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Cas:88-09-5
Min.Order:1 Kilogram
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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
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Cas:88-09-5
Min.Order:5 Kiloliter
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Type:Manufacturers
inquiryProduct Name: 2-Ethylbutyric acid Synonyms: 2-Ethylbutansαure;2-Ethylbuttersαure;2-ethylbutyric;2-ethyl-butyricaci;2-Ethylbutyricaicd;3-Pentanecarboxylic acid;3-pentanecarboxylicacid;Acetic acid, diethyl- CAS: 88-09-5 MF: C6H12O2 MW
Cas:88-09-5
Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiryOur advantages: 1. All inquiries will be replied within 12 hours. 2. Dedication to quality, supply & service. 3. Strictly on selecting raw materials. 4. Reasonable & competitive price, fast lead time. 5. Sample is available for your eva
Cas:88-09-5
Min.Order:1 Kilogram
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inquiryWITH 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
Cas:88-09-5
Min.Order:1 Kilogram
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inquiry1. Product advantages High purity, all above 98.5%, no impurities after dissolution We will test each batch to ensure quality OEM and private brand services designed for free Various cap colors available We can also provide MT1 peptide powd
Cas:88-09-5
Min.Order:1 Kilogram
FOB Price: $20.0 / 25.0
Type:Trading Company
inquiryChemical Name:2-Ethylbutyric acid CAS No.:88-09-5 Molecular Formula: C6H12O2 Molecular Weight:116.16 Appearance:Colorless liquid Appearance:Colorless liquid Storage:Preserve in well-closed, light-resistant and airtight containers. Package:2
1.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
Cas:88-09-5
Min.Order:1 Gram
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Type:Lab/Research institutions
inquiry2-Ethylbutyric acid CAS:88-09-5 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 intermed
Cas:88-09-5
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
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
Cas:88-09-5
Min.Order:1 Kilogram
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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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Cas:88-09-5
Min.Order:10 Kilogram
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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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Cas:88-09-5
Min.Order:1 Gram
FOB Price: $1.0
Type:Lab/Research institutions
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
Cas:88-09-5
Min.Order:10 Gram
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Type:Lab/Research institutions
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:88-09-5
Min.Order:100 Gram
FOB Price: $100.0 / 2000.0
Type:Lab/Research institutions
inquirysuperior quality Appearance: clear colorless to light yellow liquid 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:Used as Pharmaceutical Interme
Product name: 2-Ethylbutyric Acid CAS No.:88-09-5 Molecule Formula:C6H12O2 Molecule Weight:116.15 Purity: 99% Package: 200kg/drum Description:Colorless liquid Manufacture Standards:Enterprise Standard TESTING ITEMS
Cas:88-09-5
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
