(1R,2S,5R)-2-Isopropyl-5-methylcyclohexyl (2E)-2-butenoate

Base Information Edit

Chemical Name:(1R,2S,5R)-2-Isopropyl-5-methylcyclohexyl (2E)-2-butenoate
CAS No.:66212-46-2
Molecular Formula:C₁₄H₂₄O₂
Molecular Weight:224.343
Hs Code.:
DSSTox Substance ID:DTXSID401170331
Nikkaji Number:J475.322D,J623.135G
Mol file:66212-46-2.mol

Synonyms:DTXSID401170331;(1R,2S,5R)-2-ISOPROPYL-5-METHYLCYCLOHEXYL (2E)-2-BUTENOATE;66212-46-2;(1R,2S,5R)-5-Methyl-2-(1-methylethyl)cyclohexyl (2E)-2-butenoate

Suppliers and Price of (1R,2S,5R)-2-Isopropyl-5-methylcyclohexyl (2E)-2-butenoate

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of (1R,2S,5R)-2-Isopropyl-5-methylcyclohexyl (2E)-2-butenoate Edit

Chemical Property:

XLogP3:4.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:224.177630004
Heavy Atom Count:16
Complexity:256

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC=CC(=O)OC1CC(CCC1C(C)C)C
Isomeric SMILES:C/C=C/C(=O)O[C@@H]1C[C@@H](CC[C@H]1C(C)C)C

Technology Process of (1R,2S,5R)-2-Isopropyl-5-methylcyclohexyl (2E)-2-butenoate

There total 7 articles about (1R,2S,5R)-2-Isopropyl-5-methylcyclohexyl (2E)-2-butenoate 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: 45.0%

: 3724-65-0
2-butenoic acid

: 2216-51-5
(-)-menthol

: 66212-46-2
(1R,2S,5R)-L-menthyl crotonate

: (2E)-N-cyclohexyl-N'-(cyclohexylcarbamoyl)-but-2-enamide

Guidance literature:: With dmap; dicyclohexyl-carbodiimide; In dichloromethane; acetonitrile; at 20 ℃; for 24h; Inert atmosphere;
DOI:10.1039/c4ra15975f