High quality products. Always supply highest grade to you. Purity:≥99.5% Reasonable & Competitive Price. Huge capacity determines the lowest shared cost. The more you buy the more competitive prices you will get. The sincerest and most p
Cas:79-10-7
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inquiryDayangChem exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product spe
Cas:79-10-7
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inquiryItems Standard Result Purity 99.5%MIN 99.6% Water Content 0.2%MAX 0.06%
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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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inquiryClassification: Chemical Auxiliary Agent CAS No.: 79-10-7 Other Names: AA; Acroleic Acid MF: C3H4O2 EINECS No.: 201-177-9 Purity: 99.5% min Place of Origin: Anhui, China (Mainland) Type: Carbon Black Usage: Pa
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
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, intermedi
Product Name: Acrylic acid Synonyms: ETHYLENECARBOXYLIC ACID;2-PROPENOIC ACID;AKOS BBS-00003787;ACRYLIC ACID;Acroleic acid;RARECHEM AL BO 0141;PROPENOIC ACID;2-Propensαure CAS: 7
Our 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
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inquiryProduct Detail Minimum Order Qty. 10 Gram
Cas:79-10-7
Min.Order:10 Gram
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inquiryHebei Mojin Biotechnology Co., Ltd, Our company is a professional in lead acetate, diphenyl ethylamine and other chemical raw materials and chemical reagents research and development production enterprises. Our business covers more than 30 countrie
Cas:79-10-7
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inquiryProduct Name: Acrylic acid Synonyms: Racecadotril Impurity N;acrylic acid E:candyli(at)speedgainpharma(dot)com;AKOS BBS-00003787;ACRYLIC ACID;Acroleic acid;RARECHEM AL BO 0141;PROPENOIC ACID;2-Propensαure CAS: 79-10-7 MF: C3H4O2 MW:
Cas:79-10-7
Min.Order:1 Kilogram
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inquiryAcrylicacid CAS:79-10-7 Specification Items Specification Appearance Clear Colourless liquid, Odour Pungent smess Purity ≥ 99.5% Colour, Hazen
Cas:79-10-7
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inquiryAppearance:colorless liquid Storage:Store in a cool,dry place and keep away from direct strong light Package:As customer request Application:Used for research and industrial manufacture. Transportation:Common products:Sea/Air/Co
Our Services 1. New Molecules R&D 2. Own test center HPLC NMR GC LC-MS 3. API and Intermediates from China reputed manufacturers 4. Documents support COA MOA MSDS DMF open part Our advantages 1. Government awarded company. Top 100 enter
Cas:79-10-7
Min.Order:1 Gram
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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
Massive Chemical is certified with ISO9001 and ISO14001 manufacturer for this product. We will offer all documents as requirement for the materials which includes, Certificate of Analysis, Material Safety Data Sheet, and Method of Analysis and
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:79-10-7
Min.Order:10 Gram
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Type:Lab/Research institutions
inquirySuperior quality, moderate price & quick delivery. Appearance:colorless liquid Storage:Store in a cool, ventilated warehouse.The storage temperature should not exceed 5 ° C ,and the inside humidity preferably not more than 85%. Package:200kg/ba
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:79-10-7
Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiryOur clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
