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(R,S)-(2Z,4E)-3-methyl-5-(6-<13CD3>-2,6,6-trimethylcyclohex-1-en-1-yl)-2,4-pentadienenal

Base Information Edit
  • Chemical Name:(R,S)-(2Z,4E)-3-methyl-5-(6-<13CD3>-2,6,6-trimethylcyclohex-1-en-1-yl)-2,4-pentadienenal
  • CAS No.:168416-27-1
  • Molecular Formula:C15H22O
  • Molecular Weight:222.304
  • Hs Code.:
  • Mol file:168416-27-1.mol
(R,S)-(2Z,4E)-3-methyl-5-(6-<13CD3>-2,6,6-trimethylcyclohex-1-en-1-yl)-2,4-pentadienenal

Synonyms:(R,S)-(2Z,4E)-3-methyl-5-(6-<13CD3>-2,6,6-trimethylcyclohex-1-en-1-yl)-2,4-pentadienenal

Suppliers and Price of (R,S)-(2Z,4E)-3-methyl-5-(6-<13CD3>-2,6,6-trimethylcyclohex-1-en-1-yl)-2,4-pentadienenal
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of (R,S)-(2Z,4E)-3-methyl-5-(6-<13CD3>-2,6,6-trimethylcyclohex-1-en-1-yl)-2,4-pentadienenal Edit
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Technology Process of (R,S)-(2Z,4E)-3-methyl-5-(6-<13CD3>-2,6,6-trimethylcyclohex-1-en-1-yl)-2,4-pentadienenal

There total 6 articles about (R,S)-(2Z,4E)-3-methyl-5-(6-<13CD3>-2,6,6-trimethylcyclohex-1-en-1-yl)-2,4-pentadienenal 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:
With hydrogenchloride; In 1,2-dichloro-ethane; at 55 ℃; for 1h;
DOI:10.1002/jlcr.2580360807
Guidance literature:
Multi-step reaction with 3 steps
1: 1.) LDA / 1.) THF, hexane, -78 deg C, 30 min, 2.) THF, hexane, -78 deg C
2: 98 percent / DIBAL / tetrahydrofuran / 0.25 h / -78 °C
3: 86 percent / aq. HCl / 1,2-dichloro-ethane / 1 h / 55 °C
With hydrogenchloride; diisobutylaluminium hydride; lithium diisopropyl amide; In tetrahydrofuran; 1,2-dichloro-ethane;
DOI:10.1002/jlcr.2580360807
Guidance literature:
Multi-step reaction with 5 steps
1: aq. HCl / ethanol / 4 h / 82 °C
2: 1.) n-BuLi, TMEDA / 1.) hexane, a) -78 deg C, 30 min, b) RT, 4 h, 2.) hexane, RT, 12 h
3: 1.) LDA / 1.) THF, hexane, -78 deg C, 30 min, 2.) THF, hexane, -78 deg C
4: 98 percent / DIBAL / tetrahydrofuran / 0.25 h / -78 °C
5: 86 percent / aq. HCl / 1,2-dichloro-ethane / 1 h / 55 °C
With hydrogenchloride; n-butyllithium; N,N,N,N,-tetramethylethylenediamine; diisobutylaluminium hydride; lithium diisopropyl amide; In tetrahydrofuran; ethanol; 1,2-dichloro-ethane;
DOI:10.1002/jlcr.2580360807
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