3952-36-1 Usage
Description
2-(9H-fluoren-9-yl)ethanol, also known as fluorenylmethanol, is a chemical compound with the molecular formula C15H14O. It belongs to the class of organic compounds known as fluorenes and derivatives. This colorless to slightly yellow liquid exhibits a floral odor and is soluble in water and most organic solvents. Its unique chemical properties and reactivity make it a valuable building block in the synthesis of various pharmaceuticals and organic compounds.
Uses
Used in Pharmaceutical Synthesis:
2-(9H-fluoren-9-yl)ethanol is used as a building block for the synthesis of various pharmaceuticals due to its unique chemical properties and reactivity.
Used in Organic Chemistry:
It serves as an intermediate in organic chemistry, contributing to the development of new compounds and materials.
Used in Drug Delivery Systems:
2-(9H-fluoren-9-yl)ethanol is used as a component in drug delivery systems, potentially enhancing the efficacy and targeted delivery of pharmaceutical agents.
Used in Polymer Synthesis:
It is utilized in the synthesis of polymers, which have a wide range of applications in various industries.
Used in Fragrance and Flavor Production:
2-(9H-fluoren-9-yl)ethanol is used as a solvent and intermediate in the production of fragrances and flavors, capitalizing on its floral odor.
Used in Industrial Applications:
It has been investigated for its potential use in the development of new materials and compounds for various industrial applications, showcasing its versatility and potential for innovation.
Check Digit Verification of cas no
The CAS Registry Mumber 3952-36-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,5 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3952-36:
(6*3)+(5*9)+(4*5)+(3*2)+(2*3)+(1*6)=101
101 % 10 = 1
So 3952-36-1 is a valid CAS Registry Number.
3952-36-1Relevant articles and documents
Studies on the alkylation and chlorination of fluorenes: Preparation of 9-(2-hydroxyethyl)fluorene and 2,7-dichloro-9-(2-hydroxyethyl)fluorene
Perumattam,Shao,Confer
, p. 1181 - 1184 (1994)
Efficient large-scale syntheses of 9-(2-hydroxyethyl)fluorene (1) and its 2,7-dichloro derivative 2 are described. Major differences exist in the reactivity of fluorene and its 2,7-dichloro derivative toward 9-alkylation. These differences are attributed to the difference in acidity of the protons in the 9-position of these compounds. Also 2,7-dichlorination of fluorene and its derivatives was satisfactorily achieved by treatment with NCS and conc. HCl in acetonitrile under carefully controlled conditions. Specifically, a highly concentrated solution of substrates and elevated temperatures were required for facile 2,7-dichlorination.
COLCHICINE DERIVATIVES OR PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF, METHOD FOR PREPARING SAID DERIVATIVES, AND PHARMACEUTICAL COMPOSITION COMPRISING SAID DERIVATIVES
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Paragraph 0063; 0064; 0065; 0066, (2013/03/26)
The present invention relates to colchicine derivatives expressed in chemical formula 1, or to pharmaceutically acceptable salts thereof, to a method for preparing said derivatives, and to a pharmaceutical composition comprising said derivatives. The colchicine derivatives according to the present invention exhibit superior immunomodulatory effects as compared with conventional immunomodulators or colchicines, and therefore can be valuably used as an immunomodulator for modulating an acute or chronic immune response in organ transplantation.
Fluorenyl derivatives
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, (2008/06/13)
The compound having the formula: STR1 and a method of treating an inflammatory condition comprising administering to an animal in need of such treatment an effective amount of at least one compound represented by the formula.