Hunan chemfish Pharmaceutical co.,Ltd.located in Lugu High-tech industral park ,Hunan province . with its own R&D center and more than 10000㎡manufacture plant . Chemfish owns 40 reactors from 1000L to 8000L. With complete auxiliary equipment as
Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:79-10-7
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
high 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
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,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
Acrylic acid Application:Acrylic acid and acrylate can be uniformly polymerized and copolymerized, and their polymers are used in synthetic resin, synthetic fiber, high water absorbent resin, building materials, coatings and Transportation:By express
Conditions | Yield |
---|---|
With N-hydroxyphthalimide; trans-Re(O)Cl2(OC(CH3)2C(CH3)2O)2P(Ph)3; oxygen In acetonitrile at 30℃; under 760.051 Torr; for 7h; | 100% |
With dihydrogen peroxide In acetonitrile at 70℃; for 3h; Reagent/catalyst; | 100% |
With C4H11FeMo6NO24(3-)*3C16H36N(1+); water; oxygen; sodium carbonate at 50℃; under 760.051 Torr; for 8h; Green chemistry; | 98% |
Conditions | Yield |
---|---|
titanium catalyst 16-30 mesh at 180 - 190℃; for 45h; Product distribution / selectivity; | 100% |
With 4-methoxy-phenol; silica gel at 250℃; Gas phase; | 97% |
sulfuric acid at 160℃; Product distribution / selectivity; | 96.2% |
Conditions | Yield |
---|---|
With water; sodium hydroxide In hexan-1-ol at 80℃; for 10h; Temperature; Sealed tube; | 99.9% |
With potassium carbonate | |
With lead(II) oxide Destillation; |
Conditions | Yield |
---|---|
With water at 0 - 4℃; for 7.5h; culture broth containing cells of Pseudomonas chlororaphis, strain B23; | A 99% B 0.7% |
With water; copper oxide, reduced, supported in stainless steel wire socks at 135 - 158℃; under 3760.13 Torr; Heating / reflux; |
Conditions | Yield |
---|---|
With potassium phosphate buffer at 30℃; for 0.5h; Rhodococcus sp. AJ270 cells; | 98.1% |
With potassium phosphate buffer; nitrilase from Alcaligenes faecalis ATCC8750 at 30℃; for 9h; pH=7.3; | 93% |
With sulfuric acid; copper; hydroquinone | |
With bradyrhizobium species BTAi1 (A5EKU8); water Reagent/catalyst; Enzymatic reaction; | |
With water In aq. phosphate buffer at 37℃; pH=7; Green chemistry; Enzymatic reaction; |
Conditions | Yield |
---|---|
In pyridine; ethyl acetate; benzene | 97.8% |
Conditions | Yield |
---|---|
C150Cu2Mo12Nb2SbSi150V3.5 In nitrogen; water at 280℃; | 97.6% |
Conditions | Yield |
---|---|
With hydrogen In methanol at 20℃; under 760.051 Torr; for 5h; Green chemistry; | 97% |
With hydrogen In methanol under 760.051 Torr; for 5.5h; | 94% |
With ethanol; colloid; palladium Hydrogenation; | |
With hydrogen In hexane at 40℃; under 750.075 Torr; for 12h; Catalytic behavior; |
Conditions | Yield |
---|---|
94.1% | |
With carboxylesterase; Tris buffer In ethanol at 27℃; for 0.333333h; Enzyme kinetics; Hydrolysis; Enzymatic reaction; |
Conditions | Yield |
---|---|
With oxygen; catalyst prepared according to U.S. Pat. No. 6,858,561 Product distribution / selectivity; | A 94% B n/a C n/a |
With oxygen; triethyl phosphate at 404 - 419℃; under 2475.25 - 3900.39 Torr; Product distribution / selectivity; | A 54.1% B n/a C n/a |
With oxygen; vanadia at 459.9℃; for 27h; Product distribution; various VPO catalysts in vapor phase, at various times; | A 13.5% B 0.14% C 0.04% |
propene
acrylic acid
Conditions | Yield |
---|---|
With oxygen; B0.4Bi5Co2Fe0.4K0.1Mo12Na0.2Ni3O(x)Si24 at 331 - 410℃; Conversion of starting material; Gas phase; | 92% |
With oxygen; Cu9Mo35Nb3Ni43O(x)Sb100Si20V7 at 300 - 330℃; Conversion of starting material; Gas phase; | 90.5% |
