53723-50-5 Usage
Description
Cyclohexanol, 2-methylene-, acetate is a chemical compound characterized as a clear, colorless liquid with a sweet, floral odor. It is utilized as a solvent and in the production of fragrances and flavors, playing a significant role in various industries due to its versatile applications.
Uses
Used in Coatings Industry:
Cyclohexanol, 2-methylene-, acetate is used as a solvent for the manufacturing of coatings, contributing to the product's desired consistency and performance.
Used in Inks Industry:
In the inks industry, Cyclohexanol, 2-methylene-, acetate is used as a solvent, aiding in the production of high-quality inks with the appropriate flow and drying properties.
Used in Adhesives Industry:
Cyclohexanol, 2-methylene-, acetate is used as a solvent in the production of adhesives, enhancing their bonding capabilities and overall performance.
Used in Cleaning Products Industry:
As a component in cleaning products, Cyclohexanol, 2-methylene-, acetate is used as a solvent to help dissolve and remove various soils and stains effectively.
Used in Synthetic Resins Production:
Cyclohexanol, 2-methylene-, acetate is used as a solvent in the production of synthetic resins, playing a crucial role in achieving the desired properties of the final product.
Used in Essential Oils Extraction:
This chemical compound is utilized in the extraction of essential oils, where it serves as a solvent to help isolate the desired fragrances and compounds from plant materials.
Used in Plasticizers Production:
Cyclohexanol, 2-methylene-, acetate is used as a plasticizer in the production of vinyl resins and acetate-based varnishes, providing flexibility and durability to the final products.
This chemical is considered to be relatively safe for use in consumer products when handled properly, making it a valuable component in a wide range of applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 53723-50-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,7,2 and 3 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 53723-50:
(7*5)+(6*3)+(5*7)+(4*2)+(3*3)+(2*5)+(1*0)=115
115 % 10 = 5
So 53723-50-5 is a valid CAS Registry Number.
53723-50-5Relevant articles and documents
Lipase-catalyzed kinetic resolution of 2-methylene-substituted cycloalkanols in batch and continuous-flow modes
Tomin, Anna,Hornyánszky, Gábor,Kupai, Katalin,Dorkó, Zsanett,ürge, László,Darvas, Ferenc,Poppe, László
experimental part, p. 859 - 865 (2011/12/15)
Kinetic resolutions of cyclic racemic secondary alcohols (2-methylenecyclopentan-1-ol rac-1a, 2-methylenecyclohexan-1-ol rac-1b, 2-methylenecycloheptan-1-ol rac-1c, 6-methylene-[1,3]dioxepan-5-ol rac-1d, 2,2-dimethyl-6-methylene-[1,3]dioxepan-5-ol rac-1e and trans-2-bromocyclohexan-1-ol rac-3) catalyzed by different (commercial and in-house-made) lipases were performed using vinyl acetate in THF-hexane. In the most typical cases (rac-1b, rac-1d and rac-3), the immobilized Candida antarctica lipase B (CaLB, for rac-1b and rac-3)- or sol-gel immobilized Pseudomonas fluorescens lipase (sol-gel LAK, for rac-1d)-catalyzed batch mode reactions were compared to the continuous mode reactions carried out in an enzyme-filled stainless steel bioreactor. The effect of temperature (20-60 °C) and flow rate (0.1-0.3 ml min-1) on the continuous-flow acetylation of rac-1b, rac-1d and rac-3 were investigated. In the kinetic resolutions of rac-1b, rac-1d and rac-3, the enantiomeric selectivities (E) were similar in the continuous-flow and batch (shake flask) modes. However, the productivities (specific reaction rate: r), were significantly higher in the continuous-flow mode biotransformations of rac-1b, rac-1d and rac-3.
THE NITROGENATED ALLYLIC SYSTEM AS AN INTRAMOLECULAR NUCLEOPHILE: A NEW ROUTE TO PYRAZOLES
Momose, Takefumi,Toyooka, Naoki,Ikuta, Takashi,Yanagino, Hironobu
, p. 789 - 793 (2007/10/02)
A new route to pyrazoles via the cyclization of N-allyl-N-nitrosoamides is described.
The conformational preference of methoxyl and acetoxyl groups in 3-oxycyclohexenes, 2-oxymethylenecyclohexanes, and 1-oxytetralins and the generalized anomeric effect
Ouedraogo, Adama,Viet, Minh Tan Phan,Saunders, John K.,Lessard, Jean
, p. 1761 - 1768 (2007/10/02)
The 13C and 1H nuclear magnetic resonance data of 3-oxycyclohexenes, 2-oxymethylenecyclohexanes, and 1-oxytetralins show (i) that the pseudoaxial preference is larger for the acetoxyl group than for the methoxyl group in 3-oxycyclohexenes, (ii) that the m
