116366-10-0 Usage
Uses
Used in Organic Chemistry:
(10H-Phenoxazin-1-yl)-diphenyl-methanol is used as a synthetic intermediate for the development of new organic compounds. Its distinctive structure allows for the creation of novel molecules with potential applications in various industries.
Used in Materials Science:
In materials science, (10H-Phenoxazin-1-yl)-diphenyl-methanol is used as a component in the design and synthesis of advanced materials. Its photophysical properties can contribute to the development of materials with specific optical, electronic, or sensing capabilities.
Used in Pharmaceutical Research:
(10H-Phenoxazin-1-yl)-diphenyl-methanol is utilized as a potential pharmaceutical agent in drug discovery and development. Its unique chemical structure may lead to the creation of new drugs with therapeutic benefits.
Used in Scientific Research:
As a research tool, (10H-Phenoxazin-1-yl)-diphenyl-methanol is used to study photochemical reactions and photophysical processes. Its properties can provide insights into the behavior of similar compounds and contribute to the advancement of scientific knowledge in these areas.
It is crucial to handle (10H-Phenoxazin-1-yl)-diphenyl-methanol with care and adhere to safety guidelines for its proper storage and use to mitigate any potential hazards associated with (10H-Phenoxazin-1-yl)-diphenyl-methanol.
Check Digit Verification of cas no
The CAS Registry Mumber 116366-10-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,3,6 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 116366-10:
(8*1)+(7*1)+(6*6)+(5*3)+(4*6)+(3*6)+(2*1)+(1*0)=110
110 % 10 = 0
So 116366-10-0 is a valid CAS Registry Number.
116366-10-0Relevant academic research and scientific papers
DIRECTED SYNTHESIS OF 1-SUBSTITUTED PHENOXAZINES
Katritzky, Alan R.,Miguel, Luis M. Vazques de,Rewcastle, Gordon W.
, p. 3135 - 3140 (2007/10/02)
Phenoxazine protected as its N-lithiocarbamate undergoes lithiation exclusively at the C-1 carbon atom.Reaction of the lithiated species with a variety of electrophiles readily produces several new 1-substituted phenoxazines, as well as two known compound
