41536-44-1 Usage
Description
2-(4-Morpholino)phenol, also known as 4-Morpholinophenol, is an organic compound characterized by the molecular formula C10H13NO2. It is a white to light yellow solid that serves as a versatile chemical intermediate in the synthesis of various organic compounds, including pharmaceuticals and dyes. This phenolic derivative features a morpholine substituent, which endows it with unique properties and makes it suitable for a range of applications in organic synthesis.
Uses
Used in Pharmaceutical Industry:
2-(4-Morpholino)phenol is used as a chemical intermediate for the synthesis of pharmaceuticals, owing to its ability to be incorporated into the molecular structures of various drugs. Its presence in these compounds can contribute to their therapeutic effects and properties.
Used in Dye Industry:
In the dye industry, 2-(4-Morpholino)phenol is utilized as a chemical intermediate in the production of dyes. Its chemical structure allows for the creation of dyes with specific color characteristics and properties, making it a valuable component in the formulation of various dyes.
Used in Color Photography:
2-(4-Morpholino)phenol is used as a developer in the production of color photographic prints. Its chemical properties enable it to react with the photographic emulsion, facilitating the development process and contributing to the final image quality.
Used in Water Treatment:
As a corrosion inhibitor, 2-(4-Morpholino)phenol is employed in water treatment to prevent the corrosion of metal surfaces in contact with water. Its presence in water systems helps to reduce the rate of corrosion, thereby extending the lifespan of equipment and infrastructure.
Used in Research and Development:
2-(4-Morpholino)phenol's potential biological activity makes it a target for research in the pharmaceutical industry. Scientists are interested in exploring its properties and effects to develop new drugs and therapies that can benefit human health.
Check Digit Verification of cas no
The CAS Registry Mumber 41536-44-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,5,3 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 41536-44:
(7*4)+(6*1)+(5*5)+(4*3)+(3*6)+(2*4)+(1*4)=101
101 % 10 = 1
So 41536-44-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO2/c12-10-4-2-1-3-9(10)11-5-7-13-8-6-11/h1-4,12H,5-8H2
41536-44-1Relevant articles and documents
Cu(II)-Catalyzed Ortho-Selective Amination of Simple Phenols with O-Benzoylhydroxylamines
Shao, Nan-Qi,Yao, Zhi-Li,Wang, Dong-Hui
, p. 429 - 432 (2020)
A Cu(II)-catalyzed ortho-selective amination of simple phenols with O-benzoylhydroxylamines has been developed, which provides access to 2-aminophenols under mild conditions. Various functional groups on the phenol and electrophilic amine are compatible, and the protocol typically delivers the products in moderate to good yields. The mechanistic detail of this process are discussed.
PRMT5 INHIBITORS CONTAINING A DIHYDRO- OR TETRAHYDROISOQUINOLINE AND USES THEREOF
-
, (2014/07/08)
Described herein are compounds of Formula (A), pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof. Compounds of the present invention are useful for inhibiting PRMT5 activity. Methods of using the compounds for treating PRMT5- mediated disorders are also described.
Function-oriented synthesis of a didesmethyl triazacryptand analogue for fluorescent potassium ion sensing
Carpenter, Richard D.,Verkman, Alan S.
experimental part, p. 1242 - 1248 (2011/04/17)
Triazacryptand (TAC)-based fluorescent K+ sensors have broad biomedical utility, yet their advancement has been hindered because of their challenging synthesis. Herein, an efficient synthesis is reported that delivers a didesmethyl triazacrypta
