1 at 25℃; Rate constant; |
propene
benzene
A
Isopropylbenzene
B
1,4-bis(1-methylethyl)benzene
C
1,3,5-triisopropyl benzene
D
1,3-diisopropylbenzene
E
1,2,4-triisopropylbenzene
F
1,2-diisopropylbenzene
Conditions | Yield |
---|---|
aluminosilicate (15percent Al2O3) at 40℃; Product distribution; other catalysts (Ga, In, Mg, La silicates); | A 17.5 % Chromat. B 1.9 % Chromat. C 0.2 % Chromat. D n/a E 0.9 % Chromat. F n/a |
propene
benzene
A
Isopropylbenzene
B
1,4-bis(1-methylethyl)benzene
C
1,3,5-triisopropyl benzene
D
1,3-diisopropylbenzene
E
1,2-diisopropylbenzene
Conditions | Yield |
---|---|
aluminosilicate at 70℃; Rate constant; Product distribution; effect of the composition and amount of catalysts, reaction time and temperature; | |
zeolite beta CP 786 catalyst at 132 - 133℃; under 15757.7 - 15809.5 Torr; Product distribution / selectivity; |
propene
benzene
A
Isopropylbenzene
B
1,4-bis(1-methylethyl)benzene
C
1,3,5-triisopropyl benzene
D
1,2,4-triisopropylbenzene
E
1,2-diisopropylbenzene
F
tris-(isopropyl)benzene
Conditions | Yield |
---|---|
aluminosilicates at 39.9℃; under 75006 Torr; Product distribution; temperature, volume flow rate, molar ratio, nature of the catalyst; |
propene
benzene
A
Isopropylbenzene
B
1,4-bis(1-methylethyl)benzene
C
1,3,5-triisopropyl benzene
D
1,2-diisopropylbenzene
Conditions | Yield |
---|---|
at 313℃; under 75006 Torr; Further byproducts given. Title compound not separated from byproducts; |
1,3,5-triisopropyl benzene
Conditions | Yield |
---|---|
With trifluorormethanesulfonic acid In dichloromethane at 20℃; for 24h; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
With [bis(acetoxy)iodo]benzene; iodine In ethyl acetate at 60℃; for 16h; | 99% |
With [bis(acetoxy)iodo]benzene; iodine In ethyl acetate at 60℃; for 16h; Iodination; | 99% |
With iodine; 1-(p-methylbenzenesulfonyloxy)-1,2-benziodoxol-3(1H)-one In 1,2-dichloro-ethane for 16h; Ambient temperature; | 98% |
Conditions | Yield |
---|---|
With 1,1,1,3',3',3'-hexafluoro-propanol at 25℃; for 2h; | 98% |
trans-chrotonyl chloride
1,3,5-triisopropyl benzene
(E)-1-(2,4,6-triisopropylphenyl)-2-buten-1-one
Conditions | Yield |
---|---|
With aluminium trichloride In carbon disulfide Heating; | 95% |
fluorobenzene
1,3,5-triisopropyl benzene
chlorodicyclohexylphosphane
XPhos
Conditions | Yield |
---|---|
Stage #1: fluorobenzene With lithium diisopropyl amide In tetrahydrofuran at -78℃; for 2h; Inert atmosphere; Stage #2: chlorodicyclohexylphosphane In tetrahydrofuran at 15℃; for 10h; Stage #3: 1,3,5-triisopropyl benzene With n-butyllithium; potassium tert-butylate In hexane at 30 - 60℃; for 16h; Reagent/catalyst; Temperature; | 93% |
Conditions | Yield |
---|---|
With chlorosulfonic acid In chloroform at 0℃; | 92% |
With chlorosulfonic acid In chloroform 1.) 0 deg C, 30 min, 2.) 1 h, room temp.; | 85% |
With chlorosulfonic acid; sodium chloride In tetrachloromethane; hexane; chloroform at 0℃; | 65% |
1,3,5-triisopropyl benzene
1-chloro-2,4,6-tri(iso-propyl)benzene
Conditions | Yield |
---|---|
With chloro-trimethyl-silane; bis-[(trifluoroacetoxy)iodo]benzene In dichloromethane at 20℃; for 18h; Reagent/catalyst; Inert atmosphere; | 92% |
With 1-(p-methylbenzenesulfonyloxy)-1,2-benziodoxol-3(1H)-one; lithium chloride In acetonitrile for 18h; Ambient temperature; | 84% |
With 1-(p-toluenebenzenesulfonyloxy)-1,2-benziodoxol-3(1H)-on; lithium chloride In acetonitrile for 16h; Product distribution; Ambient temperature; other reagents (trivalent iodine compounds + LiCl or Bu4NCl); | 84% |
With 1-(p-methylbenzenesulfonyloxy)-1,2-benziodoxol-3(1H)-one; lithium chloride In acetonitrile for 16h; Ambient temperature; | 84% |
With N-chloro-succinimide; triphenylphosphine sulfide In chloroform-d1 at 20℃; for 3h; | 57 %Spectr. |
3-thienyl iodide
1,3,5-triisopropyl benzene
Conditions | Yield |
---|---|
Stage #1: 3-thienyl iodide; 1,3,5-triisopropyl benzene With 3-chloro-benzenecarboperoxoic acid In dichloromethane at 20℃; for 2h; Stage #2: tetrafluoroboric acid In dichloromethane at 0 - 20℃; for 2h; | 89% |
Conditions | Yield |
---|---|
With triethylamine In water | 88% |
1,3,5-triisopropyl benzene
Conditions | Yield |
---|---|
With trifluorormethanesulfonic acid In dichloromethane at 40℃; for 36h; Schlenk technique; Inert atmosphere; | 87% |
1,3,5-triisopropyl benzene
Dichloromethyl methyl ether
2,4,6-triisopropylbenzaldehyde
Conditions | Yield |
---|---|
With titanium tetrachloride In dichloromethane for 12h; | 86% |
With titanium tetrachloride In dichloromethane Ambient temperature; | 80% |
With silver trifluoromethanesulfonate In dichloromethane at -78℃; for 0.333333h; Inert atmosphere; | 72% |
With titanium tetrachloride Multistep reaction; | |
With titanium tetrachloride Inert atmosphere; |
trifluorormethanesulfonic acid
1,3,5-triisopropyl benzene
[bis(acetoxy)iodo]benzene
phenyl(2,4,6-triisopropylphenyl)iodonium trifluoromethanesulfonate
Conditions | Yield |
---|---|
In dichloromethane at 0 - 20℃; for 2h; | 86% |
Conditions | Yield |
---|---|
Stage #1: trifluorormethanesulfonic acid; pentafluoro(2-iodophenyl)-λ6-sulfane With 3-chloro-benzenecarboperoxoic acid In dichloromethane at 0 - 20℃; for 2h; Inert atmosphere; Stage #2: 1,3,5-triisopropyl benzene In dichloromethane at 0 - 20℃; for 18h; Inert atmosphere; | 86% |
1,3,5-triisopropyl benzene
3-Methylbenzoyl chloride
m-Tolyl-(2,4,6-triisopropyl-phenyl)-methanone
Conditions | Yield |
---|---|
With aluminium trichloride In carbon disulfide for 12h; Ambient temperature; | 85% |
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