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:105-05-5
Min.Order:1 Metric Ton
Negotiable
Type:Manufacturers
inquiryThe 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
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
Cas:105-05-5
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Lab/Research institutions
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
Cas:105-05-5
Min.Order:5 Kiloliter
FOB Price: $1.2 / 5.0
Type:Manufacturers
inquiryMethanesulfonic acid is a raw material for medicine and pesticide. It can also be used as dehydrating agent, curing accelerator for coating, treating agent for fiber, solvent, catalysis, and esterification as well as polymerization reaction. It c
Cas:105-05-5
Min.Order:1 Kilogram
FOB Price: $4.0 / 5.0
Type:Trading Company
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
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:105-05-5
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
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:105-05-5
Min.Order:10 Gram
FOB Price: $100.0
Type:Lab/Research institutions
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 Intermediat
Appearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
Triumph has the complete production of G- KG - MT service chain,we can make the new technology into productivity quickly in the research and development of new products. Main Business Custom Synthesis:
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
R & D enterprises have their own stock in stock Package:1kg Application:pharmaceutical intermediates
1.High quality : the purity is 99% min . through multiple producing procedures. 2.Competitive price : low price because of our skilled production technolpgy ,save the production cost at most , and give big profit room to our customers702.Safe and fa
high quality Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea
Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
1.Our services:A.Supply sampleB.The packing also can be according the customers` requirmentC.Any inquiries will be replied within 24 hoursD.we provide Commerical Invoice, Packing List, Bill of loading, COA , Health certificate and Origin certificate.
Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:105-05-5
Min.Order:1 Kilogram
FOB Price: $112.0
Type:Trading Company
inquiryAnsciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
Amoychem is committed to providing the top-quality chemical products and services Internationally. We offer our customers with friendly, professional service and reliable, high performance products that have been manufactured according to the accredi
1,4-Diethylbenzene CAS NO.105-05-5 Application:1,4-Diethylbenzene CAS NO.105-05-5
1,we produce and sell good chemicals around the world. 2,our success rate is about 95%. this means, if customer order is accepted, the probability that the customer will obtain the ordered substances, is 95%. 3,our staff consists of highl
1,4-Diethylbenzene CAS NO.105-05-5Appearance:off-white fine crystalline powder Storage:Dry and ventilated Package:Standard or as customer's require Application:intermediates Transportation:By express (Door to door) such as FEDEX, DHL, EMS for small a
Cas:105-05-5
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:any port in China
Our mission is to provide high-quality and innovative products to our customers. By offering a broad range of products, custom synthesis and personalized services, Bide can help scientists speeding up their research in the chemical and pharmaceutical
