74008-14-3 Usage
Uses
Given the provided materials, the potential uses of 2,5-bis(4-methoxyphenyl)[1,3]thiazolo[5,4-d][1,3]thiazole can be hypothesized as follows:
Used in Pharmaceutical Industry:
2,5-bis(4-methoxyphenyl)[1,3]thiazolo[5,4-d][1,3]thiazole is used as a potential drug candidate for its possible biological activities, such as anti-inflammatory, antibacterial, and antitumor properties, which are common among thiazole derivatives.
Used in Materials Science:
2,5-bis(4-methoxyphenyl)[1,3]thiazolo[5,4-d][1,3]thiazole may be utilized in materials science applications due to its unique chemical structure, which could offer novel properties for the development of new materials.
Check Digit Verification of cas no
The CAS Registry Mumber 74008-14-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,0,0 and 8 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 74008-14:
(7*7)+(6*4)+(5*0)+(4*0)+(3*8)+(2*1)+(1*4)=103
103 % 10 = 3
So 74008-14-3 is a valid CAS Registry Number.
74008-14-3Relevant academic research and scientific papers
Synthesis, physical properties and field-effect transistors of novel thiazolothiazole-phenylene co-oligomers
Ando, Shinji,Kumaki, Daisuke,Nishida, Jun-Ichi,Tada, Hirokazu,Inoue, Youji,Tokito, Shizuo,Yamashita, Yoshiro
, p. 553 - 558 (2008/02/05)
A series of thiazolothiazole-phenylene co-oligomers was synthesized and their properties, particularly as semiconductors for OFETs, were investigated. The naphthyl and biphenyl- substituted derivatives showed p-type semiconducting behavior with hole mobilities ranging from 10-2 to 10-1 cm2 V-1 s-1. The hole mobility and on/off ratio were enhanced to 0.12 cm2 V-1 s-1 and 10 6 on the HMDS treated substrate. The introduction of phenyl groups as end substituents was found to be favorable for charge transport and air-stability. The Royal Society of Chemistry 2007.