inquiry2-Ethylbutyric acid Basic information Product Name: 2-Ethylbutyric acid Synonyms: (C2H5)2CHCOOH;2-ethyl-butanoicaci;2-Ethylbutansαure;2-Ethylbuttersαure;2-ethylbutyric;2-ethyl-butyricaci;2-Ethylbutyricaicd;3-Pentanecarboxylic acid
factory?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
Cas:88-09-5
Min.Order:1 Kilogram
FOB Price: $18.0 / 20.0
Type:Trading Company
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
Shandong 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
Cas:88-09-5
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
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:88-09-5
Min.Order:1 Metric Ton
FOB Price: $1.5
Type:Trading Company
inquiryAppearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
We are a Union of chemistry in China, consists of chemists,engineers, laboratories,factories in China. We organize surplus capacity of R&D and production as well as custom synthesis for chemical products and chemical business project. We are supp
Cas:88-09-5
Min.Order:1 Metric Ton
FOB Price: $1.0
Type:Trading Company
inquiryStock products, own laboratory Package:Grams, Kilograms Application:For R&D Transportation:According to customer request Port:Shanghai
Cas:88-09-5
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiryLower price, sample is available,SDS test documents are available,large stock in warehouseAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:Fine chemical intermediates, used as the main raw material for the synthe
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:88-09-5
Min.Order:100 Gram
Negotiable
Type:Lab/Research institutions
inquiryConditions | Yield |
---|---|
With poly-4-vinylpyridine In N,N-dimethyl-formamide for 0.05h; microwave irradiation; | 93% |
In water for 0.25h; Decarboxylation; microwave irradiation; | 80% |
at 170 - 180℃; |
(2-ethyl-1-butyl)boronic acid
2-Ethylbutanoic acid
Conditions | Yield |
---|---|
With chromium(VI) oxide In dichloromethane; acetic acid at 25℃; for 12h; | 92% |
Conditions | Yield |
---|---|
With N-hydroxyphthalimide; oxygen In acetonitrile at 30℃; for 3h; Schlenk technique; | 88% |
With N-hydroxyphthalimide; oxygen In acetonitrile at 30℃; under 760.051 Torr; for 3h; Catalytic behavior; Solvent; Schlenk technique; | 88% |
With calcium hypochlorite; acetic acid In water; acetonitrile Ambient temperature; | 75% |
Conditions | Yield |
---|---|
at 70℃; for 3.5h; electrolysis: nickel net anode, cylindrical stainless steel cathode; electrolyte: 1M NaOH/H2O; | 73% |
at 70℃; for 3.5h; Product distribution; electrolysis: nickel net anode, cylindrical stainless steel cathode; electrolyte: 1M NaOH/water; variation of temperature; | 73% |
Stage #1: 2-ethyl-1-butanol With [RuCl2(p-cymene)(iPr2-imy)]; tricyclohexylphosphine tetrafluoroborate; potassium hydroxide In toluene for 18h; Schlenk technique; Inert atmosphere; Reflux; Stage #2: With hydrogenchloride In water pH=1; | 60% |
With dichloro(1,5-cyclooctadiene)ruthenium(II); C30H30N3P2(1+)*Cl(1-); potassium hydroxide In toluene at 120℃; for 24h; Inert atmosphere; Schlenk technique; | 55% |
With permanganate(VII) ion |
3,3-diethyl-2-phenylsulphonyl-2-trimethylsilyloxirane
A
2-Ethylbutanoic acid
B
2-bromo-2-ethylbutanoyltrimethylsilane
C
(E)-2-ethylbut-2-enoyltrimethylsilane
D
2-ethyl-2-phenylsulphonylbutanoyltrimethylsilane
Conditions | Yield |
---|---|
With magnesium bromide ethyl etherate In diethyl ether at 0℃; for 2h; | A 19% B 57% C 9% D 0.5% |
3-Dibutoxymethyl-pentane
