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Cas:7452-79-1
Min.Order:1 Kilogram
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inquiryThe company has a professional R & D team, mature technology, very competitive prices and stable high quality products for customers to order high quality and low price product efforts! Appearance:White or off-white Solid Storage:Sealed, dry, m
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:7452-79-1
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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:7452-79-1
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:7452-79-1
Min.Order:5 Kiloliter
FOB Price: $1.2 / 5.0
Type:Manufacturers
inquiryLIDE PHARMACEUTICALS LIMITED is a professional chemicals and APIs leading manufacturer in China. Our core business line covers APIs, Intermediates, Herb extract, etc.
Cas:7452-79-1
Min.Order:1 Kilogram
FOB Price: $0.9 / 1.0
Type:Lab/Research institutions
inquiryProduct Name: Ethyl 2-methylbutyrate Synonyms: ethyl-2-methylbutyrate(flammableliquids,n.o.s.);RARECHEM AL BI 0133;2-METHYLBUTYRIC ACID ETHYL ESTER;ETHYL 2-METHYLBUTANOATE;ETHYL 2-METHYLBUTYRATE;ETHYL DL-2-METHYLBUTYRATE;FEMA 2443;DL-2
Cas:7452-79-1
Min.Order:1 Kilogram
FOB Price: $8900.0
Type:Lab/Research institutions
inquiryProduct Description Product website: http://www.finerchem.com Product Name Ethyl 2-methylbutyrate CAS No. 7452-79-1
Cas:7452-79-1
Min.Order:1 Metric Ton
FOB Price: $12.0
Type:Lab/Research institutions
inquiryOur advantages: 1, High quality with competitive price: 1) Standard:BP/USP/EP/Enterprise standard 2) All Purity≥99% 3) We are manufacturer and can provide high quality products with factory price. 2, Fast and safe delivery 1) Parcel can be sent
Cas:7452-79-1
Min.Order:1 Kilogram
FOB Price: $9.0 / 99.0
Type:Trading Company
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:7452-79-1
Min.Order:1 Kilogram
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Type:Trading Company
inquirySynonyms: 2-Metilbutirato de etilo; Ethyl 2-methylbutanoate Molecular Formula: C7H14O2 Molecular Weight: 130.18
Cas:7452-79-1
Min.Order:5 Metric Ton
FOB Price: $1.0 / 2.0
Type:Other
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Cas:7452-79-1
Min.Order:1 Kilogram
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Type:Lab/Research institutions
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Cas:7452-79-1
Min.Order:10 Gram
FOB Price: $3.5
Type:Trading Company
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Cas:7452-79-1
Min.Order:1 Kilogram
FOB Price: $8.0 / 10.0
Type:Trading Company
inquiryEthyl 2-methylbutyrate CAS:7452-79-1 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 in
Cas:7452-79-1
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:7452-79-1
Min.Order:1 Kilogram
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Type:Lab/Research institutions
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Cas:7452-79-1
Min.Order:5 Metric Ton
Negotiable
Type:Manufacturers
inquiry1,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 highly qualifie
Cas:7452-79-1
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
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
Cas:7452-79-1
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiryminimum order qty. 10 gram
Cas:7452-79-1
Min.Order:10 Gram
Negotiable
Type:Trading Company
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
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Cas:7452-79-1
Min.Order:0 Metric Ton
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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
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Cas:7452-79-1
Min.Order:100 Gram
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Type:Other