1.Professional synthesis laboratory and production base. 2.Strong synthesis team and service team. 3.Professional data management system. 4.We provide the professional test date and product information ,ex. HNMR ,CNMR,FNMR, HPLC/G
Cas:105-05-5
Min.Order:10 Milligram
Negotiable
Type:Lab/Research institutions
inquiry1,4-DIETHYLBENZENE Basic information Product Name: 1,4-DIETHYLBENZENE
Cas:105-05-5
Min.Order:100 Gram
Negotiable
Type:Trading Company
inquiryChangzhou Extraordinary Pharmatech co., LTD. As a leading chemical manufacturer and supplier in China.DAS authentication is passed.We can provide the popular precursor chemicals, we have our own strong R & D team, have our own laboratories and fa
Conditions | Yield |
---|---|
With triethylsilane; indium(III) bromide In chloroform at 60℃; for 1h; Inert atmosphere; | 99% |
With hydrogen; palladium on activated charcoal In methanol at 20℃; for 24h; | 72% |
With hydrogen In 1,3,5-trimethyl-benzene at 175℃; under 37503.8 Torr; for 16h; Autoclave; |
Conditions | Yield |
---|---|
With zeolite H-beta In tetrahydrofuran at 249.84℃; under 20686.5 Torr; for 18h; Reagent/catalyst; | 99% |
1,4-diethylbenzene
Conditions | Yield |
---|---|
With chlorosulfonic acid In dichloromethane at 0℃; regioselective reaction; | 85% |
With lead(IV) tetraacetate; lithium chloride In chloroform for 3h; Reflux; |
Conditions | Yield |
---|---|
With hydrogenchloride; hydrogen; palladium on activated charcoal In ethanol at 50℃; under 3102.97 Torr; | 77% |
With hydrogenchloride; amalgamated zinc | |
With nickel at 260 - 280℃; durch Hydrogenolyse; |
methanol
dispiro<2.2.2.2>deca-4,9-diene
A
1,4-diethylbenzene
B
1-Ethyl-4-(2-methoxyethyl)benzol
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal | A n/a B 50% |
trifluoromethanesulfonic acid ethyl ester
benzene
A
ethylbenzene
B
1,4-diethylbenzene
C
ortho-diethylbenzene
Conditions | Yield |
---|---|
for 2h; Heating; Yields of byproduct given; | A 30% B n/a C n/a |
for 2h; Heating; Yield given; | A 30% B n/a C n/a |
4-methyl-4-phenylcyclohex-2-enone
A
1-Methyl-3-ethylbenzene
B
2-Ethyltoluene
C
m-diethylbenzene
D
1,4-diethylbenzene
E
ortho-diethylbenzene
F
3-ethyl-o-xylene
Conditions | Yield |
---|---|
With chloranil Product distribution; 1.) 510 deg C, 12 Torr; 2.) benzene, reflux, 20 h; other conditions investigated; | A 1.2% B 0.2% C 1.5% D 1.3% E 10% F 19% |
Conditions | Yield |
---|---|
With mesoporous graphitic C3N4 at 150℃; for 24h; Friedel-Crafts reaction; | 18% |
Conditions | Yield |
---|---|
With [NiNPtBu3]4; phenylsilane In tetrahydrofuran at 60℃; for 16h; Sealed tube; | A 10% B 16% C n/a |
4-methyl-4-phenylcyclohex-2-enone
A
o-xylene
B
1-Methyl-3-ethylbenzene
C
2-Ethyltoluene
D
ethylbenzene
E
m-diethylbenzene
F
1,4-diethylbenzene
Conditions | Yield |
---|---|
With chloranil Product distribution; 1.) 510 deg C, 12 Torr; 2.) benzene, reflux, 20 h; other conditions investigated; | A 0.5% B 1.2% C 0.2% D 12% E 1.5% F 1.3% |
ethanol
ethylbenzene
A
m-diethylbenzene
B
1,4-diethylbenzene
C
ortho-diethylbenzene
Conditions | Yield |
---|---|
HZSM-5 type zeolite modified with 10 wtpercent oxide of boron at 399.9℃; Yield given. Yields of byproduct given; | |
With MgMnAPO-5 at 250℃; Product distribution; Further Variations:; Temperatures; Reagents; atmospheric pressure; | A 0.22% B 0.52% C 0.05% |
With hydrogen at 380℃; under 760.051 Torr; for 4h; Flow reactor; |
Conditions | Yield |
---|---|
With sodium |
Conditions | Yield |
---|---|
at 24℃; under 72079.8 Torr; Leiten ueber ein Gemisch von Difluorophosphorsaeure und Borfluorid; |
Conditions | Yield |
---|---|
With aluminium trichloride |
Conditions | Yield |
---|---|
With sodium |
Conditions | Yield |
---|---|
