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Cas:1447-26-3
Min.Order:1 Kilogram
FOB Price: $1.0 / 10.0
Type:Trading Company
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Cas:1447-26-3
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
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Cas:1447-26-3
Min.Order:10 Gram
Negotiable
Type:Lab/Research institutions
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Cas:1447-26-3
Min.Order:1 Kilogram
FOB Price: $2.0
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:Beijing or Guangzhou
factory?direct?sale Application:healing drugs
Cas:1447-26-3
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiryShanghai, Run-Biotech Co., Ltd is a leading domestic pharmaceutical, biopharmaceutical, and health care products R & D outsourcing services company. As an innovation-driven and customer-focused company, Run Biotech provides a broad and integrated por
4-ethyl-2-hexyn-4-ol
A
(E)-3-ethyl-2-hexen-4-one
B
5-methyl-4-hepten-3-one
Conditions | Yield |
---|---|
With NH4NO3-exchanged zeolite HSZ-320 In chlorobenzene at 130℃; for 4h; Yield given; | A 80% B n/a |
With NH4NO3-exchanged zeolite HSZ-320 In chlorobenzene at 130℃; for 4h; Yields of byproduct given; | A 80% B n/a |
ethylmagnesium iodide
ethyl (Z)-3-ethoxybut-2-enoate
5-methyl-4-hepten-3-one
Conditions | Yield |
---|---|
With methanol; palladium on activated charcoal Hydrogenation; |
5-hydroxy-5-methyl-heptan-3-one
5-methyl-4-hepten-3-one
Conditions | Yield |
---|---|
With oxalic acid durch Destillation; | |
With oxalic acid durch Destillation; |
Conditions | Yield |
---|---|
at 25℃; Gleichgewicht und Geschwindigkeit der Reaktion; |
Conditions | Yield |
---|---|
Gleichgewicht der Umlagerung; |
sodium ethanolate
butanone
A
5-methyl-hept-5-en-3-one
B
5-methyl-4-hepten-3-one
aluminum tri-tert-butoxide
butanone
benzene
5-methyl-4-hepten-3-one
aluminum tri-tert-butoxide
butanone
benzene
A
5-methyl-hept-5-en-3-one
B
5-methyl-4-hepten-3-one
Conditions | Yield |
---|---|
With sodium ethanolate | |
With beryllium(II) chloride; benzene at 130℃; | |
With aluminum tri-tert-butoxide; benzene |
Conditions | Yield |
---|---|
With calcium carbide | |
With sodium ethanolate | |
With (Ph3P)3CoCH3 at 23 - 25℃; for 24h; |
(E)-3-methyl-pent-3-enoyl chloride
ethylzinc iodide
5-methyl-4-hepten-3-one
Conditions | Yield |
---|---|
In diethyl ether |
Conditions | Yield |
---|---|
With (Ph3P)3CoCH3 at 20 - 25℃; for 24h; Yield given. Yields of byproduct given; |
5-methyl-4-hepten-3-one
Conditions | Yield |
---|---|
With ethyl zinc iodide |
ethylmagnesium iodide
5-methyl-4-hepten-3-one
Conditions | Yield |
---|---|
With diethyl ether |
Conditions | Yield |
---|---|
at 130℃; |
butanone
benzene
A
5-methyl-hept-5-en-3-one
B
5-methyl-4-hepten-3-one
Conditions | Yield |
---|---|
at 130℃; |
hydrogenchloride
ethanol
5-methyl-hept-5-en-3-one
5-methyl-4-hepten-3-one
Conditions | Yield |
---|---|
das Gleichgewicht liegt bei 57-58prozent 3-Methyl-hepten-(3)-on-(5); |
ethanol
5-methyl-hept-5-en-3-one
phosphoric acid
5-methyl-4-hepten-3-one
Conditions | Yield |
---|---|
das Gleichgewicht liegt bei 57-58prozent 3-Methyl-hepten-(3)-on-(5); |
ethanol
5-methyl-hept-5-en-3-one
sulfuric acid
5-methyl-4-hepten-3-one
Conditions | Yield |
---|---|
das Gleichgewicht liegt bei 57-58prozent 3-Methyl-hepten-(3)-on-(5); |
diethyl ether
3ξ-methyl-pent-3-enoic acid-chloride
A
5-methyl-hept-5-en-3-one
B
5-methyl-4-hepten-3-one
Conditions | Yield |
---|---|
und beim Kochen mit 10prozentiger alkoholischer Natronlauge; |
methanol
5-methyl-hepta-1,4-dien-3-one
A
3-oxo-5-methyl-1-heptene
B
5-methyl-3-heptanone
C
5-methyl-4-hepten-3-one
Conditions | Yield |
---|---|
Hydrogenation; |
5-Hexyn-3-ol
5-methyl-4-hepten-3-one
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: CrO3, H2SO4 / acetone 2: diethyl ether View Scheme |
chloro-trimethyl-silane
5-methyl-4-hepten-3-one
1,1,1,3,3,3-hexamethyl-disilazane
Conditions | Yield |
---|---|
With piperidine In tetrahydrofuran N2-atmosphere; addn. of ketone and piperidine to soln. of Fe-complex, filtration chromy. (silicic acid, CH2Cl2), addn. of Me3SiCl and hexamethyldisilazane, stirring (45 h); solvent removal, filtration chromy. (silicic acid, pentane), recrystn. (pentane); elem. anal., mixture of diastereomers (1:1) not sepd.; | 31% |
Conditions | Yield |
---|---|
With diethyl ether |
Conditions | Yield |
---|---|
at -15 - -12℃; und Destillieren des Reaktionsprodukts mit Phthalsaeureanhydrid; |
chloroform
5-methyl-4-hepten-3-one
A
formic acid
B
acetic acid
C
propionic acid
D
butanone
Conditions | Yield |
---|---|
Beim Ozonisieren und folgenden Zersetzen mit wss.H2O2; |
5-methyl-hept-5-en-3-one
sodium diethylmalonate
5-methyl-4-hepten-3-one
A
ethanol
Conditions | Yield |
---|---|
at -15 - -12℃; Behandeln des Reaktionsprodukts mit Phthalsaeureanhydrid; |
5-methyl-4-hepten-3-one
phosphonic acid diethyl ester
5-(diethoxyphosphinoyl)-5-methylheptan-3-one
Conditions | Yield |
---|---|
With sodium ethanolate |
Conditions | Yield |
---|---|
With platinum Hydrogenation; |
potassium thioacyanate
5-methyl-4-hepten-3-one
5-isothiocyanato-5-methyl-heptan-3-one
Conditions | Yield |
---|---|
With sulfuric acid |
tris(dimethylamino)stibine
5-methyl-4-hepten-3-one
[(E)-1-Eth-(Z)-ylidene-3-methyl-pent-2-enyl]-dimethyl-amine
5-methyl-4-hepten-3-one
4,5-epoxy-5-methyl-3-heptanone
Conditions | Yield |
---|---|
With sodium hydroxide; dihydrogen peroxide In methanol for 18h; |
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