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Cas:2446-84-6
Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiryWith our good experience, we offer detailed technical support and advice to assist customers. We communicate closely with customers to establish their quality requirements. Consistent Quality Our plant has strict quality control in each manufacturin
Cas:2446-84-6
Min.Order:1 Kilogram
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Type:Trading Company
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Cas:2446-84-6
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
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Cas:2446-84-6
Min.Order:10 Gram
FOB Price: $100.0
Type:Lab/Research institutions
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Cas:2446-84-6
Min.Order:1 Kilogram
FOB Price: $2.0
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
1,2-Diazenedicarboxylicacid, 1,2-dimethyl ester cas 2446-84-6Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express
Cas:2446-84-6
Min.Order:0
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inquiryfactory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
Cas:2446-84-6
Min.Order:0
Negotiable
Type:Trading Company
inquiryBest Seller, High Quality, Competitive Price, Fast Delivery, Quick ResponseAppearance:powder, or liquid Storage:Stored in room temperature, ventilated place Package:Bottle, barrel, cargo, container, etc. Application:Pharmaceuticals, intermediates, AP
Cas:2446-84-6
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inquiryFINETECH INDUSTRY LIMITED is a LONDON based CRO company providing drug discovery & development services to worldwide clients. FINETECH INDUSTRY LIMITED supplies the AZODICARBOXYLIC ACID DIMETHYL ESTER, CAS:2446-84-6 with the most competitive price an
Cas:2446-84-6
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Type:Trading Company
inquiryConditions | Yield |
---|---|
With dipotassium hydrogenphosphate for 1h; Reflux; | 98% |
C7H15N3O6Si
dimethyl azodicarboxylate
Conditions | Yield |
---|---|
In dichloromethane at 25℃; for 72h; | 75% |
N,N'-Bis-(methoxycarbonyl)-hydrazin
dimethyl azodicarboxylate
Conditions | Yield |
---|---|
With nitric acid |
azidoformiate de methyle
A
formaldehyd
B
isocyanic acid
C
dimethyl azodicarboxylate
D
methoxy isocyanate
Conditions | Yield |
---|---|
Irradiation; |
azidoformiate de methyle
A
formaldehyd
B
isocyanic acid
C
methyleneamine
D
dimethyl azodicarboxylate
E
methoxy isocyanate
Conditions | Yield |
---|---|
Product distribution; Heating; further temp., pressure, residence time; |
N,N'-Bis-(methoxycarbonyl)-hydrazin
nitric acid
dimethyl azodicarboxylate
4,2',3'-trimethyl-4'-(p-fluorobenzyl)purpurogallin
dimethyl azodicarboxylate
Conditions | Yield |
---|---|
In toluene Heating; | 100% |
2-(p-fluorobenzyloxy)tropone
dimethyl azodicarboxylate
Conditions | Yield |
---|---|
In toluene hetero-Diels Alder reaction; Heating; | 100% |
2-(o-fluorobenzyloxy)tropone
dimethyl azodicarboxylate
Conditions | Yield |
---|---|
In toluene hetero-Diels Alder reaction; Heating; | 100% |
dimethyl azodicarboxylate
1,3-Bis-(1-cyclopenta-2,4-dienylidene-2,2-dimethyl-propyl)-benzene
C34H42N4O8
Conditions | Yield |
---|---|
In dichloromethane for 1h; | 99% |
Conditions | Yield |
---|---|
With (η5-1,2,3,4,5-pentamethylcyclopentadienyl)Ir[(S,S)-N-(Ms)-1,2-diphenylethylenediamine] In toluene at 0℃; for 2.33333h; Inert atmosphere; optical yield given as %ee; enantioselective reaction; | 99% |
ethyl 2-(4-chlorophenyl)-2-cyanoacetate
dimethyl azodicarboxylate
Conditions | Yield |
---|---|
With C35H45IrN2O3S In toluene at -20℃; for 2h; Inert atmosphere; optical yield given as %ee; enantioselective reaction; | 99% |
Cyan-phenyl-essigsaeure-dimethylamid
dimethyl azodicarboxylate
C15H18N4O5
Conditions | Yield |
---|---|
With (η5-1,2,3,4,5-pentamethylcyclopentadienyl)Ir[(S,S)-N-(Ms)-1,2-diphenylethylenediamine] In toluene at 0℃; for 2.33333h; Inert atmosphere; optical yield given as %ee; enantioselective reaction; | 99% |
Conditions | Yield |
---|---|
With (η5-1,2,3,4,5-pentamethylcyclopentadienyl)Ir[(S,S)-N-(Ms)-1,2-diphenylethylenediamine] In toluene at 0℃; for 2.33333h; Inert atmosphere; optical yield given as %ee; enantioselective reaction; | 99% |
