97336-76-0 Usage
Molecular structure
Two benzene rings linked by a double bond
Chemical compound
1,1'-Biphenyl, 4-[2-phenyl-1-(phenylmethyl)ethenyl]-, (E)-
Usage
Building block in the synthesis of various organic compounds
Applications
Dyes, pharmaceuticals, and polymers
Role
Important intermediate in the production of fluorescent dyes and optical brighteners
Therapeutic potential
Anti-inflammatory and antioxidant properties
Investigated for
Photosensitive component in photoinitiators and photopolymer materials
Industrial and scientific applications
Versatile and valuable
Check Digit Verification of cas no
The CAS Registry Mumber 97336-76-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,3,3 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 97336-76:
(7*9)+(6*7)+(5*3)+(4*3)+(3*6)+(2*7)+(1*6)=170
170 % 10 = 0
So 97336-76-0 is a valid CAS Registry Number.
97336-76-0Relevant academic research and scientific papers
Carbanion Photochemistry. 8 Effect of Substituent Reduction Potential on the Ground- and Excited-State Isomerization of 2-Aryl-1,3-diphenylpropenyl Anions.
Tolbert, Laren M.,Ali, M. Zaki
, p. 3288 - 3295 (2007/10/02)
The ground- and excited-state chemistry of 2-aryl-1,3-diphenylpropenyl anions is readily described by a Hueckel model.Because of the antisymmetric nonbonding molecular orbital, in the ground state none of the charge is distributed in the central ring.In the excited state, a nonbonding electron is promoted to a symmetric orbital which is localized on the central aryl ring.Thus lowering the reduction potential of the substituent stabilizes the excited state toward electron-transfer-initiated isomerization of cis-stilbene.Conversely, the more stabilized excited states undergo more efficient E,Z isomerization.Finally, if the central substituent is a 4-chlorophenyl group, photoinduced chloride elimination occurs.