A
2-Ethylbutanoic acid
B
butyl 2-ethylbutyrate
C
butyric acid
D
butan-1-ol
Conditions | Yield |
---|---|
With oxygen; cobalt(II) acetate at 90℃; under 750.06 Torr; Mechanism; Rate constant; other pressure; | A 2% B 6% C 10% D 46% |
ethyl 2,2-diethyl-3-oxobutanoate
A
2-Ethylbutanoic acid
B
3-ethyl-2-pentanone
Conditions | Yield |
---|---|
With barium dihydroxide In water for 18h; Heating; | A 10% B 38% |
carbon monoxide
pentane
A
2-Ethylbutanoic acid
B
2-Methylpentanoic acid
Conditions | Yield |
---|---|
With potassium peroxodisulfate; Cu(1,10-phenanthroline)(1,2-ethanediphosphonic acid); water In acetonitrile at 60℃; under 15201 Torr; for 4h; Autoclave; High pressure; Overall yield = 35.8 %Chromat.; | A 10.6% B 24% |
With dipotassium peroxodisulfate; BF4(1-)*C24H51BCu3N3O16(1+)*2H2O; water In acetonitrile at 60℃; under 15201 Torr; for 6h; Autoclave; | A 8.6% B 17% |
With dipotassium peroxodisulfate; C26H38Cu3N4O16; water In acetonitrile at 60℃; for 6h; Reagent/catalyst; Autoclave; Green chemistry; | A 7.4% B 17.2% |
peracetic acid
hex-3-yne
A
2-Ethylbutanoic acid
B
propionic acid
diethyl ether
allyl 2-ethylbutyrate
A
allylbenzene
B
2-Ethylbutanoic acid
C
2-ethyl-1,1-diphenylbutanol
Conditions | Yield |
---|---|
With ethanol man verseift das erhaltene Nitril durch Kochen mit waessr.-alkoholischer Kalilauge; |
Conditions | Yield |
---|---|
With peracetic acid; acetic acid |
Conditions | Yield |
---|---|
With potassium hydroxide; potassium acetate at 370℃; unter Zutritt von Luft; |
2-ethyl-3-bromo-butyric acid
2-Ethylbutanoic acid
Conditions | Yield |
---|---|
With sodium amalgam; water man haelt die Loesung durch Zugabe von verduennter Schwefelsaeure bei ganz schwach alkalischer Reaktion; |
Conditions | Yield |
---|---|
Destillation; |
Conditions | Yield |
---|---|
With hydrogenchloride at 160℃; |
2,2-diethyl-acetoacetic acid methyl ester
A
2-Ethylbutanoic acid
B
3-ethyl-2-pentanone
Conditions | Yield |
---|---|
With sodium hydroxide |
diethyl malonic acid
A
2-Ethylbutanoic acid
B
methylammonium carbonate
Conditions | Yield |
---|---|
at 170 - 180℃; |
Conditions | Yield |
---|---|
at 150℃; |
Conditions | Yield |
---|---|
With sodium Man erhitzt den erhaltenen Natriumacetessigester mit Aethyljodid auf 100grad , destilliert das Reaktionsprodukt, behandelt den 151grad siedende Aethylester mit siedendem Barytwasser, diesen verseift man durch alkoh.Kalilauge; | |
With sodium Erhitzen des Reaktionsprodukts mit Aethyljodid auf 100grad, Destillieren; |
Conditions | Yield |
---|---|
With sodium amide In n-heptane at 240 - 250℃; |
Conditions | Yield |
---|---|
With phosphoric acid |
ethyl 2-ethyl-2-cyanobutyrate
A
2-Ethylbutanoic acid
B
ethyl 2-ethylbutanoate
Conditions | Yield |
---|---|
With potassium In N,N,N,N,N,N-hexamethylphosphoric triamide; diethyl ether at 0℃; |
Conditions | Yield |
---|---|
Yield given. Multistep reaction; |
hexane
carbon monoxide
A
2-Ethylbutanoic acid
B
2-Methylpentanoic acid
C
hexanoic acid
Conditions | Yield |
---|---|
With dipotassium peroxodisulfate; palladium diacetate In methanol; trifluoroacetic acid at 80℃; under 22800 Torr; for 20h; Yield given. Yields of byproduct given; |
1-penten
carbon monoxide
A
2-Ethylbutanoic acid
B
2,2-dimethylbutyric acid
C
Trimethylacetic acid
Conditions | Yield |
---|---|
With sulfuric acid; silver(l) oxide at 30℃; under 760 Torr; for 4h; Product distribution; | A 9 % Turnov. B 74 % Turnov. C 7 % Turnov. |
