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((1S,2S)-2-[1,3]Dioxolan-2-yl-2,6,6-trimethyl-cyclohexyl)-acetaldehyde

Base Information
  • Chemical Name:((1S,2S)-2-[1,3]Dioxolan-2-yl-2,6,6-trimethyl-cyclohexyl)-acetaldehyde
  • CAS No.:97855-72-6
  • Molecular Formula:C14H24O3
  • Molecular Weight:240.343
  • Hs Code.:
((1S,2S)-2-[1,3]Dioxolan-2-yl-2,6,6-trimethyl-cyclohexyl)-acetaldehyde

Synonyms:

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Chemical Property of ((1S,2S)-2-[1,3]Dioxolan-2-yl-2,6,6-trimethyl-cyclohexyl)-acetaldehyde
Chemical Property:
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Technology Process of ((1S,2S)-2-[1,3]Dioxolan-2-yl-2,6,6-trimethyl-cyclohexyl)-acetaldehyde

There total 13 articles about ((1S,2S)-2-[1,3]Dioxolan-2-yl-2,6,6-trimethyl-cyclohexyl)-acetaldehyde 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 12 steps
1: 95 percent / H2 / Adam's catalyst / acetic acid
2: 90 percent / Florisil, PCC / CH2Cl2 / 2 h / Ambient temperature
3: 97 percent / PBB / acetic acid / 2 h / Ambient temperature
4: 97 percent / sodium hydroxide / dimethylformamide; H2O / 0.5 h / Ambient temperature
5: lead tetra-acetate (LTA) / benzene / 0.17 h / Ambient temperature
6: NaBH4 / methanol / 0.33 h / Ambient temperature
7: 98 percent / tributylphosphine / tetrahydrofuran / 0.33 h / Ambient temperature
8: 91 percent / hydrogen peroxide / tetrahydrofuran / 10 h / Ambient temperature
9: 1.) lithium aluminium hydride; 2.) sodium hydroxide / 1.) diethyl ether, rt, 30 min; 2.) water, 30 min.
10: 88 percent / Florisil, PCC / CH2Cl2 / 1 h / Ambient temperature
11: 98 percent / toluene-p-sulphonic acid / benzene / 0.33 h / Heating
12: 1. osmium tetraoxide; 2.) sodium periodate / 1.) diethyl ether, water, rt, 5 min; 2.) rt, 10 h.
With lead(IV) acetate; sodium hydroxide; sodium tetrahydroborate; florisil; sodium periodate; osmium(VIII) oxide; lithium aluminium tetrahydride; tributylphosphine; hydrogen; dihydrogen peroxide; toluene-4-sulfonic acid; pyridinium chlorochromate; platinum(IV) oxide; In tetrahydrofuran; methanol; dichloromethane; water; acetic acid; N,N-dimethyl-formamide; benzene;
Guidance literature:
Multi-step reaction with 13 steps
1: 93 percent / potassium hydroxide, hydrazine hydrate / bis-(2-hydroxy-ethyl) ether / 6 h / Heating
2: 95 percent / H2 / Adam's catalyst / acetic acid
3: 90 percent / Florisil, PCC / CH2Cl2 / 2 h / Ambient temperature
4: 97 percent / PBB / acetic acid / 2 h / Ambient temperature
5: 97 percent / sodium hydroxide / dimethylformamide; H2O / 0.5 h / Ambient temperature
6: lead tetra-acetate (LTA) / benzene / 0.17 h / Ambient temperature
7: NaBH4 / methanol / 0.33 h / Ambient temperature
8: 98 percent / tributylphosphine / tetrahydrofuran / 0.33 h / Ambient temperature
9: 91 percent / hydrogen peroxide / tetrahydrofuran / 10 h / Ambient temperature
10: 1.) lithium aluminium hydride; 2.) sodium hydroxide / 1.) diethyl ether, rt, 30 min; 2.) water, 30 min.
11: 88 percent / Florisil, PCC / CH2Cl2 / 1 h / Ambient temperature
12: 98 percent / toluene-p-sulphonic acid / benzene / 0.33 h / Heating
13: 1. osmium tetraoxide; 2.) sodium periodate / 1.) diethyl ether, water, rt, 5 min; 2.) rt, 10 h.
With lead(IV) acetate; potassium hydroxide; sodium hydroxide; sodium tetrahydroborate; florisil; sodium periodate; osmium(VIII) oxide; lithium aluminium tetrahydride; tributylphosphine; hydrogen; dihydrogen peroxide; toluene-4-sulfonic acid; hydrazine hydrate; pyridinium chlorochromate; platinum(IV) oxide; In tetrahydrofuran; methanol; dichloromethane; water; acetic acid; N,N-dimethyl-formamide; diethylene glycol; benzene;
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