2-Isopropylcyclohexanol

Base Information

• Chemical Name: 2-Isopropylcyclohexanol
• CAS No.: 96-07-1
• Molecular Formula: C9H18 O
• Molecular Weight: 142.241
• Hs Code.: 2906199090
• European Community (EC) Number: 202-474-6
• NSC Number: 2330
• DSSTox Substance ID: DTXSID70914701
• Nikkaji Number: J46.557G
• Mol file: 96-07-1.mol

Synonyms:2-Isopropylcyclohexanol;96-07-1;2-Isopropylcyclohexan-1-ol;2-(propan-2-yl)cyclohexan-1-ol;Cyclohexanol, 2-(1-methylethyl)-;2-propan-2-ylcyclohexan-1-ol;Cyclohexanol, 2-isopropyl-;Cyclohexanol,2-(1-methylethyl)-;EINECS 202-474-6;AI3-17386;NSC2330;SCHEMBL680648;DTXSID70914701;NSC 2330;NSC-2330;MFCD00072217;Cyclohexanol, cis-2-(1-methylethyl);AKOS004903433;AS-60327;Cyclohexanol, 2-(1-methylethyl)-, cis-;CS-0070118;EN300-93002;C77548;A904050;F8889-0707;Z992949104

Chemical Property of 2-Isopropylcyclohexanol

Chemical Property:

• Vapor Pressure: 0.0684mmHg at 25°C
• Boiling Point: 203.1°Cat760mmHg
• Flash Point: 80.8°C
• PSA: 20.23000
• Density: 0.914g/cm³
• LogP: 2.19350
• Storage Temp.: Sealed in dry,Room Temperature
• XLogP3: 2.6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 142.135765193
• Heavy Atom Count: 10
• Complexity: 98.9

Purity/Quality:

97% ^*data from raw suppliers

2-(propan-2-yl)cyclohexan-1-ol ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)C1CCCCC1O

Technology Process of 2-Isopropylcyclohexanol

There total 15 articles about 2-Isopropylcyclohexanol 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:

2-(1-methylethyl)phenol (88-69-7) → 2-Isopropylcyclohexanol (96-07-1)

Guidance literature:

With hydrogen; Ru-carbon; under 77572.2 Torr;

DOI:10.1021/jo00411a026

Reference yield:

→ 2-Isopropylcyclohexanol (96-07-1)

Guidance literature:

2-Isopropylcyclohexanon, Reduktion;

Reference yield:

trans-2-isopropyl-cyclohex-3-enol → (+/-)-trans-2-Isopropyl-cyclohexanol (96-07-1,10488-23-0,10488-25-2,64823-98-9,98043-34-6,98102-89-7,98102-90-0,98102-91-1,98102-92-2)

Guidance literature:

With hydrogen; palladium on activated charcoal; In ethyl acetate;

upstream raw materials:

2-(1-methylethyl)phenol

2-isopropylcyclohexanone

aluminum isopropoxide

cis-2-isopropylcyclohexan-1-ol

Downstream raw materials:

2-isopropylcyclohexanone

2-Isopropyl-1-phenyl-cyclohexanol

6-Isopropyl-1-phenyl-cyclohexen-⁽¹⁾

cis-2-isopropylcyclohexan-1-ol

Refernces

Nucleic acid related compounds. 38. Smooth and high-yield iodination and chlorination at C-5 of uracil bases and p-toluyl-protected nucleosides

10.1139/v82-082

The study investigates the iodination and chlorination of uracil bases and protected nucleosides. Iodine monochloride (ICl) is used to iodinate uracil compounds, yielding 5-iodouracil derivatives with over 95% purified yields. Iodobenzene dichloride (PhICl?) is employed for chlorination, resulting in 5-chlorouracil products. The nucleosides are protected as p-toluyl esters, which enhance their solubility in organic solvents and facilitate high-yield crystallization. The study provides a convenient and efficient method for synthesizing 5-substituted uracil derivatives, which have potential applications in the treatment of neoplastic and viral diseases.

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