83354-79-4 Usage
Uses
Used in Pharmaceutical Industry:
(4-Methylphenyl)(4-(beta-D-xylopyranosyloxy)phenyl)methanone hydrate is used as a compound for potential pharmaceutical applications due to its unique structure and properties. Further research is required to explore its specific uses and characteristics in this field.
Used in Organic Synthesis:
In the field of organic synthesis, (4-Methylphenyl)(4-(beta-D-xylopyranosyloxy)phenyl)methanone hydrate is used as a building block for the creation of more complex molecules. Its unique structure may allow for the development of novel compounds with various applications.
Used in Biochemical Research:
(4-Methylphenyl)(4-(beta-D-xylopyranosyloxy)phenyl)methanone hydrate is used as a research compound for studying its interactions with biological systems. Its potential applications in biochemical research may include understanding its effects on cellular processes or as a tool for investigating specific biological pathways.
Check Digit Verification of cas no
The CAS Registry Mumber 83354-79-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,3,5 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 83354-79:
(7*8)+(6*3)+(5*3)+(4*5)+(3*4)+(2*7)+(1*9)=144
144 % 10 = 4
So 83354-79-4 is a valid CAS Registry Number.
InChI:InChI=1/C19H20O6/c1-11-2-4-12(5-3-11)16(21)13-6-8-14(9-7-13)25-19-18(23)17(22)15(20)10-24-19/h2-9,15,17-20,22-23H,10H2,1H3/t15-,17+,18-,19+/m1/s1
83354-79-4Relevant academic research and scientific papers
Glycosylated Derivatives of Benzophenone, Benzhydrol, and Benzhydril as Potential Venous Antithrombotic Agents
Bellamy, Francois,Horton, Derek,Millet, Jean,Picart, Francois,Samreth, Soth,Chazan, Jean Bernard
, p. 898 - 903 (2007/10/02)
A series of glycosylated derivatives of benzophenone, benzhydrol, and benzhydril has been synthesized and evaluated for potential activity as venous antithrombotic agents.Studies on structure-activity relationships revealed that compounds having an electr