dimethyl azodicarboxylate
Conditions | Yield |
---|---|
With (R)-((4,4’-bi-1,3-benzodioxole)-5,5’-diyl)bis(bis(3,5-di-t-butyl-4-methoxyphenyl))phosphine; 2,2,2-trifluoroethanol; silver trifluoromethanesulfonate In tetrahydrofuran; N,N-dimethyl-formamide at -78 - 20℃; for 15h; Reagent/catalyst; Solvent; Temperature; Inert atmosphere; Darkness; enantioselective reaction; | 99% |
C13H11F3O2
dimethyl azodicarboxylate
Conditions | Yield |
---|---|
With (R)-((4,4’-bi-1,3-benzodioxole)-5,5’-diyl)bis(bis(3,5-di-t-butyl-4-methoxyphenyl))phosphine; 2,2,2-trifluoroethanol; silver trifluoromethanesulfonate In tetrahydrofuran; N,N-dimethyl-formamide at -78 - 20℃; for 16h; Inert atmosphere; Darkness; enantioselective reaction; | 99% |
C13H11F3O3
dimethyl azodicarboxylate
Conditions | Yield |
---|---|
With (R)-((4,4’-bi-1,3-benzodioxole)-5,5’-diyl)bis(bis(3,5-di-t-butyl-4-methoxyphenyl))phosphine; 2,2,2-trifluoroethanol; silver trifluoromethanesulfonate In tetrahydrofuran; N,N-dimethyl-formamide at -78 - 20℃; for 11h; Inert atmosphere; Darkness; enantioselective reaction; | 99% |
Conditions | Yield |
---|---|
In toluene Heating; | 98% |
Conditions | Yield |
---|---|
In toluene hetero-Diels Alder reaction; Heating; | 98% |
dimethyl azodicarboxylate
1-phenyl-propan-1-one
dimethyl 1-(1-oxo-1-phenylpropan-2-yl)hydrazine-1,2-dicarboxylate
Conditions | Yield |
---|---|
With 1,2,2,6,6-pentamethylpiperidine; tris(pentafluorophenyl)borate In toluene at 22℃; for 12h; Inert atmosphere; | 98% |
dimethyl azodicarboxylate
1-methyl-pyrrolidine-2-thione
Conditions | Yield |
---|---|
With 1,2,2,6,6-pentamethylpiperidine; tris(pentafluorophenyl)borate In toluene at 22℃; for 12h; Inert atmosphere; | 98% |
N1-<(2,5,5-Trimethyl-1,3,6-heptatrienyl)methyl>-N1,N2-hydrazindicarbonsaeure-dimethylester
dimethyl azodicarboxylate
9-<1,2-Bis(methoxycarbonyl)hydrazinomethyl>-3,3,8-trimethyl-6,7-diazatricyclo<3.2.2.02,4>non-8-en-6,7-dicarbonsaeure-dimethylester
Conditions | Yield |
---|---|
In benzene at 50℃; for 5h; | 97% |
4-hydroxy-2,3,6-trimethoxy-5H-benzo[7]annulen-5-one
dimethyl azodicarboxylate
Conditions | Yield |
---|---|
In toluene Heating; | 97% |
Conditions | Yield |
---|---|
With 1,2,2,6,6-pentamethylpiperidine; tris(pentafluorophenyl)borate In toluene at 22℃; for 12h; Inert atmosphere; | 97% |
Conditions | Yield |
---|---|
With 1,2,2,6,6-pentamethylpiperidine; tris(pentafluorophenyl)borate In toluene at 22℃; for 12h; Inert atmosphere; | 97% |
α-(1-dimethylaminovinyl)pyridine
dimethyl azodicarboxylate
C17H24N6O8
Conditions | Yield |
---|---|
In diethyl ether overnight; | 96% |
Conditions | Yield |
---|---|
96% |
2-methyl-3-pyrrolidin-1-yl-5,6-dihydro-4H-thiopyran 1,1-dioxide
dimethyl azodicarboxylate
4-(N,N'-dimethoxycarbonylhydrazino)-2-methyl-3-pyrrolidin-1-yl-5,6-dihydro-4H-thiopyran 1,1-dioxide
Conditions | Yield |
---|---|
In benzene for 72h; Ambient temperature; | 96% |
Conditions | Yield |
---|---|
With triphenylphosphine In dichloromethane at 20℃; for 24h; Mitsunobu reaction; | 96% |
4,2',3'-trimethyl-4'-(o-fluorobenzyl)purpurogallin
dimethyl azodicarboxylate
Conditions | Yield |
---|---|
In toluene Heating; | 96% |
4,2',3'-trimethyl-4'-(p-methoxybenzyl)purpurogallin
dimethyl azodicarboxylate
Conditions | Yield |
---|---|
In toluene Heating; | 96% |
dimethyl azodicarboxylate
(+)-(1R,6R)-3,7,7-Trimethyl-4-methylenbicyclo<4.1.0>hept-2-en
9-<1,2-Bis(methoxycarbonyl)hydrazinomethyl>-3,3,8-trimethyl-6,7-diazatricyclo<3.2.2.02,4>non-8-en-6,7-dicarbonsaeure-dimethylester
Conditions | Yield |
---|---|
In benzene at 50℃; for 5h; | 95% |
dimethyl azodicarboxylate
6-<5-methoxy-3,3-dimethyl-2-tetrahydrofuranyl>fulvene
N,N'-bis(methoxycarbonyl)-2,3-diaza-7-<5-methoxy-3,3-dimethyl-2-tetrahydrofuranylidene>bicyclo<2.2.1>hept-5-ene
Conditions | Yield |
---|---|
In diethyl ether at 4℃; for 120h; | 95% |
dimethyl azodicarboxylate
acetic p-nitrophenyldiazoacetic anhydride
Conditions | Yield |
---|---|
dirhodium tetraacetate In benzene at 50℃; | 95% |
Conditions | Yield |
---|---|
In toluene Heating; | 95% |
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