173300-94-2 Usage
Chemical Class
Phenols
Explanation
1,3-Benzenediol,2-(1-naphthalenyl)-(9CI) belongs to the class of phenols, which are aromatic compounds containing one or more hydroxyl groups attached to a benzene ring.
Explanation
This is an alternative name for the compound, which highlights the presence of two hydroxyl groups (dihydroxy) attached to a naphthalene molecule.
Explanation
The compound consists of a benzene ring with two hydroxyl groups (-OH) attached to it, along with a naphthalene group, which is a larger aromatic ring system.
Explanation
1,3-Benzenediol,2-(1-naphthalenyl)-(9CI) has been used as a starting material in the synthesis of different organic compounds due to its reactive functional groups.
Explanation
The compound has been studied for its potential applications in the biological and pharmaceutical fields, particularly for its antioxidant and antimicrobial properties, which can be beneficial in various therapeutic applications.
Explanation
1,3-Benzenediol,2-(1-naphthalenyl)-(9CI) is of interest to organic chemists due to its ability to participate in various chemical reactions and its potential for use in a wide range of synthetic pathways, making it a valuable compound for research and development.
Molecular Structure
Benzene ring with two hydroxyl groups and a naphthalene group
Precursor in Synthesis
Various organic compounds
Biological and Pharmaceutical Applications
Antioxidant and antimicrobial properties
Interest in Organic Chemistry
Versatile reactivity and potential for diverse synthetic routes
Check Digit Verification of cas no
The CAS Registry Mumber 173300-94-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,3,0 and 0 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 173300-94:
(8*1)+(7*7)+(6*3)+(5*3)+(4*0)+(3*0)+(2*9)+(1*4)=112
112 % 10 = 2
So 173300-94-2 is a valid CAS Registry Number.
173300-94-2Relevant articles and documents
Isothiourea-Catalyzed Atropselective Acylation of Biaryl Phenols via Sequential Desymmetrization/Kinetic Resolution
Brueckner, Alexander C.,Campbell, Andrew D.,Cheong, Paul Ha-Yeon,Feoktistova, Taisiia,Grove, Markas A.,Munday, Elizabeth S.,Slawin, Alexandra M. Z.,Smith, Andrew D.,Walden, Daniel M.,Young, Claire M.
, p. 7897 - 7905 (2020/03/23)
Axially chiral phenols are attractive targets in organic synthesis. This motif is central to many natural products and widely used as precursors to, or directly, as chiral ligands and catalysts. Despite their utility few simple catalytic methods are avail
Facile and highly enantioselective synthesis of axially chiral biaryls by enzymatic desymmetrization
Matsumoto,Konegawa,Nakamura,Suzuki
, p. 122 - 124 (2007/10/03)
The axially chiral biaryls 2 were obtained in high enantioselectivity by desymmetrization of the σ-symmetric biaryl diacetates 1 by lipase-catalyzed hydrolysis.
Enantioposition-selective alkynylation of biaryl ditriflates by palladium-catalyzed asymmetric cross-coupling
Kamikawa, Takashi,Uozumi, Yasuhiro,Hayashi, Tamio
, p. 3161 - 3164 (2007/10/03)
Asymmetric cross-coupling of prochiral biaryl ditriflate, 1-[2,6-bis[[(trifluoromethyl)sulfonyl]oxy]phenyl]naphthalene (1) or 1,3-bis[[(trifluoromethyl)sulfonyl]oxy]-2-(biphenyl-2-yl)benzene (4) with triphenylsilylethynylmagnesium bromide in the presence of lithium bromide and 5 mol% of palladium catalyst, PdCl2[(S)-Alaphos], proceeded with high enantioposition selectivity to give high yields of the corresponding axially chiral monoalkynylated biaryls, 2a or 2d, of high enantiomeric purity (up to >99% ee).
