4423-47-6 Usage
Description
[1,1':4',1''-Terphenyl]-2',3',5'-triol is a phenolic compound that belongs to the class of trihydroxyflavones. It features a terphenyl backbone with three hydroxyl groups attached, and is commonly found in various plants. This chemical has been investigated for its potential pharmacological properties, such as antioxidant and anti-inflammatory activities, as well as its use in the synthesis of novel organic compounds and the production of polymers with specific properties. Furthermore, it has shown promise in material science for enhancing the thermal and mechanical properties of composites.
Uses
Used in Pharmaceutical Applications:
[1,1':4',1''-Terphenyl]-2',3',5'-triol is used as a potential therapeutic agent for its antioxidant and anti-inflammatory properties, which may contribute to the treatment or management of various diseases and conditions.
Used in Chemical Synthesis:
[1,1':4',1''-Terphenyl]-2',3',5'-triol is used as a building block in the synthesis of novel organic compounds, potentially leading to the development of new pharmaceuticals, agrochemicals, or other specialty chemicals.
Used in Polymer Production:
[1,1':4',1''-Terphenyl]-2',3',5'-triol is used as a component in the production of polymers with specific properties, such as enhanced thermal stability or mechanical strength, for various industrial applications.
Used in Material Science:
[1,1':4',1''-Terphenyl]-2',3',5'-triol is used to enhance the thermal and mechanical properties of composites, making it a valuable additive in the development of advanced materials for various industries, including aerospace, automotive, and electronics.
Used in the Plant Industry:
[1,1':4',1''-Terphenyl]-2',3',5'-triol is used as a natural compound found in various plants, which may have potential applications in the study of plant biochemistry, ecology, or as a source of bioactive compounds for pharmaceutical or agricultural applications.
Check Digit Verification of cas no
The CAS Registry Mumber 4423-47-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,2 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4423-47:
(6*4)+(5*4)+(4*2)+(3*3)+(2*4)+(1*7)=76
76 % 10 = 6
So 4423-47-6 is a valid CAS Registry Number.
4423-47-6Relevant articles and documents
The coupled reaction catalyzed by EchB and EchC lead to the formation of the common 2′,3′,5′-trihydroxy-benzene core in echosides biosynthesis
Zhu, Jing,Liu, Mengyujie,Deng, Jingjing,Chen, Wang,Zhu, Deyu,Duan, Jing,Li, Yaoyao,Wang, Haoxin,Shen, Yuemao
, p. 62 - 69 (2021)
p-Terphenyls represent a unique family of aromatic natural products generated by nonribosomal peptide synthetase-like (NRPS-like) enzyme. After formation of p-terphenyl skeleton, tailoring modifications will give rise to structural diversity and various biological activities. Here we demonstrated a two-enzyme (EchB, a short-chain dehydrogenase/reductase (SDR), and EchC, a nuclear transport factor 2 (NTF2)-like dehydratase) participated transformation from dihydroxybenzoquinone core to 2′,3′,5′-trihydroxy-benzene in the biosynthesis of echosides. Beginning with polyporic acid as substrate, successive steps of reduction-dehydration-reduction cascade catalyzed by EchB-EchC-EchB were concluded after in vivo gene disruption and in vitro bioassay experiments. These findings demonstrated a conserved synthesis pathway of 2′,3′,5′-trihydroxy-p-terphenyls in bacteria, such as Actinomycetes and Burkholderia. The parallel pathway in fungi has yet to be explored.