carbon monoxide
2-pentene
A
2-Ethylbutanoic acid
B
2-Methylpentanoic acid
C
hexanoic acid
Conditions | Yield |
---|---|
With water; bis-triphenylphosphine-palladium(II) chloride; triphenylphosphine In 1,4-dioxane at 95℃; under 15200 Torr; for 4h; Product distribution; Rate constant; other catalyst, time; |
diethylketene
2-Ethylbutanoic acid
Conditions | Yield |
---|---|
With water In acetonitrile at 20℃; Rate constant; var. H2O conc.; |
Conditions | Yield |
---|---|
Hydrogenation; |
diethylbarbituric acid
A
2-Ethylbutanoic acid
B
ammonia
C
methylammonium carbonate
Conditions | Yield |
---|---|
In toluene mixt. 2-ethylbutanoic acid (6 equiv.) and zinc oxide (4 equiv.) and toluene heated with stirring for 3 h (water removed); product filtered, solvent removed from filtrate; elem. anal.; | 99% |
2-Ethylbutanoic acid
2-ethylbutyric anhydride
Conditions | Yield |
---|---|
With triethylamine; chlorophosphoric acid diphenyl ester In dichloromethane at 20℃; for 0.25h; | 98.2% |
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20 - 25℃; | 78% |
With sulfuric acid; acetic anhydride |
Conditions | Yield |
---|---|
tetrachlorobis(tetrahydrofuran)hafnium(IV) In toluene for 60h; Heating; | 98% |
With molecualar sevies 4A; tetrachlorobis(tetrahydrofuran)hafnium(IV) In toluene at 120℃; for 60h; | 98% |
Conditions | Yield |
---|---|
With tetra-N-butylammonium tribromide for 3h; Inert atmosphere; Reflux; | 98% |
With dimesitylammonium pentafluorobenzenesulfonate In n-heptane at 80℃; for 24h; | 94% |
With N-butyl-2,4-dinitroanilinium p-toluenesulfonate In 2,2,4-trimethylpentane for 22h; Reflux; | 54% |
With 2-oleamido-5-nitro-pyridinium p-toluenesulfonate In 2,2,4-trimethylpentane for 48h; Reflux; | 50% |
2-Ethylbutanoic acid
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 20h; Inert atmosphere; | 98% |
Conditions | Yield |
---|---|
Stage #1: 2-Ethylbutanoic acid With N,N'-carbonyl diimidazole In tetrahydrofuran at 20℃; for 0.5h; Stage #2: N,O-dimethylhydroxylamine*hydrochloride With triethylamine In tetrahydrofuran at 20℃; for 6h; Reflux; | 98% |
With 1,1'-carbonyldiimidazole In dichloromethane at 0 - 20℃; |
Conditions | Yield |
---|---|
With sulfuric acid | 95% |
With sulfuric acid for 10h; | 10% |
With sulfuric acid | |
With thionyl chloride at 80℃; | |
With thionyl chloride at 80℃; |
Conditions | Yield |
---|---|
With 4,5,6,7-tetrachlorobenzo[d][1,3,2]dioxaborole In toluene for 24h; Heating; | 93% |
With ammonium chloride |
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 19h; Inert atmosphere; | 93% |
2-Ethylbutanoic acid
2',3',5'-tri-O-acetylnebularine
(2R,3R,4R,5R)-2-(acetoxymethyl)-5-(6-(pentan-3-yl)-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate
Conditions | Yield |
---|---|
With ammonium peroxydisulfate; silver nitrate In dichloromethane; water at 20℃; for 6h; Minisci Aromatic Substitution; regioselective reaction; | 92% |
2-Ethylbutanoic acid
Conditions | Yield |
---|---|
With 4-methyl-morpholine; HATU for 1h; | 92% |
2-Ethylbutanoic acid
1,3-dihydro-1-(1-methylethenyl)-2H-benzimidazol-2-one
1-(2-ethylbutanoyl)-3-(prop-1-en-2-yl)-1H-benzo[d]imidazol-2(3H)-one
Conditions | Yield |
---|---|
Stage #1: 2-Ethylbutanoic acid; 1,3-dihydro-1-(1-methylethenyl)-2H-benzimidazol-2-one With triethylamine In dichloromethane for 0.0833333h; Inert atmosphere; Cooling with ice; Stage #2: With bis(trichloromethyl) carbonate In dichloromethane at 20℃; Inert atmosphere; | 91% |
