351435-98-8 Usage
Uses
Used in Polymer and Resin Manufacturing:
(Benzene-1,3,5-triyl)tris(3-phenylacrylonitrile) is used as a key component in the manufacturing of polymers and resins. Its stability and structural properties contribute to the development of high-quality materials with specific characteristics, such as strength and durability.
Used in Organic Synthesis:
(benzene-1,3,5-triyl)tris(3-phenylacrylonitrile) serves as a building block in the synthesis of various organic compounds. Its unique structure allows for the creation of a wide range of molecules with different properties and applications.
Used in Industrial Applications:
(Benzene-1,3,5-triyl)tris(3-phenylacrylonitrile) is utilized in various industrial applications due to its stability and chemical properties. Its versatility in organic synthesis and polymer manufacturing makes it a valuable compound for creating materials with specific characteristics for different industries.
Safety Precautions:
It is important to handle (benzene-1,3,5-triyl)tris(3-phenylacrylonitrile) with care, as it can be toxic if ingested, inhaled, or comes into contact with skin or eyes. Proper safety measures should be taken to minimize the risk of exposure and ensure the safe use of (benzene-1,3,5-triyl)tris(3-phenylacrylonitrile) in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 351435-98-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,1,4,3 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 351435-98:
(8*3)+(7*5)+(6*1)+(5*4)+(4*3)+(3*5)+(2*9)+(1*8)=138
138 % 10 = 8
So 351435-98-8 is a valid CAS Registry Number.
351435-98-8Relevant academic research and scientific papers
Lim, Yoonbin,Choi, Insil,Lee, Hyunpyo,Kim, Il Won,Chang, Ji Young
, p. 5963 - 5968 (2014)
The piezochromic behaviours of C3-symmetric molecules with p-bromophenyl side groups connected to a phenyl ring core through cyano-vinylene bridges were studied. Upon grinding, α-BPAN-Br having cyano groups at the α-position to the phenyl ring core exhibited substantial quenching of a bluish green emission (on-off switching) and its constitutional isomer, β-BPAN-Br, showed an emission colour change from bluish green to deep blue (colour tuning). When the molecules were exposed to an organic vapour, the initial emission of each molecule was restored. The powder X-ray diffraction and DSC studies revealed that the as-synthesized and vapour-annealed samples had the same crystalline structures, while the ground samples had amorphous structures. Their structural analogues, α-BPAN-H and β-BPAN-H which had no bromo groups, did not show any piezochromic or vapochromic behaviour. Poly(β-BPAN) consisting of covalently linked β-BPAN units were prepared by Ullmann reaction of β-BPAN-Br. The polymer showed similar luminescence to that of crystalline β-BPAN-Br, but its initial emission was not changed by grinding. the Partner Organisations 2014.
