4727-17-7

Basic information

• Product Name: CYCLOPENTADECANOL
• Synonyms: HYDROXYCYCLOPENTADECANE;CYCLOPENTADECANOL;cyclopentadecan-1-ol;Normuscol
• CAS NO: 4727-17-7
• Molecular Formula: C₁₅H₃₀O
• Molecular Weight: 226.4
• EINECS: 225-221-1
• Mol File: 4727-17-7.mol
• Article Data: 10

Chemical Properties

• Melting Point: 85 °C
• Boiling Point: 328.03°C (rough estimate)
• Flash Point: 140.4°C
• Appearance: /
• Density: 0,93 g/cm3
• Vapor Pressure: 9.83E-06mmHg at 25°C
• Refractive Index: 1.4555 (estimate)
• PKA: 15.36±0.20(Predicted)
• CAS DataBase Reference: CYCLOPENTADECANOL(CAS DataBase Reference)
• NIST Chemistry Reference: CYCLOPENTADECANOL(4727-17-7)
• EPA Substance Registry System: CYCLOPENTADECANOL(4727-17-7)

Safety Data

• TSCA: Yes
• Hazardous Substances Data: 4727-17-7(Hazardous Substances Data)

Usage

General Description

Cyclopentadecanol is a long chain alcohol containing 15 carbon atoms arranged in a cyclopentane ring structure. It is a white, waxy solid with a faint odor, and is insoluble in water but soluble in alcohol and ether. Cyclopentadecanol is commonly used in the production of detergents, lubricants, and as an intermediate in the synthesis of other chemicals. It also has potential applications in the manufacturing of cosmetics, pharmaceuticals, and surfactants. Although it is not considered to be highly toxic, prolonged exposure to high concentrations of cyclopentadecanol may cause irritation to the skin, eyes, and respiratory system. Overall, cyclopentadecanol is a versatile chemical with a range of industrial and commercial uses.

InChI:InChI=1/C15H30O/c16-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-15/h15-16H,1-14H2

Upstream product

• 287-08-1 cis-1,2-epoxycyclopentadecane 
• 502-72-7 cyclopentadecanone 
• 64-17-5 ethanol 
• 60-29-7 diethyl ether 
• 7732-18-5 water 
• 295-48-7 cyclopentadecane 
• 524-38-9 N-hydroxyphthalimide 
• 22591-33-9 acetic acid cyclopentadecyl ester 
• 98348-19-7 2-Acetoxy-cyclopentadecanon-⁽¹⁾ 
• 4727-18-8 2-hydroxycyclopentadecanone 

Downstream Products

• 502-72-7 cyclopentadecanone 
• 6573-72-4 cyclopentadecene 
• 22591-33-9 acetic acid cyclopentadecyl ester 
• 1259516-71-6 cyclopentadecyl 2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside 
• 1259516-70-5 cyclopentadecyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranoside 
• 14224-81-8 cyclopentadecanone 2,4-dinitrophenylhydrazone 
• 1460-18-0 pentadecanedioic acid 
• 502-41-0 cycloheptanol 

Relevant articles and documents

Synthesis of α-Cyclooctyl- and α-Cyclopentadecylglycosides of N-Acetylmuramyl-L-Alanyl-D-Isoglutamine

N-Acetylmuramyl-L-alanyl-D-isoglutamine α-cyclooctyl- and α-cyclopentadecylglycosides were synthesized. The starting peracetylated α-N-glucosaminides were synthesized by reacting the cycloalkanols with peracetyl α-D-glucosaminyl chloride in the presence of Hg(II) iodide in CH3NO2 with heating or by using ZnCl2/tetrabutylammonium bromide in CH2Cl2 at room temperature. Sequential deacetylation, isopropyl protection, and alkylation by (S)-2-bromopropanoic acid gave α-cycloalkyl-4,6-O-isopropylidene-N-acetyl-D-muramic acids, condensation of which with the benzyl ester of L-Ala-D-iGln using the HOSu/DCC method and deprotection afforded the target glycopeptides.

Pincerlike molybdenum complex and preparation method thereof, catalytic composition and application thereof, and alcohol preparation method

The invention discloses a clamp-type molybdenum complex, a preparation method, a corresponding catalyst composition and application. The method comprises the steps: obtaining 9 molybdenum complexes with different structures through coordination reaction of 2-(substituent ethyl)-(5, 6, 7, 8-tetrahydroquinolyl) amine and a corresponding carbonyl molybdenum metal precursor; and catalyzing a ketone compound transfer hydrogenation reaction through a molybdenum complex to generate 40 alcohol compounds. The preparation method of the molybdenum complex is simple, high in yield and good in stability. For a transfer hydrogenation reaction of ketone, the molybdenum-based catalytic system has high catalytic activity and small molybdenum loading capacity, is used for production of aromatic and aliphatic alcohols, and has the advantages of simple method, small environmental pollution and high yield.

Synthesis of β-cycloalkylglycosides of Muramyl Dipeptide

β-Cyclooctyl-, β-cyclodecyl-, and β-cyclopentadecylglycosides of N-acetylmuramyl-L-alanyl-D-isoglutamine were prepared in yields of 39, 18, and 25%, respectively, (calculated for muramic acid) via the reaction of β-cycloalkyl-4,6-O-isopropylidene-N-acetyl-D-muramic acids with the benzyl ester of L-Ala-D-iGln using the HOSu/DCC method followed by deprotection.