959624-24-9 Usage
Description
6-(hydroxyMethyl)-4-phenylchroMan-2-ol is a complex chemical compound that features a hydroxymethyl group, a phenyl group, and a chroman-2-ol moiety. This unique structure endows it with a range of properties that may be beneficial in various scientific and industrial applications, particularly in the fields of pharmaceutical and medicinal chemistry.
Uses
Used in Pharmaceutical Industry:
6-(hydroxyMethyl)-4-phenylchroMan-2-ol is used as a potential pharmaceutical agent due to its unique structure and possible biological activity. Its specific functional groups and molecular configuration may contribute to its efficacy in treating certain conditions or diseases.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 6-(hydroxyMethyl)-4-phenylchroMan-2-ol is utilized as a compound with potential therapeutic properties. Its intricate structure allows for exploration in drug design and development, possibly leading to new medications or therapies.
Used in Scientific Research:
6-(hydroxyMethyl)-4-phenylchroMan-2-ol serves as a subject of interest in scientific research, where its properties and potential uses are investigated. This can lead to a better understanding of its behavior in various chemical reactions and its interactions with biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 959624-24-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,9,6,2 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 959624-24:
(8*9)+(7*5)+(6*9)+(5*6)+(4*2)+(3*4)+(2*2)+(1*4)=219
219 % 10 = 9
So 959624-24-9 is a valid CAS Registry Number.
959624-24-9Relevant articles and documents
PROCESS FOR THE PREPARATION OF 2-HYDROXY-4-PHENYL-3,4-DIHYDRO-2H-CHROMEN-6-YL-METHANOL AND (R)-FESO-DEACYL
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Paragraph 0075, (2013/04/10)
The present invention regards an improved and industrially advantageous process for the preparation of the 2-hydroxy-4-phenyl-3,4-dihydro-2H-chromen-6-yl-methanol intermediates, also called “feso chromenyl” and (R)-2-[3-(diisopropylamino)-1-phenylpropyl]-4-(hydroxymethyl)phenol, also called “(R)-feso deacyl”, which are in turn used in the synthesis of fesoterodine and in particular of fesoterodine fumarate. This process utilises reagents which are non-toxic and manageable at industrial level and enables obtaining a new stable and non-hygroscopic crystalline form of the key intermediate “(R)-feso deacyl”, called form B.
PROCESS FOR THE PREPARATION OF 2 -HYDROXY- 4 -PHENYL -3, 4 -DIHYDRO-2H-CHROMEN- 6 -YL -METHANOL AND (R) - FESO - DEACYL
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Page/Page column 18-19, (2012/01/05)
The present invention regards an improved and industrially advantageous process for the preparation of the 2-hyaroxy-4-phenyl-3,4-dihydro-2H-chromen-6-yl-methanol intermediates, also called "feso chromenyl" and (R)-2-[3-(diisopropylamino)-l- phenylpropyl]-4-(hydroxymethyl)phenol, also called "(R)-feso deacyl", which are in turn used in the synthesis of fesoterodine and in particular of fesoterodine furnarate. This process utilises reagents which are non-toxic and manageable at industrial level and enables obtaining a new stable and non-hygroscopic crystalline form of the key intermediate "(R)-feso deacyl", called form B.