Stage #1: propene With water; oxygen; catalyst with atomic ratio Mo12Bi1.2Fe1.1Co3K0.05W2 at 320℃; Stage #2: With oxygen; catalyst with atomic ratio Mo12V5W1.2Cu2 on α-alumina carrier at 265℃; Product distribution / selectivity; | 90% |
trimethyleneglycol
A
acetaldehyde
B
acetic acid
C
acrylic acid
D
acrolein
Conditions | Yield |
---|---|
With water; oxygen at 269.84℃; under 148.515 Torr; for 0.00391667h; | A n/a B 9% C 91% D n/a |
Conditions | Yield |
---|---|
With water; oxygen; composite oxide containing Mo,Bi,Ni,Co,Fe,Na,B,K,Si from Comparative Example 1 at 315℃; under 760.051 Torr; for 0.000555556h; Conversion of starting material; | A 2.9% B 90.5% |
With water; oxygen; composite oxide containing Mo,Bi,Ni,Co,Fe,Na,B,K,Si from Example 1 at 315℃; under 760.051 Torr; for 0.000555556h; Conversion of starting material; | A 4.2% B 90.1% |
With water; oxygen; composite oxide containing Mo,Bi,Ni,Co,Fe,Na,B,K,Si from Comparative Example 2 at 315℃; under 760.051 Torr; for 0.000555556h; Conversion of starting material; | A 3.8% B 89% |
Conditions | Yield |
---|---|
With potassium phosphate; carbon dioxide; CrH6Mo6O24(3-)*3H3N*3H(1+) In dimethyl sulfoxide at 80℃; under 750.075 Torr; for 24h; Green chemistry; | 90% |
With ammonium cerium (IV) nitrate In water at 65 - 70℃; for 5h; | 84% |
With tert.-butylhydroperoxide; copper(l) chloride In decane; acetonitrile at 20℃; for 4h; | 75% |
Conditions | Yield |
---|---|
With air stream; silicate at 250 - 370℃; for 1h; N2 stream; | 90% |
Conditions | Yield |
---|---|
at 180℃; under 760.051 Torr; | 90% |
LACTIC ACID
acrylic acid
Conditions | Yield |
---|---|
With silica gel In water at 400℃; under 9639.89 Torr; Reagent/catalyst; Temperature; Pressure; Inert atmosphere; | 89.4% |
With potassium metaphosphate; barium diphosphate; O13P4(6-)*3Ba(2+) In water at 350℃; for 3.7h; Catalytic behavior; Time; Reagent/catalyst; Concentration; Temperature; | 85% |
With calcium sulfate; sodium sulfate at 400℃; mit Wasserdampf; |
Conditions | Yield |
---|---|
With precursor catalyst 13 wt percent KPO3, 37 wt percent Ba2P2O7, 50 percent fused silica In water for 72h; Inert atmosphere; Heating; High pressure; Gas phase; | 88% |
With dipotassium hydrogenphosphate; barium(II) nitrate; phosphoric acid In water at 375 - 450℃; Reagent/catalyst; Gas phase; |
Conditions | Yield |
---|---|
With NbP1.0Ox Reagent/catalyst; | 87.4% |
Stage #1: glycerol With sodium nitrate; diammonium hydrogenphosphate; water; boric acid at 360℃; Inert atmosphere; Stage #2: With copper(I) oxide; antimony(III) trioxide; ammonium metavanadate; ammonium molybdate; vanadia; copper(II) nitrate at 360℃; | 76% |
With water; oxygen at 284.84℃; Inert atmosphere; | 59.2% |
Conditions | Yield |
---|---|
With oxygen; catalyst based on molybdenum (Mo) and vanadium (V) at 309.4 - 321.7℃; Product distribution / selectivity; | A 1.8% B 86.2% |
With oxygen at 230℃; Product distribution / selectivity; | A 0.5% B 86.8% |
With silicon carbide; water; oxygen; Mo3VOx orthogonal modification at 189.84℃; Product distribution; Further Variations:; Catalysts; | |
With oxygen; mixed oxides of aluminum, molybdenum, silicon, vanadium and copper at 345℃; Gas phase; | |
With water; oxygen at 230℃; Reagent/catalyst; Flow reactor; Gas phase; |
Conditions | Yield |
---|---|
With oxygen; multimetal oxide catalyst at 274 - 316℃; Gas phase; | 86.1% |
Conditions | Yield |
---|---|
With oxygen; multimetal oxide catalyst at 274 - 316℃; Gas phase; | 86.1% |
B
acrylic acid
Conditions | Yield |
---|---|
In d(4)-methanol at 20 - 120℃; for 30h; Schlenk technique; | A 86% B n/a |
Conditions | Yield |
---|---|
With oxygen; multimetal oxide catalyst at 274 - 322℃; Gas phase; | 85.2% |
With oxygen at 340 - 348℃; Temperature; | 76.6% |
