5-(1-Hydroxy-1-methylethyl)-2-methyl-2-cyclohexen-1-one, (S)-

Base Information

• Chemical Name: 5-(1-Hydroxy-1-methylethyl)-2-methyl-2-cyclohexen-1-one, (S)-
• CAS No.: 34182-03-1
• Molecular Formula: C10H16O2
• Molecular Weight: 168.236
• DSSTox Substance ID: DTXSID30437981
• Nikkaji Number: J370.412B
• Wikidata: Q82253587
• Mol file: 34182-03-1.mol

Synonyms:D-8-Hydroxycarvotanacetone;5-(1-Hydroxy-1-methylethyl)-2-methyl-2-cyclohexen-1-one, (S)-;(S)-8-Hydroxy-p-menth-1-en-6-one;34182-03-1;SCHEMBL6910673;DTXSID30437981;DJOOMNLGIUGRKD-MRVPVSSYSA-N;(5R)-5-(2-HYDROXYPROPAN-2-YL)-2-METHYLCYCLOHEX-2-EN-1-ONE

Chemical Property of 5-(1-Hydroxy-1-methylethyl)-2-methyl-2-cyclohexen-1-one, (S)-

Chemical Property:

• XLogP3: 1.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 168.115029749
• Heavy Atom Count: 12
• Complexity: 226

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=CCC(CC1=O)C(C)(C)O
• Isomeric SMILES: CC1=CC[C@H](CC1=O)C(C)(C)O

Technology Process of 5-(1-Hydroxy-1-methylethyl)-2-methyl-2-cyclohexen-1-one, (S)-

There total 17 articles about 5-(1-Hydroxy-1-methylethyl)-2-methyl-2-cyclohexen-1-one, (S)- 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:

Reference yield: 98.0%

(4R,6R)-6-hydroxy-4-(1-hydroxyisopropyl)-1-methylcyclohexene (772-36-1) → (R)-5-(1-hydroxy-1-methylethyl)2-methylcyclohex-2-enone (34182-03-1)

Guidance literature:

With N-methyl-2-indolinone; tetrapropylammonium perruthennate; 4 Angstroem sives; In dichloromethane; at 20 ℃; for 2h;

DOI:10.1016/S0957-4166(00)00339-6

Reference yield: 65.0%

trans-sobrerol (38235-58-4) → (+/-)-5-(1-hydroxy-1-methylethyl)-2-methyl-2-cyclohexen-1-one (34182-03-1,67738-03-8,7712-46-1,60593-11-5)

Guidance literature:

With manganese(IV) oxide; In acetone; for 48h;

DOI:10.1002/oms.1210220809

Reference yield: 21.0%

(S)-p-mentha-6,8-dien-2-one (2244-16-8,6485-40-1) → (+/-)-5-(1-hydroxy-1-methylethyl)-2-methyl-2-cyclohexen-1-one (34182-03-1,67738-03-8,7712-46-1,60593-11-5)

Guidance literature:

In water; at 210 ℃; for 0.166667h;

DOI:10.1021/jo962115k

upstream raw materials:

(R)-Carvone

(-)-trans-sobrerol

(-)-2α-Brom-10β-pinan-3-on

(4R,6R)-6-hydroxy-4-(1-hydroxyisopropyl)-1-methylcyclohexene

Downstream raw materials:

8-Hydroxy-p-menthan-2-on

C₁₇H₂₄N₂O₃S

(2S,5R)-5-Isopropenyl-2-methyl-2-pent-4-enyl-cyclohexanone

(2S,5R)-5-Isopropenyl-2-methyl-2-pent-4-ynyl-cyclohexanone