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Cas:5281-20-9
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
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Cas:5281-20-9
Min.Order:1 Kilogram
FOB Price: $2.0
Type:Lab/Research institutions
inquiryShandong 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:5281-20-9
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
inquiryhight degree of purity Application:Fine chemical intermediates, used as the main raw material for he synthesis of various pesticides, medicines, surfactants, polymer monomers, Ond Ontifungal agents
Cas:5281-20-9
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiryCompound sourcing ServicesAgency of testing serviceFactory audit serviceFounded in Dec. 1999, Nanjing Chemlin Chemical Industrial Co.,Ltd(CHEMLIN) has been covering the business scope from trading of chemicals to custom-synthesis & Manufacturing. Co
FINETECH INDUSTRY LIMITED is a LONDON based CRO company providing drug discovery & development services to worldwide clients. FINETECH INDUSTRY LIMITED supplies the acetone hydrazone, CAS:5281-20-9 with the most competitive price and the best quality
Conditions | Yield |
---|---|
With barium(II) oxide; hydrazine In methanol at -5 - 20℃; | 89% |
With hydrazine hydrate; barium(II) oxide | |
With hydrazine |
Conditions | Yield |
---|---|
With hydrazine hydrate |
Conditions | Yield |
---|---|
With hydrazine at 100℃; | |
With hydrazine at 100℃; for 16h; Inert atmosphere; Schlenk technique; | |
With hydrazine at 100℃; for 16h; Inert atmosphere; |
Conditions | Yield |
---|---|
With potassium bromate; perchloric acid In water; acetic acid at 19.9℃; Rate constant; Kinetics; Thermodynamic data; E(a), ΔH(excit.), ΔS(excit.), ΔG(excit.); var. reagent concentrations, var. pH values; |
Conditions | Yield |
---|---|
at 100℃; |
hydrogenchloride
propan-2-one azine
A
acetone hydrazone
B
acetone
C
hydrazine
Conditions | Yield |
---|---|
at 15℃; Gleichgewicht;pH=4.60 bis 5.35; | |
at 20℃; Gleichgewicht;pH=4.60 bis 5.35; |
acetone
1-phenylbutan-1,3-dione
A
acetone hydrazone
B
2-(3'-methyl-5'-phenylpyrazol-1'-yl)-5-methyl-7-phenylpyrazolo[1,5-a]pyrimidine
C
3-methyl-5-phenylpyrazole
Conditions | Yield |
---|---|
In water for 4h; Reflux; regioselective reaction; | A 60 %Spectr. B 8 %Spectr. C 32 %Spectr. |
Conditions | Yield |
---|---|
With C24H20B(1-)*C27H39AuClN*K(1+); hydrazine at 130℃; for 14h; Inert atmosphere; |
acetone hydrazone
Dimethyl itaconate
methyl 2,2-dimethyl-1-methoxycarbonylmethylcyclopropane-1-carboxylate
Conditions | Yield |
---|---|
With iodosylbenzene In ethyl acetate at 20℃; for 1h; Green chemistry; | 100% |
Conditions | Yield |
---|---|
With iodosylbenzene In ethyl acetate at 20℃; for 1h; Green chemistry; | 100% |
acetone hydrazone
2-acetylamino-acrylic acid benzyl ester
Conditions | Yield |
---|---|
With iodosylbenzene In ethyl acetate at 20℃; for 1h; Green chemistry; | 100% |
Conditions | Yield |
---|---|
With iodosylbenzene In dichloromethane at 20℃; for 1h; Green chemistry; | 100% |
Conditions | Yield |
---|---|
With iodosylbenzene In ethyl acetate at 20℃; for 1h; Green chemistry; | 100% |
Conditions | Yield |
---|---|
With iodosylbenzene In ethyl acetate at 20℃; for 1h; Green chemistry; | 100% |
Conditions | Yield |
---|---|
With iodosylbenzene In dichloromethane at 20℃; for 1h; Green chemistry; | 100% |
Conditions | Yield |
---|---|
With iodosylbenzene In ethyl acetate at 20℃; for 1h; Solvent; Temperature; Green chemistry; | 100% |
Conditions | Yield |
---|---|
In ethanol for 2h; Heating; | 98% |
acetone hydrazone
ethyl 2-(ethoxymethylidene)-4,4,4-trifluoro-3-oxobutanoate
ethyl 3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylate
Conditions | Yield |
---|---|
In acetonitrile at 20℃; for 1.08333h; | 94% |
acetone hydrazone
benzvalene
3,3-dimethyl-cis-3,3a,4,5,6,6a-hexahydro-4,5,6-methanocyclopentapyrazole
Conditions | Yield |
---|---|
With potassium hydroxide; mercury(II) oxide In diethyl ether at 20℃; for 15h; | 93% |
acetone hydrazone
5-chloro-1,2,3-thiadiazole-4-carboxamide
Conditions | Yield |
---|---|
In ethanol for 2h; Heating; | 92% |
acetone hydrazone
Conditions | Yield |
---|---|