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Cas:7452-79-1
Min.Order:100 Gram
FOB Price: $100.0 / 2000.0
Type:Lab/Research institutions
inquiryProduct name: Natural Ethyl 2-Methyl Butyratae CAS No.:7452-79-1 Molecule Formula:C7H14O2 Molecule Weight:130.18 Purity: 99.0% Package: 25kg/drum Description:Colorless transparent liquid Manufacture Standards:Enterprise Standard
Cas:7452-79-1
Min.Order:1 Kilogram
Negotiable
Type:Trading Company
inquiryProduct 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:7452-79-1
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
inquiryGMP standard, high purity, competitive price, in stock 1. Quick Response: within 6 hours after receiving your email. 2. Quality Guarantee: All products are strictly tested by our QC, confirmed by QA, and approved by a third-party lab in China, USA,
Conditions | Yield |
---|---|
With 10% Pd/C; hydrogen In methanol under 1500.15 Torr; Inert atmosphere; | 100% |
With methanol; sodium tetrahydroborate; meso-tetraphenylporphyrin iron(III) chloride In tetrahydrofuran at 30℃; for 2h; |
ethyl 2-methylbutyrate
Conditions | Yield |
---|---|
With C40H56N2RuSi4; hydrogen In toluene at 25℃; under 760.051 Torr; for 6h; Schlenk technique; | 99% |
With ethanol; (BQ‑NCOP)IrHCl; sodium t-butanolate at 60℃; for 12h; Inert atmosphere; Schlenk technique; Sealed tube; chemoselective reaction; | > 99 %Chromat. |
ethyl α-methyl-γ-(vinylsulfonyl)butyrate
ethyl 2-methylbutyrate
Conditions | Yield |
---|---|
With aluminium amalgam In tetrahydrofuran; water for 10h; Ambient temperature; | 60% |
Conditions | Yield |
---|---|
With sulfuric acid; toluene unter Entfernen des entstehenden Wassers; | |
With sulfuric acid at 80℃; for 2h; Product distribution / selectivity; |
(+/-)-ethyl ethylmethylmalonate
ethyl 2-methylbutyrate
Conditions | Yield |
---|---|
at 170℃; |
(+)-ethyl ethylmethylmalonate
ethyl 2-methylbutyrate
Conditions | Yield |
---|---|
at 170℃; |
2-Chlor-2-methyl-butin-(3)-saeure-aethylester
ethyl 2-methylbutyrate
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In ethanol |
ethyl (Z)-2-methyl-2-butenoate
ethyl 2-methylbutyrate
Conditions | Yield |
---|---|
With sodium hydrogen telluride In ethanol for 2h; Ambient temperature; | 9 % Spectr. |
With sodium hydrogen telluride In ethanol for 2h; Product distribution; Ambient temperature; other reagent; | 9 % Spectr. |
ethyl (Z)-2-methyl-2-butenoate
A
ethyl 2-methylbutyrate
B
Ethyl tiglate
C
ethyl 2-methylenebutyrate
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In ethanol at 20℃; for 0.0833333h; Product distribution; the formed intermediates are separated with gas chromatography and detected with 1H-NMR-spectroscopy after several times; | A 47.9 % Chromat. B 50.7 % Chromat. C 0.2 % Chromat. |
Ethyl tiglate
A
ethyl 2-methylbutyrate
B
ethyl (Z)-2-methyl-2-butenoate
C
ethyl 2-methylenebutyrate
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In ethanol at 20℃; for 0.0833333h; Product distribution; the formed intermediates are separated with gas chromatography and detected with 1H-NMR-spectroscopy after several times; | A 42.7 % Chromat. B 1.27 % Chromat. C 0.4 % Chromat. |
Conditions | Yield |
---|---|
With sodium tetrahydroborate; d(4)-methanol; meso-tetraphenylporphyrin iron(III) chloride In tetrahydrofuran at 30℃; for 1h; |
ethyl 2-methylenebutyrate
A
ethyl 2-methylbutyrate
B
ethyl (Z)-2-methyl-2-butenoate
C
Ethyl tiglate
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In ethanol at 20℃; for 0.0833333h; Product distribution; the formed intermediates are separated with gas chromatography and detected with 1H-NMR-spectroscopy after several times; | A 48.7 % Chromat. B 1.1 % Chromat. C 49.7 % Chromat. |
ethyl cyclobutylcarboxylate
A
ethyl 2-methylbutyrate
B
ethyl n-valerate
