15356-72-6 Usage
Description
Methyl 3-(2,6,6-trimethylcyclohexen-1-yl)acrylate is a colorless liquid chemical compound with the molecular formula C13H20O2. It has a fruity odor and is commonly used in the synthesis of polymers and resins. This derivative of acrylic acid is often utilized in the production of adhesives, coatings, and other industrial applications. Its unique structure, featuring a cyclohexene ring and an acrylate group, provides it with desirable properties for various chemical reactions and polymerization processes. However, it is important to handle this chemical with care, as it may cause skin and eye irritation upon contact.
Uses
Used in Polymer and Resin Synthesis:
Methyl 3-(2,6,6-trimethylcyclohexen-1-yl)acrylate is used as a monomer in the synthesis of polymers and resins for its unique structure and desirable properties in chemical reactions and polymerization processes.
Used in Adhesive Production:
In the adhesive industry, methyl 3-(2,6,6-trimethylcyclohexen-1-yl)acrylate is used as a component in the formulation of adhesives due to its ability to enhance the bonding properties and durability of the final product.
Used in Coating Formulation:
Methyl 3-(2,6,6-trimethylcyclohexen-1-yl)acrylate is used as an ingredient in coating formulations to improve the performance characteristics such as adhesion, flexibility, and resistance to environmental factors.
Used in Other Industrial Applications:
This chemical compound is also utilized in various other industrial applications where its unique properties can contribute to the development of high-quality products.
Check Digit Verification of cas no
The CAS Registry Mumber 15356-72-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,3,5 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15356-72:
(7*1)+(6*5)+(5*3)+(4*5)+(3*6)+(2*7)+(1*2)=106
106 % 10 = 6
So 15356-72-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H20O2/c1-10-6-5-9-13(2,3)11(10)7-8-12(14)15-4/h7-8H,5-6,9H2,1-4H3/b8-7+
15356-72-6Relevant articles and documents
Photocatalytic e → Z Isomerization of β-Ionyl Derivatives
Livingstone, Keith,Tenberge, Marius,Pape, Felix,Daniliuc, Constantin G.,Jamieson, Craig,Gilmour, Ryan
, p. 9677 - 9680 (2019/11/29)
An operationally simple E → Z isomerization of activated dienes, based on the β-ionyl motif intrinsic to retinal, is reported using inexpensive (-)-riboflavin (vitamin B2) under irradiation at 402 nm. Selective energy transfer from photoexcited (-)-riboflavin to the starting E-isomer enables geometrical isomerization. Since the analogous process with the Z-isomer is inefficient, microscopic reversibility is circumvented, thereby enabling a directional isomerization to generate the contra-thermodynamic product (up to 99% yield, up to 99:1 Z/E). Prudent choice of photocatalyst enables chemoselective isomerization to be achieved in both inter- and intramolecular systems. The principles established from this study, together with a molecular editing approach, have facilitated the development of a regioselective isomerization of a truncated triene based on the retinal scaffold.
OPSIN-BINDING LIGANDS, COMPOSITIONS AND METHODS OF USE
-
, (2010/12/31)
Compounds and compositions of said compounds along with methods of use of compounds are disclosed for treating ophthalmic conditions related to mislocalization of opsin proteins, the misfolding of mutant opsin proteins and the production of toxic visual cycle products that accumulate in the eye. Compounds and compositions useful in the these methods, either alone or in combination with other therapeutic agents, are also described.
Contribution of methyls in retinal side chain to regioselective photoisomerization of retinochromes
Tsujimoto, Kazuo,Sugiura, Jun'ichirou,Takemori, Nobuaki,Mizukami, Taku
, p. 1051 - 1052 (2007/10/03)
All-trans-9-demethyl-11-methylretinal was synthesized to elucidate the chromophoric interaction between hydrophobic part in retinochrome and 9-methyl substituent of retinal. Photoirradiation of its pigment efficiently gave the 11-cis-isomer in 90% regiose
