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7-methylheptalactone

Base Information Edit
  • Chemical Name:7-methylheptalactone
  • CAS No.:126372-23-4
  • Molecular Formula:C8H14O2
  • Molecular Weight:142.198
  • Hs Code.:
  • Mol file:126372-23-4.mol
7-methylheptalactone

Synonyms:

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 7-methylheptalactone Edit
Chemical Property:
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Technology Process of 7-methylheptalactone

There total 1 articles about 7-methylheptalactone 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:
cycloheptanone; With lithium diisopropyl amide; In tetrahydrofuran; hexane; at 0 ℃; for 0.5h;
methyl iodide; In tetrahydrofuran; hexane; at -78 ℃;
With 3-chloro-benzenecarboperoxoic acid; In chloroform; for 168000h; Further stages. Title compound not separated from byproducts.;
DOI:10.1021/ja071241a
Guidance literature:
Multi-step reaction with 6 steps
1.1: porcine liver esteraze; NaOH / aq. phosphate buffer / pH 7.2
2.1: carbonyl diimidazole / tetrahydrofuran / 4 h / 0 °C
2.2: 74 percent / tetrahydrofuran / cooling
3.1: 99 percent / [((R)-BINAP)RuCl2]2*NEt3; H2 / methanol; tetrahydrofuran / 15 h / 65 °C / 15001.5 Torr
4.1: molecular sieves 4 Angstroem / CH2Cl2 / 0.5 h / 20 °C
4.2: 82 percent / TMSOTf / CH2Cl2 / 2.5 h / -78 °C
5.1: 82 percent / LiAlH4 / tetrahydrofuran / 1 h / 0 °C
6.1: tri-n-butylphosphine; o-nitrophenyl selenocyanate / tetrahydrofuran / 30 h
6.2: 90 percent / aq. H2O2 / tetrahydrofuran / 0 - 20 °C
With sodium hydroxide; lithium aluminium tetrahydride; ortho-nitrophenyl selenocyanate; tributylphosphine; [((R)-Binap)-RuCl2]2; 4 A molecular sieve; porcine liver esteraze; hydrogen; 1,1'-carbonyldiimidazole; In tetrahydrofuran; methanol; phosphate buffer; dichloromethane;
DOI:10.1021/ja027346p
Guidance literature:
Multi-step reaction with 4 steps
1.1: porcine liver esteraze; NaOH / aq. phosphate buffer / pH 7.2
2.1: carbonyl diimidazole / tetrahydrofuran / 4 h / 0 °C
2.2: 74 percent / tetrahydrofuran / cooling
3.1: 99 percent / [((R)-BINAP)RuCl2]2*NEt3; H2 / methanol; tetrahydrofuran / 15 h / 65 °C / 15001.5 Torr
4.1: molecular sieves 4 Angstroem / CH2Cl2 / 0.5 h / 20 °C
4.2: 82 percent / TMSOTf / CH2Cl2 / 2.5 h / -78 °C
With sodium hydroxide; [((R)-Binap)-RuCl2]2; 4 A molecular sieve; porcine liver esteraze; hydrogen; 1,1'-carbonyldiimidazole; In tetrahydrofuran; methanol; phosphate buffer; dichloromethane;
DOI:10.1021/ja027346p
upstream raw materials:

methyl iodide

cycloheptanone

Downstream raw materials:

<+/->-7-hydroxyoctanoic acid

C64H76O12

C64H78O13

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