113036-44-5 Usage
Uses
Used in Organic Synthesis:
2,4-Cyclohexadien-1-one, 6-(1,3-dihydro-1,3-dimethyl-2H-benzimidazol-2-ylidene)is used as a building block in organic synthesis for the creation of various complex organic molecules. Its unique structure and functional groups make it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2,4-Cyclohexadien-1-one, 6-(1,3-dihydro-1,3-dimethyl-2H-benzimidazol-2-ylidene)is used as a potential lead compound for the development of new drugs. Its chemical structure can be modified to explore its therapeutic potential against various diseases and disorders. 2,4-Cyclohexadien-1-one,
6-(1,3-dihydro-1,3-dimethyl-2H-benzimidazol-2-ylidene)-'s ability to interact with biological targets and its pharmacological properties are being investigated for potential applications in drug discovery.
Used in Material Science:
2,4-Cyclohexadien-1-one, 6-(1,3-dihydro-1,3-dimethyl-2H-benzimidazol-2-ylidene)is also used in material science for the development of new materials with unique properties. Its chemical structure and functional groups can be utilized to create materials with specific characteristics, such as improved stability, enhanced reactivity, or novel optical, electronic, or mechanical properties. These materials can find applications in various industries, including electronics, coatings, and advanced materials.
Further research and development are necessary to fully explore the potential applications and benefits of 2,4-Cyclohexadien-1-one, 6-(1,3-dihydro-1,3-dimethyl-2H-benzimidazol-2-ylidene)in these industries and to optimize its synthesis and production methods for commercial use.
Check Digit Verification of cas no
The CAS Registry Mumber 113036-44-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,0,3 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 113036-44:
(8*1)+(7*1)+(6*3)+(5*0)+(4*3)+(3*6)+(2*4)+(1*4)=75
75 % 10 = 5
So 113036-44-5 is a valid CAS Registry Number.
113036-44-5Relevant academic research and scientific papers
Protocol for Visible-Light-Promoted Desulfonylation Reactions Utilizing Catalytic Benzimidazolium Aryloxide Betaines and Stoichiometric Hydride Donor Reagents
Hasegawa, Eietsu,Tanaka, Tsukasa,Izumiya, Norihiro,Kiuchi, Takehiro,Ooe, Yuuki,Iwamoto, Hajime,Takizawa, Shin-Ya,Murata, Shigeru
, p. 4344 - 4353 (2020/04/09)
An unprecedented photocatalytic system consisting of benzimidazolium aryloxide betaines (BI+-ArO-) and stoichiometric hydride reducing reagents was developed for carrying out desulfonylation reactions of N-sulfonyl-indoles,-amides, and-amines, and α-sulfonyl ketones. Measurements of absorption spectra and cyclic voltammograms as well as density functional theory (DFT) calculations were carried out to gain mechanistic information. In the catalytic system, visible-light-activated benzimidazoline aryloxides (BIH-ArO-), generated in situ by hydride reduction of the corresponding betaines BI+-ArO-, donate both an electron and a hydrogen atom to the substrates. A modified protocol was also developed so that a catalytic quantity of more easily prepared hydroxyaryl benzimidazolines (BIH-ArOH) is used along with a stoichiometric hydride donor to promote the photochemical desulfonylation reactions.
Formal Transfers of Hydride from Carbon-Hydrogen Bonds. Thermolysis of 2,3-dihydro-2-(2-hydroxyphenyl)-1,3-dimethyl-1H-benzimidazole
Montgrain, France,Ramos, Socorro M.,Wuest, James D.
, p. 1489 - 1492 (2007/10/02)
In 2,3-dihydro-2-(2-hydroxyphenyl)-1,3-dimethyl-1H-benzimidazole (3), the acidic hydrogen of a phenolic oxygen-hydrogen bond is near a carbon-hydrogen bond activated as a donor of hydride by two adjacent lone pairs in a dihydro aromatic ring.This juxtapos