With aluminium trichloride Trennung durch Darstellung der Sulfonsaeuren; |
Conditions | Yield |
---|---|
With aluminium trichloride durch Behandeln mit rauchender Schwefelsaeure; |
Conditions | Yield |
---|---|
With aluminium trichloride at 70℃; | |
With catalyst beds at 370 - 400℃; under 5250.53 Torr; |
Conditions | Yield |
---|---|
With As-HZSM-5 zeolite at 399.9℃; under 304 Torr; Product distribution; other zeolites; | |
With As-HZSM-5 zeolite at 399.9℃; under 304 Torr; Yield given; | |
Ga-Al-ZSM-5 derived catalysts A-F at 330℃; Product distribution / selectivity; Gas phase; | |
With B2O3/ZSM-5 at 359.84℃; for 6h; Inert atmosphere; Flow reactor; |
ethanol
ethylbenzene
A
m-diethylbenzene
B
1,4-diethylbenzene
C
ortho-diethylbenzene
D
toluene
E
benzene
Conditions | Yield |
---|---|
HZSM-5 type zeolite at 399.9℃; Product distribution; modified catalysts; p-selectivity in diethylbenzene; | |
With hydrogen at 380℃; under 760.051 Torr; for 4h; |
ethanol
A
1-Methyl-3-ethylbenzene
B
para-xylene
C
ethylbenzene
D
4-methylethylbenzene
E
1,4-diethylbenzene
F
toluene
Conditions | Yield |
---|---|
ZSM-5-2 In gaseous matrix at 339.9℃; under 760 Torr; Product distribution; contact time 0.25 s; with ZSM-5-1 and SilAl2; other temperature; shape effects in the conversion; |
ethene
ethylbenzene
A
m-diethylbenzene
B
1,4-diethylbenzene
C
ortho-diethylbenzene
Conditions | Yield |
---|---|
H-ZSM-5 catalyst at 400℃; Product distribution; alkylation of benzene and momosubstituted benzenes with ethylene over H-ZSM-5 and mordenite-H catalysts; isomerization of ethylarenes over H-mordenite; |
ethylbenzene
A
1-Methyl-3-ethylbenzene
B
4-methylethylbenzene
C
m-diethylbenzene
D
1,4-diethylbenzene
E
ortho-diethylbenzene
F
benzene
Conditions | Yield |
---|---|
With hydrogen; HTsVM zeolite at 400℃; under 11250.9 Torr; Product distribution; var. catalyst; |
ethylbenzene
A
m-diethylbenzene
B
1,4-diethylbenzene
C
ortho-diethylbenzene
D
benzene
Conditions | Yield |
---|---|
With trifluorormethanesulfonic acid at 25℃; Product distribution; var. time, effect of add. mesitylene and 1,3,5-triethylbenzene; | |
zeolite SSZ-53 Product distribution; Further Variations:; Temperatures; atmospheric pressure; |
dispiro<2.2.2.2>deca-4,9-diene
A
trans-1,4-Diethylcyclohexan
B
cis-1,4-Diethylcyclohexan
C
1,4-diethylbenzene
D
6-Ethylspiro<2.5>octan
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In ethyl acetate Ambient temperature; Yield given. Yields of byproduct given; | |
With hydrogen; palladium on activated charcoal In ethyl acetate Product distribution; Mechanism; Ambient temperature; further catalysts; further solvents; | |
With hydrogen; palladium on activated charcoal In 2,2,4-trimethylpentane at 25℃; Thermodynamic data; ΔHH; |
dispiro<2.2.2.2>deca-4,9-diene
A
cis-1,4-Diethylcyclohexan
B
1,4-diethylbenzene
C
Dispiro<2.2.2.2>decan
D
6-Ethylspiro<2.5>octan
Conditions | Yield |
---|---|
With hydrogen; platinum on activated charcoal In ethyl acetate Yield given. Further byproducts given. Yields of byproduct given; |
ethanol
toluene
A
1-Methyl-3-ethylbenzene
B
2-Ethyltoluene
C
4-methylethylbenzene
D
m-diethylbenzene
E
1,4-diethylbenzene
F
ortho-diethylbenzene
Conditions | Yield |
---|---|
With zeolit derivatives Product distribution; various zeolit products, various mol ratio, and temperature; |
ethene
toluene
A
1-Methyl-3-ethylbenzene
B
4-methylethylbenzene
C
1,4-diethylbenzene
D
1-ethyl-2,4-dimethyl-benzene
Conditions | Yield |
---|---|
With phosphorus-modified zeolite-ZSM-5 at 320℃; Further byproducts given. Title compound not separated from byproducts; | A 26.97 % Chromat. B 13.77 % Chromat. C 0.7 % Chromat. D 0.91 % Chromat. |
