190522-94-2 Usage
Uses
Used in Pharmaceutical Industry:
Benzenemethanol, 3-methoxy-a-(2-nitrophenyl)-4-(phenylmethoxy)is used as a pharmaceutical intermediate for the synthesis of various drugs and medications. Its unique structure and functional groups make it a valuable component in the development of new pharmaceutical compounds.
Used in Research Applications:
Benzenemethanol, 3-methoxy-a-(2-nitrophenyl)-4-(phenylmethoxy)is used as a research chemical to study its properties and potential applications in various scientific fields. Researchers may investigate its pharmacological or biological properties to better understand its potential uses and effects.
Used in Industrial Applications:
Benzenemethanol, 3-methoxy-a-(2-nitrophenyl)-4-(phenylmethoxy)may also have specific uses in industrial applications, such as in the development of new materials or processes. Its unique structure and functional groups could contribute to the creation of innovative products or techniques in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 190522-94-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,0,5,2 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 190522-94:
(8*1)+(7*9)+(6*0)+(5*5)+(4*2)+(3*2)+(2*9)+(1*4)=132
132 % 10 = 2
So 190522-94-2 is a valid CAS Registry Number.
190522-94-2Relevant academic research and scientific papers
Synthesis of [18F]Ro41-0960, a potent catechol-O-methyltransferase inhibitor, for PET studies
Ding,Sugano,Koomen,Aggarwal
, p. 303 - 318 (2007/10/03)
Ro41-0960 (3,4-dihydroxy-5-nitro-2'-fluorobenzophenone is a potent, fluorine containing COMT inhibitor. In order to map catechol-O-methyltransferase (COMT) in vivo with PET, no-carrier-added [18F]Ro41-0960 was synthesized by the nucleophilic aromatic substitution of [18F]fluoride for 2'-nitro on 3,4-dimethoxy-5,2'-dinitrobenzophenone, followed by hydrolysis with HBr. During the course of this study it was found that [18F]fluoromethane ([18F]CH3F) was generated as the side product of nucleophilic aromatic substitution reaction. Various precursors with different hydroxyl protecting groups were then investigated for the effects on this side reaction.
