Ethanehydrazonic acid, N-(1-methylethylidene)-, ethyl ester, (E)-

Base Information

Chemical Name:Ethanehydrazonic acid, N-(1-methylethylidene)-, ethyl ester, (E)-
CAS No.:87938-10-1
Molecular Formula:C7H14N2O
Molecular Weight:142.201
Hs Code.:

Synonyms:

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Ethanehydrazonic acid, N-(1-methylethylidene)-, ethyl ester, (E)-

Chemical Property:

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Technology Process of Ethanehydrazonic acid, N-(1-methylethylidene)-, ethyl ester, (E)-

There total 4 articles about Ethanehydrazonic acid, N-(1-methylethylidene)-, ethyl ester, (E)- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 87937-99-3
2-Ethoxy-2,5,5-trimethyl-2,5-dihydro-[1,3,4]oxadiazole

: 87938-04-3
C₈H₁₆N₂O₂

: 87938-10-1
C₇H₁₄N₂O

: 627-70-3
propan-2-one azine

Guidance literature:: In benzene; at 80 ℃; reaction time at least six half-lives;
DOI:10.1021/jo00193a006

Reference yield:

: 87937-99-3
2-Ethoxy-2,5,5-trimethyl-2,5-dihydro-[1,3,4]oxadiazole

: 187737-37-7,13987-01-4,15220-87-8,9003-07-0,676-63-1,25085-53-4
propene

: 87938-10-1
C₇H₁₄N₂O

: 627-70-3
propan-2-one azine

Guidance literature:: In benzene-d6; Yield given. Further byproducts given. Yields of byproduct given; Heating;
DOI:10.1021/jo00176a024

Reference yield:

: 87937-99-3
2-Ethoxy-2,5,5-trimethyl-2,5-dihydro-[1,3,4]oxadiazole

: 187737-37-7,13987-01-4,15220-87-8,9003-07-0,676-63-1,25085-53-4
propene

: 87938-17-8
2-(1-Ethoxy-ethoxy)-propene

: 87938-10-1
C₇H₁₄N₂O

: 141-78-6
ethyl acetate

: 627-70-3
propan-2-one azine

Guidance literature:: In benzene-d6; at 80 ℃; Product distribution; Mechanism; partial thermolysis, sealed tube, effect of oxadiazoline concentration; other oxadiazine;
DOI:10.1021/jo00176a024