6308-92-5

Basic information

• Product Name: 4-Benzoyloxycyclohexanol
• Synonyms: 4-Benzoyloxycyclohexanol;NSC42297;4-hydroxycyclohexyl benzoate;1,4-CYCLOHEXANEDIOL, 1-BENZOATE
• CAS NO: 6308-92-5
• Molecular Formula: C₁₃H₁₆O₃
• Molecular Weight: 220.26434
• Mol File: 6308-92-5.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 346.1°C at 760 mmHg
• Flash Point: 145°C
• Appearance: /
• Density: 1.16g/cm³
• Vapor Pressure: 2.24E-05mmHg at 25°C
• Refractive Index: 1.554
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 4-Benzoyloxycyclohexanol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Benzoyloxycyclohexanol(6308-92-5)
• EPA Substance Registry System: 4-Benzoyloxycyclohexanol(6308-92-5)

Safety Data

• Hazardous Substances Data: 6308-92-5(Hazardous Substances Data)

Usage

General Description

4-Benzoyloxycyclohexanol, also known as p-menthane-3,8-diol, is a chemical compound with the molecular formula C14H20O2. It is a derivative of cyclohexanol and benzoyl chloride. 4-Benzoyloxycyclohexanol has a wide range of applications, including its use as an insect repellent, fragrance ingredient, and flavoring agent. Its insect repellent properties make it popular in products such as mosquito repellents and antiseptics, and it is also used in various personal care and cosmetic products. Additionally, 4-Benzoyloxycyclohexanol has been studied for its potential therapeutic applications, such as antimicrobial and anti-inflammatory properties.

InChI:InChI=1/C13H16O3/c14-11-6-8-12(9-7-11)16-13(15)10-4-2-1-3-5-10/h1-5,11-12,14H,6-9H2

Upstream product

• 556-48-9 1,4-Cyclohexanediol 
• 98-88-4 benzoyl chloride 
• 6995-79-5 cyclohexane-1,4-diol 
• 69558-44-7 trans-4-acetoxy-1-cyclohexanol 
• 2412-73-9 benzoic acid cyclohexyl ester 
• 123-31-9 hydroquinone 
• 108-93-0 cyclohexanol 
• 23510-95-4 4-benzoyloxycyclohexanone 
• 931-71-5 cis-1,4-cyclohexanediol 

Downstream Products

• 23510-95-4 4-benzoyloxycyclohexanone 
• 845507-66-6 cis-4-(toluene-sulfonyl-⁽⁴⁾-oxy)-1-benzoyloxy-cyclohexane 
• 878809-02-0 6-benzoyloxy-3,4,4a,5,6,7,8,8a-octahydro-2(1H)-quinolinone 
• 93-58-3 benzoic acid methyl ester 
• 22428-86-0 4,4-<1,2-ethanediylbis(thio)>cyclohexanol 
• 54531-77-0 4,4-<1,2-ethanediylbis(thio)>cyclohexyl benzoate 
• 83638-29-3 1,4-bis(3,5-dimethoxyphenyl)butane 
• 54531-74-7 4,4-<1,2-ethanediylbis(thio)>cyclohexanone 
• 1071011-29-4 4-fluorocyclohex-3-en-1-yl benzoate 
• 1450812-66-4 C₁₃H₁₃BrO₂ 
• 1450812-67-5 C₆H₉BrO 
• 1450812-68-6 C₈H₁₁BrO₂ 
• 1450812-70-0 C₂₂H₂₁NO₂ 
• 32202-87-2 C₁₉H₁₉NO 

Relevant articles and documents

Synthetic method for cis-1,4-cyclohexanediol

The invention discloses a synthetic method for cis-1,4-cyclohexanediol, belonging to the field of organic chemical synthesis. According to the method, 4-(alkylacyloxy)cyclohexanone is used as a raw material and is only subjected to reduction and hydrolysis so as to conveniently synthesize cis-1,4-cyclohexanediol. The method can guarantee high selectivity of the reactions, and is high in the yieldof cis-1,4-cyclohexanediol and suitable for large-scale production.

Formation of enehydrazine intermediates through coupling of phenylhydrazines with vinyl halides: Entry into the Fischer indole synthesis

Cut to the chase: Direct formation of an enehydrazine, an intermediate in the classic Fischer indole synthesis, solves the regioselectivity problem associated with indolization. This approach not only achieves selective synthesis of indoles through proper selection of the vinyl halide, but also leads to quick construction of desoxyeseroline and esermethole, as well as the key structural motif in the Akuammiline alkaloid vincorine. Copyright

CATALYTIC RADIOFLUORINATION

One aspect of the present invention relates to a method of preparing radio fluorinated substituted alkyl, cycloalkyl, aryl, and alkenyl compounds. In a preferred embodiment, potassium fluoride-18 is used. Another aspect of the invention relates to arylammonium compounds containing fluorine-18 that are useful as imaging agents. In certain embodiments, the ammonium compound is a tetraaryl ammonium salt. Another aspect of the invention relates to arylsulfonium compounds containing fluorine-18 that are useful as imaging agents. In certain embodiments, the sulfonium compound is a triaryl sulfonium salt. Another aspect of the present invention relates to a method of obtaining a positron emission image of a mammal, comprising the steps of administering to a mammal a compound of the invention, and acquiring a positron emission spectrum of the mammal.