DayangChem 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:629-31-2
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Lab/Research institutions
inquiry1.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
heptanal oxime CAS:629-31-2 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 intermediat
Cas:629-31-2
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
Henan 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
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:629-31-2
Min.Order:10 Gram
FOB Price: $100.0
Type:Lab/Research institutions
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
Heptanal, oxime Application:Organic Chemicals
Heptanal, oxime cas 629-31-2Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
Good Quality Package:1kg/bag Application:Medical or chemical Transportation:Air/Train/Sea Port:Shenzhen
Known for its best quality and competitve price, this chemicals we offered is widely appreciated by our customers.Appearance:White powder Storage:keep sealed and keep from direct light Package:According client's requirements Application:pharmaceutica
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
1.Professional synthesis laboratory and production base. 2.Strong synthesis team and service team. 3.Professional data management system. 4.We provide the professional test date and product information ,ex. HNMR ,CNMR,FNMR, HPLC/G
Cas:629-31-2
Min.Order:10 Milligram
Negotiable
Type:Lab/Research institutions
inquiryWatson International Ltd' has a very strong R&D and technical capacity supported by FCAD's platform. The subsidiaries under FCAD Group have accumulated much know-how of different fine chemical branches. For example, Apnoke Scientific L
Heptanal oxime Storage:keep in dry and cool condition Package:25kg or according to cutomer's demand Application:Chemical research/pharma intermediate Transportation:By Sea,by Air,By courier like DHL or Fedx. Port:Shanghai/Shenzhen
FINETECH INDUSTRY LIMITED is a LONDON based CRO company providing drug discovery & development services to worldwide clients. FINETECH INDUSTRY LIMITED supplies the heptanal oxime, CAS:629-31-2 with the most competitive price and the best quality. We
Good Price, high main content Application:Medical intermediate; Used in organic synthesis
Supply top quality products with a reasonable price Application:api
Heptanal, oximeAppearance:Off white to slight yellow solid Storage:Stored in shaded, cool and dry places Package:1L 5L 10L 25L bottle Application:pharma intermediate Transportation:Handle with cares to avoid damaging the packages. Protect them from s
Conditions | Yield |
---|---|
With acetic acid; acetone oxime at 110℃; for 1.5h; | 100% |
With acetylhydroxamic acid; boron trifluoride diethyl etherate In methanol for 0.1h; Microwave irradiation; Sealed tube; | 82% |
With hydroxylamine hydrochloride; sodium acetate In ethanol; water at 0 - 20℃; | 76% |
1-nitro-1-heptene
1-heptanal oxime
Conditions | Yield |
---|---|
With tetrabutylammonium tetrafluoroborate In acetic acid; acetonitrile Reduction; Electrolysis; | 94% |
Conditions | Yield |
---|---|
With carbon monoxide; water; copper (I) acetate; Trimethylenediamine |
(E)-1-nitro-1-heptene
1-heptanal oxime
Conditions | Yield |
---|---|
With sodium dithionite; 1,1’-di-n-octyl-4,4’-bipyridinium dibromide In water; ethyl acetate | 78.7 % Chromat. |
With sodium dithionite; 1,1’-di-n-octyl-4,4’-bipyridinium dibromide In water; ethyl acetate Product distribution; Mechanism; chemical and photochemical reduction of other nitroalkenes; var. cond.; | 78.7 % Chromat. |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 75 percent / trifluoroacetic acid anhydride; Et3N / CH2Cl2 / 0.83 h 2: 94 percent / n-Bu4NBF4 / acetonitrile; acetic acid / Electrolysis View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 99 percent / KOBu-t / tetrahydrofuran; 2-methyl-propan-2-ol 2: 75 percent / trifluoroacetic acid anhydride; Et3N / CH2Cl2 / 0.83 h 3: 94 percent / n-Bu4NBF4 / acetonitrile; acetic acid / Electrolysis View Scheme |