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal at 150℃; under 147102 Torr; Product distribution; the formed products are detected with gas chromatography; | A 0.7 % Chromat. B 0.3 % Chromat. |
1-methylcyclopropanecarboxylic acid ethyl ester
A
ethyl 2-methylbutyrate
B
2,2-dimethyl-propanoic acid ethyl ester
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In ethanol at 100℃; under 117681 Torr; for 48h; Product distribution; the formed products are detected with gas chromatography; | A 72 % Chromat. B 28 % Chromat. |
2-Methylcyclopropancarbonsaeureethylester
A
ethyl 2-methylbutyrate
B
Ethyl isovalerate
C
ethyl n-valerate
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal at 100℃; under 110326 Torr; for 1.2h; Product distribution; the formed products are detected with gas chromatography; | A 2 % Chromat. B 25 % Chromat. C 12 % Chromat. |
Bicyclo<1.1.0>butan-1-carbonsaeure-ethylester
A
ethyl 2-methylbutyrate
B
ethyl (Z)-2-methyl-2-butenoate
C
Ethyl tiglate
D
ethyl 2-methylenebutyrate
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In ethanol at 20℃; for 0.133333h; Product distribution; the formed intermediates are separated with gas chromatography and detected with 1H-NMR-spectroscopy after several times; | A 21 % Chromat. B 5 % Chromat. C 32 % Chromat. D 19 % Chromat. |
Bicyclo<1.1.0>butan-1-carbonsaeure-ethylester
A
ethyl 2-methylbutyrate
B
ethyl n-valerate
C
ethyl cyclobutylcarboxylate
D
1-methylcyclopropanecarboxylic acid ethyl ester
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In ethanol at 20℃; for 0.416667h; Product distribution; the formed products are detected with gas chromatography; | A 99.1 % Chromat. B 0.2 % Chromat. C 0.4 % Chromat. D 0.3 % Chromat. |
exo-Bicyclo<1.1.0>butan-2-carbonsaeure-ethylester
A
ethyl 2-methylbutyrate
B
ethyl n-valerate
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In ethanol at 20℃; for 0.416667h; Product distribution; the formed products are detected with gas chromatography; | A 95 % Chromat. B 5 % Chromat. |
trans-2-Methylcyclopropancarbonsaeureethylester
A
ethyl 2-methylbutyrate
B
Ethyl isovalerate
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal at 100℃; under 110326 Torr; for 72h; Product distribution; the formed products are detected with gas chromatography; | A 15 % Chromat. B 85 % Chromat. |
A
2-Methylbutanoic acid
B
(+)-S-3-sec-butylisoxazole
C
ethyl 2-methylbutyrate
Conditions | Yield |
---|---|
With hydroxylamine hydrochloride; sodium carbonate In ethanol for 15h; Product distribution; Heating; reaction at var. pH, racemization; |
Conditions | Yield |
---|---|
In diethylene glycol dimethyl ether at 170℃; Rate constant; |
Conditions | Yield |
---|---|
In diethylene glycol dimethyl ether at 170℃; Rate constant; |
ethyl diethyl malonate
A
(+/-)-2-methyl-1-butanol
B
ethyl 2-methylbutyrate
Conditions | Yield |
---|---|
at 250℃; unter Druck je nach den Bedingungen.Hydrogenation; |
ethyl diethyl malonate
A
methanol
B
(+/-)-2-methyl-1-butanol
C
ethyl 2-methylbutyrate
D
butan-1-ol
Conditions | Yield |
---|---|
at 250℃; unter Druck je nach den Bedingungen.Hydrogenation; |
1-butylene
ethanol
acetic acid
A
ethyl 2-methylbutyrate
B
ethyl n-valerate
Conditions | Yield |
---|---|
at 160 - 170℃; | |
at 160 - 170℃; |
hydrogenchloride
5-methyl-heptane-2,4-dione
A
ethyl 2-methylbutyrate
B
ethyl acetate
C
acetone
D
3-methyl-pentan-2-one
Conditions | Yield |
---|---|
at 60℃; |
2-methyl-2-ethyl-3-hydroxybutyric acid, ethyl ester
ethyl 2-methylbutyrate
Conditions | Yield |
---|---|
at 315℃; |
ethyl 2-methylbutyrate
carbon monoxide
2,6-xylyllithium
A
1-(2,6-Dimethyl-phenyl)-3-methyl-pentane-1,2-dione
B
m-xylene
Conditions | Yield |
---|---|
In tetrahydrofuran; Dimethyl ether at -135℃; | A 84% B 13% |
ethyl 2-methylbutyrate
carbon monoxide
2,6-xylyllithium
1-(2,6-Dimethyl-phenyl)-3-methyl-pentane-1,2-dione
Conditions | Yield |
---|---|
