83355-72-0 Usage
Uses
Used in Pharmaceutical Applications:
(4-((6-Deoxy-alpha-L-mannopyranosyl)oxy)phenyl)(4-nitrophenyl)methanon e is used as a pharmaceutical compound for its potential therapeutic properties. The presence of the 6-deoxy-alpha-L-mannopyranosyl group and the 4-nitrophenyl group may contribute to its interaction with biological targets, making it a candidate for drug development.
Used in Materials Science:
In the field of materials science, (4-((6-Deoxy-alpha-L-mannopyranosyl)oxy)phenyl)(4-nitrophenyl)methanon e may be utilized as a component in the development of novel materials with specific properties. Its unique structure could potentially be exploited to create materials with tailored characteristics for various applications.
Used in Organic Synthesis:
(4-((6-Deoxy-alpha-L-mannopyranosyl)oxy)phenyl)(4-nitrophenyl)methanon e can be used as a synthetic building block in organic synthesis. Its complex structure may allow for the creation of new compounds with diverse applications, ranging from pharmaceuticals to specialty chemicals.
Used in Research and Development:
(4-((6-Deoxy-alpha-L-mannopyranosyl)oxy)phenyl)(4-nitrophenyl)methanon e is also used in research and development settings to study its chemical properties, reactivity, and potential interactions with other molecules. Understanding these aspects can lead to the discovery of new applications and uses for (4-((6-Deoxy-alpha-L-mannopyranosyl)oxy)phenyl)(4-nitrophenyl)methanon e in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 83355-72-0 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 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 83355-72:
(7*8)+(6*3)+(5*3)+(4*5)+(3*5)+(2*7)+(1*2)=140
140 % 10 = 0
So 83355-72-0 is a valid CAS Registry Number.
InChI:InChI=1/C19H19NO8/c1-10-15(21)17(23)18(24)19(27-10)28-14-8-4-12(5-9-14)16(22)11-2-6-13(7-3-11)20(25)26/h2-10,15,17-19,21,23-24H,1H3/t10-,15-,17+,18+,19-/m0/s1
83355-72-0Relevant 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
