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(Z)-But-2-enedioic acid ethyl ester 2,4,4-trimethyl-3-vinyl-cyclohex-2-enyl ester

Base Information Edit
  • Chemical Name:(Z)-But-2-enedioic acid ethyl ester 2,4,4-trimethyl-3-vinyl-cyclohex-2-enyl ester
  • CAS No.:104788-47-8
  • Molecular Formula:C17H24O4
  • Molecular Weight:292.375
  • Hs Code.:
  • Mol file:104788-47-8.mol
(Z)-But-2-enedioic acid ethyl ester 2,4,4-trimethyl-3-vinyl-cyclohex-2-enyl ester

Synonyms:(Z)-But-2-enedioic acid ethyl ester 2,4,4-trimethyl-3-vinyl-cyclohex-2-enyl ester

Suppliers and Price of (Z)-But-2-enedioic acid ethyl ester 2,4,4-trimethyl-3-vinyl-cyclohex-2-enyl ester
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of (Z)-But-2-enedioic acid ethyl ester 2,4,4-trimethyl-3-vinyl-cyclohex-2-enyl ester Edit
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Technology Process of (Z)-But-2-enedioic acid ethyl ester 2,4,4-trimethyl-3-vinyl-cyclohex-2-enyl ester

There total 6 articles about (Z)-But-2-enedioic acid ethyl ester 2,4,4-trimethyl-3-vinyl-cyclohex-2-enyl ester 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:
Guidance literature:
Multi-step reaction with 6 steps
1: 1) LDA / 1) THF, -78 degC
2: 78 percent / NaH / tetrahydrofuran / 4 h / Heating
3: 79 percent / p-TsOH / benzene / 24 h / Heating
4: 96 percent / diethyl ether / 4 h / Heating
5: 70 percent / LiAlH4 / diethyl ether / 2 h / Heating
6: 67 percent / dicyclohexylcarbodiimide, 4(N,N-dimethylamino)pyridine / CH2Cl2 / 4 h / Ambient temperature
With dmap; lithium aluminium tetrahydride; sodium hydride; toluene-4-sulfonic acid; dicyclohexyl-carbodiimide; lithium diisopropyl amide; In tetrahydrofuran; diethyl ether; dichloromethane; benzene;
DOI:10.1039/c39840001423
Guidance literature:
Multi-step reaction with 5 steps
1: 78 percent / NaH / tetrahydrofuran / 4 h / Heating
2: 79 percent / p-TsOH / benzene / 24 h / Heating
3: 96 percent / diethyl ether / 4 h / Heating
4: 70 percent / LiAlH4 / diethyl ether / 2 h / Heating
5: 67 percent / dicyclohexylcarbodiimide, 4(N,N-dimethylamino)pyridine / CH2Cl2 / 4 h / Ambient temperature
With dmap; lithium aluminium tetrahydride; sodium hydride; toluene-4-sulfonic acid; dicyclohexyl-carbodiimide; In tetrahydrofuran; diethyl ether; dichloromethane; benzene;
DOI:10.1039/c39840001423
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