With oxygen; MmNnXxOo*with*A=Mo,*M=V,*N=Te,*X=Nb,*a=1,*m=0.01-1.0,*n=0.01-1.0,*n=0.01-1.0,*x=0.01-1.0,*o*is*dependent*on*the*oxidation*state*of*other*elements In water at 340 - 370℃; for 0.000833333h; | 17.7% |
With oxygen at 140 - 320℃; under 1350.14 - 1575.16 Torr; Product distribution / selectivity; |
Conditions | Yield |
---|---|
With oxygen; multimetal oxide catalyst at 274 - 316.5℃; Gas phase; | 85.2% |
Conditions | Yield |
---|---|
With oxygen; multimetal oxide catalyst at 281 - 320℃; Gas phase; | 85% |
Conditions | Yield |
---|---|
Stage #1: propene With oxygen; catalyst based on molybdenum (Mo) and bismuth (Bi) Stage #2: With oxygen; catalyst based on molybdenum (Mo) and vanadium (V) at 305.2 - 324.9℃; Product distribution / selectivity; | A 10.4% B 82.9% |
With oxygen Gas phase; | |
With oxygen Product distribution / selectivity; Gas phase; Industry scale; |
acrylic acid
propionic acid
Conditions | Yield |
---|---|
With hydrogen; palladium(II) complex of ferrocenylamine sulfide (2) In acetone under 4137.2 Torr; for 6h; or with catalyst 3, 1.25 h; | 100% |
With potassium hydroxide; hydrogen; K3HCo(CN)5; β‐cyclodextrin at 70℃; for 24h; | 81% |
With sodium amalgam |
Conditions | Yield |
---|---|
With thionyl chloride In N,N-dimethyl-formamide at 20℃; for 0.0833333h; Reagent/catalyst; Temperature; | 100% |
With thionyl chloride | 98% |
With oxalyl dichloride; N,N-dimethyl-formamide at 20 - 40℃; for 0.166667h; Product distribution / selectivity; | 96.2% |
9-Ethyl-2-phenylimidazo<1,2-a>benzimidazole
acrylic acid
3-(9-Ethyl-2-phenyl-9H-benzo[d]imidazo[1,2-a]imidazol-3-yl)-propionic acid
Conditions | Yield |
---|---|
With PPA at 70 - 90℃; | 100% |
2-(4-bromo-phenyl)-9-methyl-9H-benzo[d]imidazo[1,2-a]imidazole
acrylic acid
3-[2-(4-Bromo-phenyl)-9-methyl-9H-benzo[d]imidazo[1,2-a]imidazol-3-yl]-propionic acid
Conditions | Yield |
---|---|
With PPA | 100% |
2-isopropylimino-3-isopropyl-5-methoxy-Δ4-oxazoline
acrylic acid
1,3-diisopropyl-4-acryloxy-4-methoxy-2-oximidazoline
Conditions | Yield |
---|---|
In acetonitrile at 60℃; for 75h; | 100% |
5-bromo-2H-pyran-2-one
acrylic acid
Conditions | Yield |
---|---|
at 25℃; for 120h; Product distribution; diff. electron-rich and -poor dienophiles; | 100% |
at 25℃; for 120h; | 100% |
trisodium tris(3-sulfophenyl)phosphine
acrylic acid
C21H16O11PS3(3-)*3Na(1+)
Conditions | Yield |
---|---|
In water | 100% |
trisodium tris(3-sulfophenyl)phosphine
acrylic acid
C21H15(2)HO11PS3(3-)*3Na(1+)
Conditions | Yield |
---|---|
With water-d2 | 100% |
sodium 3-(diphenylphosphanyl)benzenesulfonate
acrylic acid
C21H18O5PS(1-)*Na(1+)
Conditions | Yield |
---|---|
In water | 100% |
sodium 3-(diphenylphosphanyl)benzenesulfonate
acrylic acid
C21H17(2)HO5PS(1-)*Na(1+)
Conditions | Yield |
---|---|
With water-d2 | 100% |
Conditions | Yield |
---|---|
With triethylamine; PdCl2(4,4'-bis(n-C10F21CH2OCH2)-2,2'-bpy) In N,N-dimethyl-formamide at 140℃; for 3h; Heck reaction; | 100% |
With potassium carbonate; palladium dichloride In water at 20 - 100℃; Heck reaction; Inert atmosphere; | 99% |
With potassium hydroxide In water at 90℃; for 5h; Mizoroki-Heck reaction; | 99% |
Conditions | Yield |
---|---|
With tributyl-amine; (silica)CH2CH2CH2CN*Pd(0) In N,N-dimethyl-formamide at 100℃; for 10.5h; Heck reaction; | 100% |
With potassium hydroxide; PS-PEG-NH-C(O)C6H4PPh2-PdCl(η3-C3H5) In toluene at 50℃; Heck reaction; | 98% |
With tri-n-propylamine; triphenylphosphine; 3-methyl-1-[2-(perfluorodecyl)ethyl]imidazolium iodide; palladium diacetate In various solvent(s) at 120℃; for 2h; Mizoroki-Heck arylation; | 98% |
acrylic acid
Conditions | Yield |
---|---|
In ethanol at 50℃; for 16.5h; Addition; Michael addition; | 100% |
6-(tetrahydropyran-2-yloxy)hex-1-ene
acrylic acid
Conditions | Yield |
---|---|
With tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride In dichloromethane at 40℃; for 15h; | 100% |
1-acryloyloxy-adamantane
acrylic acid
adamantane-modified poly(acrylic acid), degree of adamantane groups 7.17 percent, radical polymerization ; monomer(s): 1-acryloyloxyadamantane; acrylic acid
Conditions | Yield |
---|---|
With 2,2'-azobis(isobutyronitrile) In methanol at 60℃; for 24h; | 100% |
Conditions | Yield |
---|---|
Stage #1: 3-(acryloyloxy)-2-hydroxypropyl methacrylate; 3-(acryloyloxy)-2-hydroxypropyl methacrylate (cross-linked); mixture of; 2-propenamide; acrylic acid In water for 0.0333333h; pH=7.3; sodium phosphate buffer; sonication; Stage #2: With bis(2-ethylhexyl) sulfosuccinate; BRIJ 30 In hexane; water at 20℃; for 0.333333h; sonication; Stage #3: With ammonium peroxydisulfate; N,N,N,N,-tetramethylethylenediamine In hexane; water at 20℃; for 12h; | 100% |
Conditions | Yield |
---|---|
With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; triethylamine In dichloromethane at 20℃; for 24h; | 100% |
benzyl dithiobenzoate
acrylic acid
Conditions | Yield |
---|---|
With 4,4'-dicyano-4,4'-azo-di-valeric acid In ethanol at 95℃; for 1h; | 100% |
Conditions | Yield |
---|---|
In benzene | 100% |
In benzene | 100% |
92% |
acrylic acid
Conditions | Yield |
---|---|
With H(1+) In perchloric acid aq. HClO4; to the soln. of Co-compd. in aq. HClO4 was added an org. compd.; after 20 min the soln. was dild. with H2O; the react. mixt. was absorbed onto an ion-exchange column; washing with aq. HClO4, elution with NaClO4 (pH 2);; Ba(NO3)2 and K2SO4 were added; KClO4 and BaSO4 were removed by fitration; the soln. was condensed by rotoevapn. at 30°C and was filtered; addn. of HClO4, standing overnight at 8°C; recrystn. from HClO4, cooling for 4 h at the same temp.;; | 100% |
2-[2-(heptafluoropropoxy)-tetrafluoroethyl]-ethyl alcohol
acrylic acid
acrylic acid 3,3,4,4-tetrafluoro-4-heptafluoropropyloxy-butyl ester
Conditions | Yield |
---|---|
toluene-4-sulfonic acid | 100% |
2-methylbenzene-1,4-diol; toluene-4-sulfonic acid In cyclohexane at 85℃; for 24h; Dean-Stark trap; | 83% |
methyl 5-amino-3-tert-butyl-2-methoxybenzoate
acrylic acid
3-(3-tert-butyl-4-methoxy-5-(methoxycarbonyl)phenylamino)propanoic acid
Conditions | Yield |
---|---|
In toluene for 24h; Reflux; | 100% |
In toluene for 24h; Heating / reflux; | |
In toluene for 24h; Heating / reflux; | |
In toluene for 24h; Heating / reflux; |
N,N-dimethylhydroxylamine hydrochloride
acrylic acid
3-(dimethylazinoyl)propanoic acid
Conditions | Yield |
---|---|
With triethylamine In methanol at 20℃; | 100% |
acrylic acid
methyl (E)-4-(benzyloxy)-6-(2-carboxyvinyl)-1,3-benzodioxole-5-carboxylate
Conditions | Yield |
---|---|
With tributyl-amine; palladium diacetate; tetra-(n-butyl)ammonium iodide In N,N-dimethyl-formamide at 100℃; for 2.5h; Heck reaction; Inert atmosphere; | 100% |
N-(2,6-dibromo-4-heptafluoroisopropylphenyl)-3-amino-2-fluorobenzamide
acrylic acid
3-(3-(2,6-dibromo-4-(perfluoropropan-2-yl)phenylcarbamoyl)-2-fluorophenylamino)propanoic acid
Conditions | Yield |
---|---|
at 60 - 80℃; for 3h; | 100% |
4-iodobenzoic acid
acrylic acid
4-(2-carboxyvinyl)benzoic acid
Conditions | Yield |
---|---|
With D-glucose; palladium diacetate; triethylamine In water; acetonitrile at 100℃; for 16h; Sealed tube; | 100% |
With sodium carbonate In water at 100℃; for 24h; Mizoroki-Heck reaction; | 94.9% |
With tributyl-amine; potassium carbonate In N,N-dimethyl-formamide Heck Reaction; Green chemistry; | 73% |
Conditions | Yield |
---|---|
at 20 - 35℃; for 1.05h; Sealed reactor; | 100% |
With hydroquinone at 40 - 100℃; under 760.051 Torr; for 2h; Temperature; Reagent/catalyst; Autoclave; | 96% |
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