para-xylene
dimethyl sulfate
A
4-methylethylbenzene
B
1,4-diethylbenzene
Conditions | Yield |
---|---|
With n-butyllithium; potassium tert-butylate 1.) hexane, reflux, 1 h; Yield given. Multistep reaction. Yields of byproduct given; |
ethene
benzene
A
Isopropylbenzene
B
tert-butylbenzene
C
ethylbenzene
D
1,4-diethylbenzene
E
toluene
Conditions | Yield |
---|---|
superhigh-silica zeolites H form Rate constant; Product distribution; Mechanism; study of catalytic properties of catalysts containing 20 percent H-SHSZ and 80 percent γ-alumina; effect of components used at catalyst synthesis on the catalytic activity; various reaction conditions; |
1,4-diethylbenzene
diethyl methylthio(chloro)methanephosphonate
[(2,5-Diethyl-phenyl)-methylsulfanyl-methyl]-phosphonic acid diethyl ester
Conditions | Yield |
---|---|
With tin(IV) chloride In dichloromethane for 0.666667h; Ambient temperature; | 99% |
1,4-diethylbenzene
1,4-diethyl-2,5-diiodobenzene
Conditions | Yield |
---|---|
With sulfuric acid; iodine; periodic acid In water; acetic acid at 95℃; for 24h; | 99% |
With sulfuric acid; iodine; periodic acid In water; acetic acid at 100℃; for 22h; | 56% |
Cu(OCH(C6H5)2)(P(C6H5)3)3
1,4-diethylbenzene
Conditions | Yield |
---|---|
In diethyl ether inert atmosphere; room temp.; stirring; 2 h;; ppt. washed with hexane; elem. anal.;; | 96% |
Conditions | Yield |
---|---|
With aluminum (III) chloride; nitromethane at 19 - 22℃; under 760.051 Torr; Friedel Crafts acylation; Inert atmosphere; | 94% |
With aluminium trichloride In nitromethane for 5h; Ambient temperature; |
1,4-diethylbenzene
2,5-diethylbenzene-1-sulfonyl chloride
Conditions | Yield |
---|---|
With chlorosulfonic acid In dichloromethane; benzene | 94% |
Conditions | Yield |
---|---|
With Iron(III) nitrate nonahydrate; N-hydroxyphthalimide; acetic acid at 110℃; for 10h; | 91% |
With chromium(VI) oxide; Ce(2+)*2O4S(2-) In acetic acid at 5 - 50℃; for 5h; | 89% |
With FeH6Mo6O24(3-)*3H3N*3H(1+)*7H2O; tetrabutylammomium bromide; dihydrogen peroxide In 1,4-dioxane at 70℃; for 24h; | 83% |
Conditions | Yield |
---|---|
In bromine | A n/a B 90% |
1,4-diethylbenzene
2,5-diethyl-bromobenzene
Conditions | Yield |
---|---|
With bromine; iron at 20℃; Cooling with ice; | 90% |
1,4-diethylbenzene
1,4-diethyl-2-iodobenzene
Conditions | Yield |
---|---|
With sulfuric acid; potassium 4-iodylbenzene-1-sulfonate; iodine In water; acetonitrile at 65℃; for 12h; | 89% |
With sulfuric acid; iodine; acetic acid; periodic acid In water at 95℃; for 0.416667h; Inert atmosphere; | 82% |
1,4-diethylbenzene
2-(4-methoxyphenylamino)acetic acid methyl ester
Conditions | Yield |
---|---|
Stage #1: 1,4-diethylbenzene With 2,3-dicyano-5,6-dichloro-p-benzoquinone; copper dichloride at 90℃; for 2h; Stage #2: 2-(4-methoxyphenylamino)acetic acid methyl ester With oxygen at 20 - 60℃; regioselective reaction; | 88% |
1,4-diethylbenzene
1,2,4,5-tetrabromo-3,6-diethylbenzene
Conditions | Yield |
---|---|
With bromine; iron at 0 - 6℃; | 87% |
With aluminum tri-bromide; bromine | |
With beryllium; diethyl ether; bromine |
1,4-diethylbenzene
toluene-4-sulfonamide
N-(α-methyl-4-ethylbenzyl)-p-toluenesulfonamide
Conditions | Yield |
---|---|
With tetrabutylammonium tetrafluoroborate In 1,2-dichloro-ethane at 20℃; for 2.5h; Electrochemical reaction; Inert atmosphere; regioselective reaction; | 82% |
With 1,3-Diiodo-5,5-dimethyl-2,4-imidazolidinedione In tetrachloromethane at 60℃; for 24h; Inert atmosphere; Darkness; | 79% |
1,4-diethylbenzene
Conditions | Yield |
---|---|