Conditions | Yield |
---|---|
With chlorosulfonic acid In toluene at 90℃; for 0.5h; | 99% |
With N-trifluoroacetylimidazole In tetrahydrofuran for 2h; Heating; | 96% |
With cerium(IV) oxide In o-xylene at 160℃; for 2h; Dean-Stark; Inert atmosphere; | 95% |
Conditions | Yield |
---|---|
With sodium hypochlorite In dichloromethane for 240h; Ambient temperature; | 95% |
Conditions | Yield |
---|---|
With poly[4-vinyl-N,N-dichlorobenzenesulfonamide] In tetrachloromethane at 40℃; for 5h; | 90% |
With CuCl*Kieselghur; oxygen In dichloromethane at 20℃; for 0.416667h; | 89% |
With iron(III) chloride In N,N-dimethyl-formamide at 25℃; for 0.2h; sonication; | 86% |
Conditions | Yield |
---|---|
With butyl triphenylphosphonium tetraborate at 20℃; for 0.2h; | 89% |
With 1-benzyl-1-azonia-4-azabicyclo[2.2.2]octane tetrahydroborate In tert-butyl alcohol at 20℃; for 0.6h; Reduction; | 83% |
With hydrogenchloride; sodium cyanoborohydride In methanol | |
With sodium tetrahydroborate; acetic acid In tetrahydrofuran at 20℃; for 4h; Reduction; | |
With triethylsilane In chloroform Reduction; |
Conditions | Yield |
---|---|
With nickel(II) chloride hexahydrate In para-xylene at 155℃; for 18h; Inert atmosphere; | 89% |
Conditions | Yield |
---|---|
With acetic acid; acetone oxime at 110℃; for 1.5h; | 100% |
With acetylhydroxamic acid; boron trifluoride diethyl etherate In methanol for 0.1h; Microwave irradiation; Sealed tube; | 82% |
With hydroxylamine hydrochloride; sodium acetate In ethanol; water at 0 - 20℃; | 76% |
1-nitro-1-heptene
1-heptanal oxime
Conditions | Yield |
---|---|
With tetrabutylammonium tetrafluoroborate In acetic acid; acetonitrile Reduction; Electrolysis; | 94% |
Conditions | Yield |
---|---|
With carbon monoxide; water; copper (I) acetate; Trimethylenediamine |
(E)-1-nitro-1-heptene
1-heptanal oxime
Conditions | Yield |
---|---|
With sodium dithionite; 1,1’-di-n-octyl-4,4’-bipyridinium dibromide In water; ethyl acetate | 78.7 % Chromat. |
With sodium dithionite; 1,1’-di-n-octyl-4,4’-bipyridinium dibromide In water; ethyl acetate Product distribution; Mechanism; chemical and photochemical reduction of other nitroalkenes; var. cond.; | 78.7 % Chromat. |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 75 percent / trifluoroacetic acid anhydride; Et3N / CH2Cl2 / 0.83 h 2: 94 percent / n-Bu4NBF4 / acetonitrile; acetic acid / Electrolysis View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 99 percent / KOBu-t / tetrahydrofuran; 2-methyl-propan-2-ol 2: 75 percent / trifluoroacetic acid anhydride; Et3N / CH2Cl2 / 0.83 h 3: 94 percent / n-Bu4NBF4 / acetonitrile; acetic acid / Electrolysis View Scheme |
Conditions | Yield |
---|---|
With chlorosulfonic acid In toluene at 90℃; for 0.5h; | 99% |
With N-trifluoroacetylimidazole In tetrahydrofuran for 2h; Heating; | 96% |
With cerium(IV) oxide In o-xylene at 160℃; for 2h; Dean-Stark; Inert atmosphere; | 95% |
Conditions | Yield |
---|---|
With sodium hypochlorite In dichloromethane for 240h; Ambient temperature; | 95% |
Conditions | Yield |
---|---|
With poly[4-vinyl-N,N-dichlorobenzenesulfonamide] In tetrachloromethane at 40℃; for 5h; | 90% |
With CuCl*Kieselghur; oxygen In dichloromethane at 20℃; for 0.416667h; | 89% |
With iron(III) chloride In N,N-dimethyl-formamide at 25℃; for 0.2h; sonication; | 86% |
Conditions | Yield |
---|---|
With butyl triphenylphosphonium tetraborate at 20℃; for 0.2h; | 89% |
With 1-benzyl-1-azonia-4-azabicyclo[2.2.2]octane tetrahydroborate In tert-butyl alcohol at 20℃; for 0.6h; Reduction; | 83% |
With hydrogenchloride; sodium cyanoborohydride In methanol | |
With sodium tetrahydroborate; acetic acid In tetrahydrofuran at 20℃; for 4h; Reduction; | |
With triethylsilane In chloroform Reduction; |
Conditions | Yield |
---|---|
