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ethyl 3-allyl-4-benzyloxy-6,8-dimethoxynaphthalene-2-carboxylate

Base Information Edit
  • Chemical Name:ethyl 3-allyl-4-benzyloxy-6,8-dimethoxynaphthalene-2-carboxylate
  • CAS No.:777079-87-5
  • Molecular Formula:C25H26O5
  • Molecular Weight:406.478
  • Hs Code.:
  • Mol file:777079-87-5.mol
ethyl 3-allyl-4-benzyloxy-6,8-dimethoxynaphthalene-2-carboxylate

Synonyms:ethyl 3-allyl-4-benzyloxy-6,8-dimethoxynaphthalene-2-carboxylate

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Chemical Property of ethyl 3-allyl-4-benzyloxy-6,8-dimethoxynaphthalene-2-carboxylate Edit
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Technology Process of ethyl 3-allyl-4-benzyloxy-6,8-dimethoxynaphthalene-2-carboxylate

There total 6 articles about ethyl 3-allyl-4-benzyloxy-6,8-dimethoxynaphthalene-2-carboxylate 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 4 steps
1: 95 percent / guanidine hydrochloride; t-BuOK / ethanol; CH2Cl2 / 1.5 h / 20 °C
2: 99 percent / K2CO3 / acetone / 16 h / Heating
3: 75 percent / dimethylformamide / 12 h / 170 °C
4: 100 percent / K2CO3; KI / acetone / 18 h / Heating
With potassium tert-butylate; guanidine hydrochloride; potassium carbonate; potassium iodide; In ethanol; dichloromethane; N,N-dimethyl-formamide; acetone; 3: Claisen rearrangement;
DOI:10.1039/b407208a
Guidance literature:
Multi-step reaction with 6 steps
1: t-BuOK / 2-methyl-propan-2-ol / 2 h / Heating
2: 8.10 g / sodium acetate / 2 h / 140 °C
3: 95 percent / guanidine hydrochloride; t-BuOK / ethanol; CH2Cl2 / 1.5 h / 20 °C
4: 99 percent / K2CO3 / acetone / 16 h / Heating
5: 75 percent / dimethylformamide / 12 h / 170 °C
6: 100 percent / K2CO3; KI / acetone / 18 h / Heating
With potassium tert-butylate; guanidine hydrochloride; sodium acetate; potassium carbonate; potassium iodide; In ethanol; dichloromethane; N,N-dimethyl-formamide; acetone; tert-butyl alcohol; 1: Stobbe condensation / 5: Claisen rearrangement;
DOI:10.1039/b407208a
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