With Cu(2,9-bis(panisyl)-1,10-phenanthroline)2Cl; 1-azido-1λ3-benzo[d][1,2]iodaoxol-3(1H)-one In acetonitrile at 20℃; for 16h; Sealed tube; Inert atmosphere; Irradiation; | 82% |
Conditions | Yield |
---|---|
With dihydrogen peroxide; cobalt(II) diacetate tetrahydrate; potassium bromide In acetic acid at 80℃; for 6h; Reagent/catalyst; Solvent; Temperature; | 80% |
With FeH6Mo6O24(3-)*3H3N*3H(1+)*7H2O; tetrabutylammomium bromide; dihydrogen peroxide In 1,4-dioxane at 70℃; for 24h; | 76% |
With tert.-butylnitrite; N-hydroxyphthalimide In acetonitrile at 80℃; for 24h; Schlenk technique; | 71% |
Conditions | Yield |
---|---|
With ruthenium trichloride; iodobenzene; potassium peroxymonosulfate In water; acetonitrile at 20℃; for 3h; Inert atmosphere; | A 77% B 11% |
With Oxone In water; acetonitrile at 20℃; for 12h; | A 77% B 15% |
With tert.-butylhydroperoxide; 1-n-butyl-3-methylimidazolim bromide In water at 20℃; for 12h; | A 44% B 22% |
With ruthenium trichloride; iodobenzene; potassium peroxomonosulfate In water; acetonitrile at 20℃; for 3h; | |
With tert.-butylnitrite; N-hydroxyphthalimide; oxygen In acetonitrile at 80℃; under 760.051 Torr; for 24h; Schlenk technique; | A 62 %Spectr. B 12 %Spectr. |
Conditions | Yield |
---|---|
With trifluorormethanesulfonic acid In nitromethane Schlenk technique; Reflux; regioselective reaction; | 77% |
Conditions | Yield |
---|---|
With europium(III) bis(trifluoromethylsulfonyl)imide at 250℃; for 12h; Friedel-Crafts acylation; | 74% |
4,4,5,5-pentamethyl-2-(1'-n-butyl-pyrazole-4'-yl)-4,5-dihydro-1H-imidazolyl-3-oxide-1-oxyl
1,4-diethylbenzene
Conditions | Yield |
---|---|
In further solvent(s) dissolving mixt. of copper compd. and nitronyl nitroxide deriv. in 1,4-diethylbenzene with heating to 70°C for 2-3 min; cooling to room temp., keeping with slow evapn. at 5°C for 1-2 d,filtration, washing with cold heptane, air drying, elem. anal.; | 71% |
Conditions | Yield |
---|---|
With 2,2'-isopropylidenebis[(4S)-4-tert-butyl-2-oxazoline]; N-fluorobis(benzenesulfon)imide; copper(l) chloride In acetonitrile at 60℃; for 24h; Reagent/catalyst; Glovebox; Inert atmosphere; Sealed tube; | 69% |
1,4-diethylbenzene
1-(4-methyl-benzenesulfonyl)-benzimidazole
Conditions | Yield |
---|---|
With N-chloro-succinimide; copper(I) trifluoromethanesolfonate toluene complex; iron(III) perchlorate hydrate; 3,4,7,8-Tetramethyl-o-phenanthrolin; di-tert-butyl peroxide; lithium carbonate; lithium bromide In toluene at 120℃; for 36h; Schlenk technique; Inert atmosphere; Molecular sieve; | 69% |
Conditions | Yield |
---|---|
With 2,2'-isopropylidenebis[(4S)-4-tert-butyl-2-oxazoline]; N-fluorobis(benzenesulfon)imide; copper(l) chloride In acetonitrile at 60℃; for 24h; Glovebox; Inert atmosphere; Sealed tube; | 64% |
morpholine
1,4-diethylbenzene
1-(4-ethylphenyl)-2-(morpholin-4-yl)ethane-1,2-dione
Conditions | Yield |
---|---|
With tert.-butylhydroperoxide; copper(l) iodide In neat (no solvent) at 50℃; for 24h; | 62% |
1,4-diethylbenzene
A
4-ethylacetophenone
B
1,4-Diacetylbenzene
C
1-(4-ethylphenyl)ethanol
Conditions | Yield |
---|---|
With cerium(IV) triflate; water at 20℃; for 25h; | A 61.3% B 33.3% C 3.6% |
1,4-diethylbenzene
1,4-dibromo-2,5-diethylbenzene
Conditions | Yield |
---|---|
With bromine; iodine at 0 - 20℃; for 2h; | 60% |
With bromine; iodine at 0 - 20℃; for 24h; Darkness; | 60% |
Conditions | Yield |
---|---|
With trifluoroacetic acid Heating; | 54% |
1,4-diethylbenzene
N,N-dimethyl-formamide
2-(4-ethylphenyl)-N,N-dimethyl-2-oxoacetamide
Conditions | Yield |
---|---|
With tert.-butylhydroperoxide; tetra-(n-butyl)ammonium iodide at 80℃; for 18h; Sealed tube; | 54% |
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