863705-27-5 Usage
Uses
Used in Pharmaceutical Research and Development:
2,5-Cyclohexadiene-1,4-dione, 2,5-dimethyl-3-(phenoxymethyl)is utilized as a key intermediate in the synthesis of novel pharmaceuticals, leveraging its reactivity and molecular structure to create new therapeutic agents. Its unique properties contribute to the exploration of its potential as a precursor in medicinal chemistry for developing innovative treatments.
Used in Organic Chemistry Reactions and Mechanisms:
2,5-Cyclohexadiene-1,4-dione, 2,5-dimethyl-3-(phenoxymethyl)serves as a valuable tool in organic chemistry for understanding reaction pathways and mechanisms. Its distinct structure allows chemists to probe the behavior of similar compounds under various conditions, thereby enhancing the knowledge base of organic reactions and contributing to the advancement of synthetic methodologies.
Used in the Synthesis of Organic Compounds:
2,5-Cyclohexadiene-1,4-dione, 2,5-dimethyl-3-(phenoxymethyl)is employed as a building block in the synthesis of a range of organic compounds. Its versatility in forming different chemical entities makes it an essential component in the creation of complex organic molecules with specific applications in various industries.
Used in Chemical Production:
In the chemical industry, 2,5-Cyclohexadiene-1,4-dione, 2,5-dimethyl-3-(phenoxymethyl)is used as a starting material or a catalyst in the production of various chemical products. Its role in these processes is crucial for the synthesis of specialty chemicals and materials with specific properties tailored for particular applications.
Check Digit Verification of cas no
The CAS Registry Mumber 863705-27-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,3,7,0 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 863705-27:
(8*8)+(7*6)+(6*3)+(5*7)+(4*0)+(3*5)+(2*2)+(1*7)=185
185 % 10 = 5
So 863705-27-5 is a valid CAS Registry Number.
863705-27-5Relevant academic research and scientific papers
Photoactivation of amino-substituted 1,4-benzoquinones for release of carboxylate and phenolate leaving groups using visible light
Chen, Yugang,Steinmetz, Mark G.
, p. 6053 - 6060 (2007/10/03)
Upon exposure to visible light, 2-pyrrolidino-substituted 3,6-dimethyl-1,4-benzoquinones photocyclize to give benzoxazolines with quantum yields of 0.07-0.10 in CH2Cl2, 0.02-0.04 in CH 3CN, and 3/su
Photochemical cyclization with release of carboxylic acids and phenol from pyrrolidino-substituted 1,4-benzoquinones using visible light
Chen, Yugang,Steinmetz, Mark G.
, p. 3729 - 3732 (2007/10/03)
(Chemical Equation Presented) Visible light irradiation of 5-acyloxymethyl- and 5-phenoxymethyl-2-pyrrolidino-1,4-benzoquinones effects photoisomerization to labile oxazolidines, which undergo elimination of carboxylate or phenolate leaving groups in high
