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Ethanone, 1-(2-chloro-5-hydroxyphenyl)is a chemical compound characterized by the presence of a ketone functional group attached to a phenyl ring, which is substituted with a chlorine atom and a hydroxyl group. This unique structure may endow the compound with distinct properties and potential biological activities, making it a candidate for various applications.

58020-38-5

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58020-38-5 Usage

Uses

Used in Pharmaceutical Applications:
Ethanone, 1-(2-chloro-5-hydroxyphenyl)is used as a potential pharmaceutical agent due to its unique chemical structure. The chlorine substituent may enhance the compound's stability and reactivity, while the hydroxyl group could contribute to its solubility and interactions with biological systems. This makes it a promising candidate for the development of new drugs and therapeutics.
Further research is needed to explore the potential uses and properties of Ethanone, 1-(2-chloro-5-hydroxyphenyl)in various fields, as its full potential has not yet been fully realized.

Check Digit Verification of cas no

The CAS Registry Mumber 58020-38-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,0,2 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 58020-38:
(7*5)+(6*8)+(5*0)+(4*2)+(3*0)+(2*3)+(1*8)=105
105 % 10 = 5
So 58020-38-5 is a valid CAS Registry Number.

58020-38-5Relevant academic research and scientific papers

8-AZABICYCLO[3.2.1]OCTANE-8-CARBOXAMIDE DERIVATIVE

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Page/Page column 53, (2012/09/11)

Disclosed is a compound represented by formula (1) or a pharmacologically acceptable salt thereof (In the formula, A represents a group that is represented by formula (A-1); R1a and R1b may be the same or different and each independently represents a C1-6 alkyl group which may be substituted by one to three halogen atoms; m and n each independently represents an integer of 0-5; X1 represents a hydroxyl group or an aminocarbonyl group; Z1 represents a single bond or the like; and R2 represents an optionally substituted C1-6 alkyl group, an optionally substituted C6-10 aryl group or the like.)

Facile p-toluenesulfonic acid-promoted para-selective monobromination and chlorination of phenol and analogues

Bovonsombat, Pakorn,Ali, Rameez,Khan, Chiraphorn,Leykajarakul, Juthamard,Pla-On, Kawin,Aphimanchindakul, Suraj,Pungcharoenpong, Natchapon,Timsuea, Nisit,Arunrat, Anchalee,Punpongjareorn, Napat

experimental part, p. 6928 - 6935 (2010/10/01)

para-Regioselective bromination of phenol and analogues, promoted by p-toluenesulfonic acid, is achieved in high to excellent yields at room temperature with N-bromosuccinimide. Chlorination with N-chlorosuccinimide and catalysed by p-toluenesulfonic acid also gives para-chlorinated phenol analogues in good yields at room temperature. para-Bromination of phenol, promoted by p-toluenesulfonic acid, is achieved in excellent yields at room temperature with N-bromosuccinimide. p-Toluenesulfonic acid is also effective as a promoter of para-chlorination with N-chlorosuccinimide.

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