115595-27-2 Usage
Description
4-(3-Butenyloxy)benzoic Acid, a chemical compound with the molecular formula C11H12O3, is an organic compound that features a benzoic acid core with a butenyloxy group attached to the para position. This structure endows it with unique chemical and physical properties, making it a versatile building block in various applications.
Uses
Used in Polymer Synthesis:
4-(3-Butenyloxy)benzoic Acid is used as a reactant in the synthesis of monodomain liquid crystalline elastomers. These elastomers are a type of advanced polymer material that exhibits unique mechanical and optical properties due to their liquid crystalline nature. The incorporation of 4-(3-Butenyloxy)benzoic Acid into the polymer structure contributes to the formation of these properties, making it a valuable component in the development of high-performance materials for various applications.
Used in Chemical Industry:
In the chemical industry, 4-(3-Butenyloxy)benzoic Acid can be utilized as an intermediate for the production of various specialty chemicals, such as pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure allows for further functionalization and modification, enabling the synthesis of a wide range of compounds with specific properties and applications.
Used in Research and Development:
4-(3-Butenyloxy)benzoic Acid can also be employed as a research tool in the development of new materials and chemical processes. Its unique structure and reactivity make it an interesting candidate for studying various chemical reactions and mechanisms, as well as for exploring new applications in different fields.
Check Digit Verification of cas no
The CAS Registry Mumber 115595-27-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,5,9 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 115595-27:
(8*1)+(7*1)+(6*5)+(5*5)+(4*9)+(3*5)+(2*2)+(1*7)=132
132 % 10 = 2
So 115595-27-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H12O3/c1-2-3-8-14-10-6-4-9(5-7-10)11(12)13/h2,4-7H,1,3,8H2,(H,12,13)
115595-27-2Relevant articles and documents
Nickel-catalyzed removal of alkene protecting group of phenols, alcohols via chain walking process
Meng, Chenkai,Niu, Haolin,Ning, Juehan,Wu, Wengang,Yi, Jun
supporting information, (2020/02/04)
An efficient nickel-catalyzed removal of alkene protection group under mild condition with high functional group tolerance through chain walking process has been established. Not only phenolic ethers, but also alcoholic ethers can be tolerated with the retention of stereocenter adjacent to hydroxyl group. The new reaction brings the homoallyl group into a start of new type of protecting group.
SILANE COMPOUND AND POLYMER THEREOF, AND LIQUID CRYSTAL ALIGNMENT LAYER COMPRISING THE POLYMER
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, (2018/11/22)
PROBLEM TO BE SOLVED: To provide a liquid crystal alignment layer that excels in controlling alignment and a pretilt angle of a liquid crystal and has a high voltage holding rate (VHR) as well as a low residual voltage (RDC), a polymer used for the liquid
SHAPE MEMORY MAIN-CHAIN SMECTIC-C ELASTOMERS
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Page/Page column 9, (2009/10/01)
Shape memory main-chain smectic-C elastomers are described, as are methods for their preparation and monomers used in such methods. The elastomers are prepared by hydrosilylation of a reaction mixture including a liquid crystalline diene, a crosslinking agent, and a bis(silyl hydride) compound. The elastomers exhibit shape-memory properties and spontaneously reversible shape changes. They are useful for fabrication of shape memory articles including, for example, implantable medical devices, contact lenses, reversible embossing media, and Fresnel lenses.