4-(Propan-2-yl)cyclohex-1-ene-1-carboxylic acid

Base Information

Chemical Name:4-(Propan-2-yl)cyclohex-1-ene-1-carboxylic acid
CAS No.:586-88-9
Molecular Formula:C₁₀H₁₆O₂
Molecular Weight:168.236
Hs Code.:
UNII:1M1X0Z101M
DSSTox Substance ID:DTXSID20486721
Nikkaji Number:J11.507J
Mol file:586-88-9.mol

Synonyms:Phellandric acid;586-88-9;1M1X0Z101M;Phellandric acid , (+/-);UNII-1M1X0Z101M;4-(Propan-2-yl)cyclohex-1-ene-1-carboxylic acid;4-(1-Methylethyl)-1-cyclohexene-1-carboxylic acid;1-Cyclohexene-1-carboxylic acid, 4-(1-methylethyl)-;4-propan-2-ylcyclohexene-1-carboxylic acid;SCHEMBL10705510;DTXSID20486721;PHELLANDRIC ACID , (+/-)-

Suppliers and Price of 4-(Propan-2-yl)cyclohex-1-ene-1-carboxylic acid

Supply Marketing:

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

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Chemical Property of 4-(Propan-2-yl)cyclohex-1-ene-1-carboxylic acid

Chemical Property:

PSA：37.30000
LogP:2.45350
XLogP3:2.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:168.115029749
Heavy Atom Count:12
Complexity:204

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)C1CCC(=CC1)C(=O)O

Technology Process of 4-(Propan-2-yl)cyclohex-1-ene-1-carboxylic acid

There total 6 articles about 4-(Propan-2-yl)cyclohex-1-ene-1-carboxylic acid 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:

: 586-88-9
4-isopropylcyclohex-1-en-7-oic acid

Guidance literature:: With potassium hydroxide; Erwaermen des erhaltenen Saeuregemisches mit Natriumaethylat in Aethanol;
DOI:10.1021/ja01180a005