In tetrahydrofuran; diethyl ether; pentane at -135 - 25℃; | 84% |
ethyl 2-methylbutyrate
Phenylselenyl bromide
ethyl 2-methyl-2-phenylselanylbutanoate
Conditions | Yield |
---|---|
With n-butyllithium; diisopropylamine In tetrahydrofuran; hexane at -78℃; for 0.25h; selenenylation; | 72% |
ethyl 2-methylbutyrate
(S)-N-acetyl-L-aspartic anhydride
(S)-5-carboxymethyl-3-ethyl-3-methyltetramic acid
Conditions | Yield |
---|---|
Stage #1: ethyl 2-methylbutyrate With lithium diisopropyl amide In tetrahydrofuran; hexane; ethylbenzene at -78℃; for 0.75h; Inert atmosphere; Stage #2: (S)-N-acetyl-L-aspartic anhydride In tetrahydrofuran; hexane; ethylbenzene at -78 - 20℃; for 3.16667h; Inert atmosphere; optical yield given as %de; stereoselective reaction; | 70% |
ethyl 2-methylbutyrate
1-(3-bromopropyl)-2,5-dimethyl-1H-pyrrole
Conditions | Yield |
---|---|
Stage #1: ethyl 2-methylbutyrate With n-butyllithium; N-ethyl-N,N-diisopropylamine In tetrahydrofuran; hexane at -60 - -50℃; Inert atmosphere; Stage #2: 1-(3-bromopropyl)-2,5-dimethyl-1H-pyrrole In tetrahydrofuran; hexane at -50 - 20℃; for 2h; Stage #3: With hydroxylamine hydrochloride; potassium hydroxide In ethanol; water Reflux; Inert atmosphere; | 69% |
ethyl 2-methylbutyrate
formic acid ethyl ester
ethyl-2-formyl-2-methylbutanoate
Conditions | Yield |
---|---|
Stage #1: ethyl 2-methylbutyrate With lithium diisopropyl amide In tetrahydrofuran at -78℃; for 0.5h; Inert atmosphere; Stage #2: formic acid ethyl ester In tetrahydrofuran at -78 - 25℃; for 2.5h; Inert atmosphere; | 58% |
With lithium diisopropyl amide In tetrahydrofuran at -78℃; |
Conditions | Yield |
---|---|
With palladium diacetate; lithium hexamethyldisilazane; 2-N,N-(dimethylamino)-2'-di-tert-butylphosphino-1,1'-binaphthyl In toluene at 40℃; for 17h; | 54% |
Conditions | Yield |
---|---|
With n-butyllithium In tetrahydrofuran; hexane 1.) -78 deg C, 1 h, 2.) 20 deg C, overnight; | 51% |
Conditions | Yield |
---|---|
With palladium diacetate; lithium hexamethyldisilazane; 2-N,N-(dimethylamino)-2'-di-tert-butylphosphino-1,1'-binaphthyl In toluene at 80℃; for 0.5h; | 48% |
Conditions | Yield |
---|---|
Stage #1: ethyl 2-methylbutyrate With bromine; phosphorus tribromide at 75℃; Stage #2: With ethanol for 1h; Reflux; | 33% |
ethyl 2-methylbutyrate
Conditions | Yield |
---|---|
With sodium methylate at 70℃; Microwave irradiation; | 17% |
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride; diethyl ether | |
With lithium aluminium tetrahydride In tetrahydrofuran at 20℃; for 6h; |
ethyl 2-methylbutyrate
5-hydroxy-3,6-dimethyl-octan-4-one
Conditions | Yield |
---|---|
With diethyl ether; sodium |
ethyl 2-methylbutyrate
ethyl α-methyl-α-ethylvalerate
Conditions | Yield |
---|---|
With diethyl ether; triphenylmethyl sodium Einw. von Propyljodid auf das Reaktionsprodukt; |
ethyl 2-methylbutyrate
diethyl 2-ethyl-2-methyl-3-oxobutanedioate
Conditions | Yield |
---|---|
With diethyl ether; triphenylmethyl sodium Anschliessend Behandeln mit Oxalsaeure-diaethylester.; |
Conditions | Yield |
---|---|
With diethyl ether anschliessendes Behandeln mit Benzylbromid; |
ethyl 2-methylbutyrate
2-benzoyl-2-methyl-butyric acid ethyl ester
Conditions | Yield |
---|---|
With diethyl ether; triphenylmethyl sodium anschliessend Behandeln mit Benzoylchlorid; |
ethyl 2-methylbutyrate
2-methyl-2-[2]pyridyl-butyric acid ethyl ester
Conditions | Yield |
---|---|
With diethyl ether; triphenylmethyl sodium Erhitzen des Reaktionsgemisches mit 2-Brom-pyridin in Decalin auf 180grad; (+-)-2-methyl-2-<2>pyridyl-butyric acid ethyl ester; |
Conditions | Yield |
---|---|
With 1,4-dioxane; sodium hydride | |
With sodium hydride In 1,4-dioxane |
Conditions | Yield |
---|---|
With diethyl ether; triphenylmethyl sodium |
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