With nickel(II) chloride hexahydrate In para-xylene at 155℃; for 18h; Inert atmosphere; | 89% |
1-heptanal oxime
5-n-hexyl-1H-tetrazole
Conditions | Yield |
---|---|
With diphenyl phosphoryl azide; 1,8-diazabicyclo[5.4.0]undec-7-ene In 5,5-dimethyl-1,3-cyclohexadiene for 16h; Solvent; Reflux; Green chemistry; | 89% |
With diphenyl phosphoryl azide; 1,8-diazabicyclo[5.4.0]undec-7-ene In toluene for 48h; Reflux; | 40% |
Conditions | Yield |
---|---|
With [RuCl2(η2-C6H6){P(NMe2)3}]; water at 100℃; for 3h; Inert atmosphere; Sealed tube; | 88% |
With [PdCl2{κ2-(P,N)-2-Ph2PC6H4CH=NOH}] In water at 100℃; for 24h; Reagent/catalyst; Inert atmosphere; Sealed tube; | 84% |
With cis,cis,trans-[RuCl2{κ2-(P,N)-2-Ph2PC6H4CH=NOH}2] In water at 100℃; for 5h; Sealed tube; Inert atmosphere; | 84% |
1-heptanal oxime
(1-methyl-2-propenyl)diphenylphosphine oxide
(1'R*,5R*)-5-(1'-diphenylphosphinoylethyl)-3-hexyl-4,5-dihydroisoxazole
(1'R*,5S*)-5-(1'-diphenylphosphinoylethyl)-3-hexyl-4,5-dihydroisoxazole
Conditions | Yield |
---|---|
With sodium hypochlorite In dichloromethane for 168h; Ambient temperature; | A 77% B 30% |
Conditions | Yield |
---|---|
With C54H43ClN3P2Ru(1+)*F6P(1-); caesium carbonate In toluene at 140℃; for 48h; Inert atmosphere; Schlenk technique; Green chemistry; | 74% |
1-heptanal oxime
heptanohydroxamic acid
Conditions | Yield |
---|---|
With [hydroxy(tosyloxy)iodo]benzene In chloroform at 20 - 60℃; for 0.666667h; | 68% |
Conditions | Yield |
---|---|
With potassium chloride In neat (no solvent) for 4h; Milling; Green chemistry; | 68% |
1-heptanal oxime
[bis(acetoxy)iodo]benzene
heptanoic acid acetoxy-amide
Conditions | Yield |
---|---|
In acetonitrile at 20 - 60℃; for 0.666667h; | 66% |
1-heptanal oxime
Conditions | Yield |
---|---|
Stage #1: 1-heptanal oxime With pyridine; N-chloro-succinimide In dichloromethane at 40℃; for 0.333333h; Inert atmosphere; Stage #2: 2-(acetoxymethyl)-5-(2-amino-6-ethynyl-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate With triethylamine In dichloromethane at 20℃; for 16h; Inert atmosphere; | 64% |
1-heptanal oxime
Methyl 10-undecenoate
5-(9-methyl nonanoate)-3-hexyl-Δ2-isoxazoline
Conditions | Yield |
---|---|
With sodium hypochlorite; triethylamine In dichloromethane at 10 - 20℃; for 4h; | 63% |
Conditions | Yield |
---|---|
With sodium iodide In methanol Ambient temperature; platinum electrodes, electrolysis at constant current; | 56% |
Conditions | Yield |
---|---|
With propylamine; lithium; tert-butyl alcohol In ethylenediamine at 20 - 53℃; for 1.75h; Reduction; | 55% |
With ethanol; platinum under 2206.5 Torr; Hydrogenation; | |
With ethanol; sodium |
Conditions | Yield |
---|---|
With pyridine; sodium hypochlorite In chloroform at 0℃; for 2h; Cycloaddition; | 50% |
1-heptanal oxime
methyl 2-methoxy-5-phenyl-furan-3-carboxylate
Conditions | Yield |
---|---|
With oxygen; thiamine diphosphate In dichloromethane at -20℃; for 1.5h; Irradiation; | 35% |
Conditions | Yield |
---|---|
With 1-Heptylamine; nickel kieselguhr; methyl cyclohexane at 100 - 125℃; under 73550.8 - 110326 Torr; Hydrogenation; | |
With ammonia; hydrogen; platinum at 25℃; under 2280 Torr; Hydrogenation; |
Conditions | Yield |
---|---|
With diethyl ether; nickel kieselguhr at 100 - 125℃; under 73550.8 - 110326 Torr; Hydrogenation; | |
With ethanol; nickel kieselguhr at 100 - 125℃; under 73550.8 - 110326 Torr; Hydrogenation; | |
With ethanol; nickel at 15 - 18℃; Hydrogenation; | |
With nickel kieselguhr; methyl cyclohexane at 100 - 125℃; under 73550.8 - 110326 Torr; Hydrogenation; |
Conditions | Yield |
---|---|
With trifluoroacetyl peroxide | |
(i) Cl2, (ii) O2, O3, (iii) H2, aq. NaOH, Pd-C; Multistep reaction; |
1-heptanal oxime
Conditions | Yield |
---|---|
With diethyl ether; nitrosylchloride |
Conditions | Yield |
---|---|
With sodium ethanolate |
Conditions | Yield |
---|---|
With silver(l) oxide |
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