2-Ethylbutanoic acid
benzo[e][1,2,3]oxathiazine 2,2-dioxide
Conditions | Yield |
---|---|
With dipotassium peroxodisulfate; silver nitrate In water; acetonitrile at 60℃; for 48h; | 91% |
2-Ethylbutanoic acid
Conditions | Yield |
---|---|
With 2,3-dicyano-5,6-dichloro-p-benzoquinone In ethanol at 20 - 25℃; for 24h; Irradiation; | 90% |
Conditions | Yield |
---|---|
With dipotassium peroxodisulfate; copper; silver nitrate In water; acetonitrile at 90℃; for 12h; | 89% |
Conditions | Yield |
---|---|
With diethylamino-sulfur trifluoride In dichloromethane at 0℃; for 0.25h; Fluorination; | 88% |
Conditions | Yield |
---|---|
With bis-[(trifluoroacetoxy)iodo]benzene In acetonitrile at 20℃; for 12h; Inert atmosphere; Irradiation; Schlenk technique; | 88% |
2-Ethylbutanoic acid
5-chloro-2-isocyano-1,1’-biphenyl
Conditions | Yield |
---|---|
With potassium phosphate; dipotassium peroxodisulfate; silver carbonate In water; acetonitrile at 70℃; for 3h; Inert atmosphere; | 87% |
2-Ethylbutanoic acid
dodecacarbonyl-triangulo-triruthenium
{Ru2(O2CCH(C2H5)CH2CH3)2(CO)4(P(C6H5)3)2}
Conditions | Yield |
---|---|
With triphenylphosphine In tetrahydrofuran under N2; Ru-compd. and excess of acid heated at reflux for 4h, addn. of PPh3, mixt. heated for a further 20 min; recrystd. (CH2Cl2/EtOH, open conditions); elem. anal.; | 86% |
2-Ethylbutanoic acid
1-(3,4-diamino-5-(3-fluorophenyl)pyridin-2-yl)piperidine-3-carboxamide
Conditions | Yield |
---|---|
With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; 1,8-diazabicyclo[5.4.0]undec-7-ene In N,N-dimethyl-formamide at 180℃; for 0.2h; Inert atmosphere; Sealed tube; Microwave irradiation; | 86% |
Conditions | Yield |
---|---|
With thionyl chloride | 85% |
With phosphorus trichloride | |
With thionyl chloride |
Conditions | Yield |
---|---|
With benzenesulfonyl chloride | 85% |
With pyridine; benzenesulfonyl chloride Ambient temperature; | 72% |
Conditions | Yield |
---|---|
With dipotassium peroxodisulfate; silver nitrate In dichloromethane; water at 20℃; for 8h; | 85% |
With ammonium peroxydisulfate; anthocyanin In dichloromethane; water at 20℃; Minisci Aromatic Substitution; Irradiation; Green chemistry; | 59% |
2-Ethylbutanoic acid
A
2-ethyl-N-butylamine
B
bis(2-ethylbutyl)amine
C
2-ethylbutanamide
Conditions | Yield |
---|---|
Stage #1: 2-Ethylbutanoic acid With cyclopentyl methyl ether; ammonia at 200℃; under 4500.45 Torr; Sealed tube; Green chemistry; Stage #2: With cyclopentyl methyl ether; ammonia; hydrogen at 200℃; under 42004.2 Torr; for 48h; Cooling with ice; Green chemistry; | A 85% B 3% C 9% |
2-Ethylbutanoic acid
methyl 2-isocyano-3,3-diphenyl acrylate
Conditions | Yield |
---|---|
With potassium phosphate; dipotassium peroxodisulfate; silver carbonate In water; acetonitrile at 70℃; for 4h; Inert atmosphere; | 84% |
2-Ethylbutanoic acid
(E)-3-phenylacrylic acid
3-Aethyl-1-phenyl-penten-(1)
Conditions | Yield |
---|---|
With dipotassium peroxodisulfate; copper; silver nitrate In water; acetonitrile at 90℃; for 12h; | 82% |
2-Ethylbutanoic acid
2-phenyl-1,2,3,4-tetrahydroisoquinoline
[(p-methylphenyl)sulfonylmethyl]isonitrile
Conditions | Yield |
---|---|
With diethylazodicarboxylate In dichloromethane at 20℃; for 4h; Ugi Condensation; | 82% |
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