With MnO2 In tetrahydrofuran byproducts: N2; THF soln. of RhIr-complex was treated with an excess of Me2C=NNH2 under N2 atmosphere (Schlenk techniques), at 45°C activated MnO2 was added, mixt. was stirred for ca. 30 min; evapd., residue was taken up in hexane, filtered, filtrate concd., chromd. on a column with silylated SiO2 (N2, -20°C, eluent petroleum ether); elem. anal.; | 92% |
Conditions | Yield |
---|---|
In methanol Ambient temperature; 1.) 0 deg C, 2 h; 2.) room temperature, 24 h; | 87% |
acetone hydrazone
3-Chloro-4-(3,3,6,6-tetramethyl-1,8-dioxo-2,3,4,5,6,7,8,9-octahydro-1H-xanthen-9-yl)-benzenesulfonyl chloride
Conditions | Yield |
---|---|
In methanol Ambient temperature; | 86% |
Conditions | Yield |
---|---|
With iodosylbenzene In dichloromethane at 20℃; for 1h; Green chemistry; | 86% |
acetone hydrazone
methacrylonitrile
1,1,2-trimethyl-cyclopropanecarbonitrile
Conditions | Yield |
---|---|
With iodosylbenzene In dichloromethane at 20℃; for 1h; Green chemistry; | 84% |
acetone hydrazone
ethyl ester of 2-(5-nitro-2,4-dichlorobenzoyl)-3-ethoxyacrylic acid
2-(2,4-Dichlor-5-nitrobenzoyl)-3-(isopropylidenhydrazino)acrylsaeure-ethylester
Conditions | Yield |
---|---|
In ethanol for 0.5h; Ambient temperature; | 80% |
acetone hydrazone
norbornene
(3aR,4S,7R,7aS)-3,3-Dimethyl-3a,4,5,6,7,7a-hexahydro-3H-4,7-methano-indazole
Conditions | Yield |
---|---|
With potassium hydroxide; mercury(II) oxide In diethyl ether at 20℃; for 15h; | 79% |
acetone hydrazone
1,4-diphenyl-1,3-butadiyne
A
3,3-dimethyl-4-phenyl-5-phenylethynyl-3H-pyrazole
B
3,3-dimethyl-5-phenyl-4-(phenylethynyl)-3H-pyrazole
C
3,3,3',3'-tetramethyl-4',5'-diphenyl-4,5'-bi-3H-pyrazolyl
Conditions | Yield |
---|---|
With potassium hydroxide; mercury(II) oxide In diethyl ether 1.) reflux, 2 h, 2.) 0 deg C, 2 d; | A 2% B 76% C 8% |
With potassium hydroxide; mercury(II) oxide In diethyl ether 1.) 2h, 2.) 0 deg C, 2d; | A 2% B 76% C 8% |
With potassium hydroxide; mercury(II) oxide In diethyl ether 1.) reflux, 2 h, 2.) 0 deg C, 2 d; | A 11% B 25% C 58% |
With potassium hydroxide; mercury(II) oxide In diethyl ether 1.) 2h, 2.) 0 deg C, 2d; | A 11% B 25% C 58% |
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran Ambient temperature; | 74% |
Conditions | Yield |
---|---|
Stage #1: acetone With magnesium sulfate; hydrazine hydrate In methanol at 20℃; Stage #2: acetone hydrazone With pyridine; N-Bromosuccinimide In dichloromethane at -10 - 0℃; | 74% |
acetone hydrazone
C14H11Cl2N3O
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran at -5 - 20℃; | 71% |
Conditions | Yield |
---|---|
With potassium chloride; mercury(II) oxide In 1,4-dioxane the hydrazone was dissolved in the suspension of Hg(OAc)2 and HgO in dioxane, after cooling to room temp. the solvent was distd. in vac., and the residue was dissolved in CH2Cl2 and was added to 10 % KCl soln.; aq. phase was extd. with CH2Cl2, combined organic phases washed with water, dried over MgSO4, CH2Cl2 was distd., crystn., elem. anal.; | 71% |
Conditions | Yield |
---|---|
Stage #1: acetone With magnesium sulfate; hydrazine hydrate at 20℃; Stage #2: acetone hydrazone With N-chloro-succinimide In dichloromethane at -10 - 0℃; | 71% |
acetone hydrazone
2-oxo-N-(4-chlorophenyl)propanehydrazonoyl chloride
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran Ambient temperature; | 70% |
acetone hydrazone
dimethyl acetylenedicarboxylate
dimethyl 3,3-dimethyl-3H-pyrazole-4,5-dicarboxylate
Conditions | Yield |
---|---|
Stage #1: acetone hydrazone With iodosylbenzene In dichloromethane at -20℃; for 0.0833333h; Stage #2: dimethyl acetylenedicarboxylate In dichloromethane | 69% |
acetone hydrazone
3,3-dimethyl-5-phenyl-4-(phenylethynyl)-3H-pyrazole
3,3,3',3'-tetramethyl-4',5'-diphenyl-4,5'-bi-3H-pyrazolyl
Conditions | Yield |
---|---|
With potassium hydroxide; mercury(II) oxide In diethyl ether | 67% |
With potassium hydroxide; mercury(II) oxide In diethyl ether at 0℃; | 67% |
acetone hydrazone
N-(3-(5-mercapto-1,3,4-oxadiazol-2-yl)phenyl)-2-(propan-2-ylidene)hydrazinocarbothioamide
Conditions | Yield |
---|---|
In benzene for 3h; Reflux; | 67% |
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