37797-30-1 Usage
Description
[(E)-diazene-1,2-diyldibenzene-4,1-diyl]dimethanol, also known as 4,4'-methylenedibenzene-1,2-diol, is a complex chemical compound that features a diol structure with benzene and methanol groups. [(E)-diazene-1,2-diyldibenzene-4,1-diyl]dimethanol is characterized by the presence of two hydroxyl (OH) functional groups, which provide it with a high degree of reactivity and versatility in organic synthesis. Its unique structure and functional groups may endow it with potential applications across various fields, including pharmaceuticals, dyes, and materials science.
Uses
Used in Pharmaceutical Industry:
[(E)-diazene-1,2-diyldibenzene-4,1-diyl]dimethanol is used as a building block in the pharmaceutical industry for the synthesis of complex organic molecules and polymers. Its unique structure and functional groups can be leveraged to create new drugs with specific therapeutic properties.
Used in Dyes Industry:
In the dyes industry, [(E)-diazene-1,2-diyldibenzene-4,1-diyl]dimethanol is used as a precursor for the development of novel dyes with improved colorfastness and stability. Its benzene and methanol groups can be manipulated to produce dyes with specific color characteristics and applications.
Used in Materials Science:
[(E)-diazene-1,2-diyldibenzene-4,1-diyl]dimethanol is utilized in materials science for the synthesis of advanced materials with unique properties. Its diol structure and functional groups can contribute to the development of new polymers, coatings, and composites with enhanced performance characteristics.
As a Precursor in Chemical Research and Development:
[(E)-diazene-1,2-diyldibenzene-4,1-diyl]dimethanol serves as a valuable precursor in chemical research and development, enabling the synthesis of more complex molecules and polymers. Its potential applications in various industries can be further explored through continued research and experimentation.
Check Digit Verification of cas no
The CAS Registry Mumber 37797-30-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,7,9 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 37797-30:
(7*3)+(6*7)+(5*7)+(4*9)+(3*7)+(2*3)+(1*0)=161
161 % 10 = 1
So 37797-30-1 is a valid CAS Registry Number.
37797-30-1Relevant articles and documents
Azobenzene-Based Macrocyclic Arenes: Synthesis, Crystal Structures, and Light-Controlled Molecular Encapsulation and Release
Liu, Yuezhou,Wang, Hongliang,Liu, Peiren,Zhu, Huangtianzhi,Shi, Bingbing,Hong, Xin,Huang, Feihe
, p. 5766 - 5770 (2021)
Azobenzene (azo)-based macrocycles are highly fascinating in supramolecular chemistry because of their light-responsiveness. In this work, a series of azo-based macrocyclic arenes 1, 2, 3, and 4, distinguished by the substituted positions of azo groups, i
A Paclitaxel Prodrug Activatable by Irradiation in a Hypoxic Microenvironment
Chen, Guang,Hu, Xiuli,Jing, Xiabin,Liu, Shi,Pei, Qing,Xia, Rui,Xie, Zhigang,Zhou, Shiyu
, p. 23198 - 23205 (2020)
The innate hypoxic microenvironment of most solid tumors has a major influence on tumor growth, invasiveness, and distant metastasis. Here, a hypoxia-activated self-immolative prodrug of paclitaxel (PTX2-Azo) was synthesized and encapsulated by
Palladium Nanoparticles on Silica Nanospheres for Switchable Reductive Coupling of Nitroarenes
Lakshminarayana, Bhairi,Manna, Arun Kumar,Satyanarayana,Subrahmanyam, Ch.
, p. 2309 - 2321 (2020/02/18)
Abstract: In this study, we synthesized a robust and sustainable Pd/SiO2 nanospheres catalyst. Further, its catalytic activity was demonstrated for the direct reductive coupling of nitroarenes under mild conditions. While the reaction with Pd nanoparticles on other supporting materials such as modified carbon materials and TiO2, under similar conditions, resulted formation of amines exclusively. Therefore, it was confirmed that the SiO2 was found to be the best supporting material towards the selective reductive coupling of nitroarenes. Also, the catalyst could be recycled up to five cycles with a marginal loss of product yield ( 2% yield). Graphic Abstract: [Figure not available: see fulltext.].
System and method for reversible photo-controlled gene silencing
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Page/Page column 4; 21; 22, (2020/08/07)
In one aspect, a chemically-modified siRNA for reversible photo-controlled gene silencing is provided. In one embodiment, one or more nucleotides the sense strand of the siRNA are replaced with a spacer comprising an azobenzene or derivative thereof. The
