53055-04-2 Usage
Description
(2-Nitro-3-methoxy-phenyl)-methanol, also known as NM-methanol, is a chemical compound characterized by the presence of a nitro and methoxy functional group attached to a benzene ring. It is a versatile molecule used in various applications due to its unique molecular structure and properties, making it significant in the fields of medicinal chemistry and materials science.
Uses
Used in Organic Synthesis:
(2-Nitro-3-methoxy-phenyl)-methanol is used as a starting material in organic synthesis for the creation of various biologically active compounds. Its functional groups facilitate multiple chemical reactions, contributing to the synthesis of a wide range of organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (2-Nitro-3-methoxy-phenyl)-methanol is utilized as a precursor for the development of new drugs. Its anti-inflammatory and analgesic properties make it a promising candidate for the treatment of pain and inflammation-related conditions.
Used in Corrosion Inhibition:
(2-Nitro-3-methoxy-phenyl)-methanol has been studied for its potential as a corrosion inhibitor in metal-based systems. Its chemical structure allows it to form protective layers on metal surfaces, reducing the rate of corrosion and extending the lifespan of metal components in various industrial applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (2-Nitro-3-methoxy-phenyl)-methanol is employed for the design and synthesis of novel therapeutic agents. Its unique properties enable the development of drugs with improved efficacy and reduced side effects, addressing unmet medical needs.
Used in Materials Science:
(2-Nitro-3-methoxy-phenyl)-methanol also finds applications in materials science, where it is used to develop new materials with specific properties. Its molecular structure allows for the creation of materials with tailored characteristics, such as improved stability, reactivity, or selectivity, for use in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 53055-04-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,0,5 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 53055-04:
(7*5)+(6*3)+(5*0)+(4*5)+(3*5)+(2*0)+(1*4)=92
92 % 10 = 2
So 53055-04-2 is a valid CAS Registry Number.
53055-04-2Relevant articles and documents
TRICYCLIC HETEROARYL COMPOUNDS USEFUL AS IRAK4 INHIBITORS
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Page/Page column 34-35, (2021/02/12)
Disclosed are compounds of Formula (I) or a salt or prodrug thereof, wherein: X11 and X22 are independently C or N, provided that zero or one of X11 and X22 is N; Ring A represented by the structure is: or; and Q, R11, R22, R33, R44, R66, and p are define herein. Also disclosed are methods of using such compounds as modulators of IRAK4, and pharmaceutical compositions comprising such compounds. These compounds are useful in treating, preventing, or slowing inflammatory and autoimmune diseases, or in the treatment of cancer.
TYK2 INHIBITORS AND USES THEREOF
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Paragraph 00309, (2020/09/27)
Described herein are compounds that are useful in treating a TYK2-mediated disorder. In some embodiments, the TYK2-mediated disorder is an autoimmune disorder, an inflammatory disorder, a proliferative disorder, an endocrine disorder, a neurological disorder, or a disorder associated with transplantation.
CLASS OF NEAR INFRARED MOLECULAR PROBES FOR BIOLOGICAL APPLICATIONS
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Paragraph 0088, (2014/10/16)
Methods for preparing 2,5-Bis(benzoxazol-2′-yl)benzene-1,4-diol derivatives (Zinhbo derivatives) are provided. Zinhbo derivatives are used to detect zinc ions and have particular application in vivo and in vitro. Zinhbo derivatives upon excitation give a florescence response emission that can be used to determine the presence of zinc cation in solution. Zinhbo derivatives complexed with zinc cations upon excitation can produce a florescence response emission in the visible and near infrared range. Zinhbo derivatives complexed with zinc cations exhibit a large stoke shift between the excitation and emission wavelengths.
