34239-39-9 Usage
Carboxylic acid derivative
It is a compound derived from carboxylic acids, which are known for their acidic properties and functional groups (-COOH).
Class
2-hydroxy carboxylic acids This classification is based on the presence of a hydroxyl (-OH) group and a carboxylic acid (-COOH) group in the molecule.
Pharmaceutical industry use
Building block for drug synthesis 2-(1-hydroxycyclohexyl)propanoic acid serves as a key intermediate in the production of various drugs and pharmaceutical intermediates.
Manufacturing applications
Fragrances, flavors, and specialty chemicals The compound is used in the production of fragrances, flavors, and other specialty chemicals due to its unique properties.
Cosmetic industry potential
Moisturizing and antioxidant properties 2-(1-hydroxycyclohexyl)propanoic acid has potential applications in the cosmetic industry because of its ability to retain moisture and neutralize harmful free radicals.
Diverse industrial applications
The compound is an important intermediate in the production of a wide range of products, making it a versatile and valuable chemical in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 34239-39-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,2,3 and 9 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 34239-39:
(7*3)+(6*4)+(5*2)+(4*3)+(3*9)+(2*3)+(1*9)=109
109 % 10 = 9
So 34239-39-9 is a valid CAS Registry Number.
34239-39-9Relevant articles and documents
Irreversible aldolization of ketones with bisdicyclohexylboron enediolates
Ramachandran, P. Veeraraghavan,Otoo, Barnabas
supporting information, (2019/09/19)
Unlike the reported reversible addition of ketone enolborinates to ketones, the aldolization of ketones with bisboron enediolates derived from carboxylic acids proceeds without difficulty. A variety of α,β,β-trisubstituted-β-hydroxy acids have been thus s
AN EFFICIENT, HIGHLY REGIOSELECTIVE SYNTHESIS OF SUBSTITUTED (1-CYCLOHEXENYL) ACETIC ACID DERIVATIVES VIA IONIZATION/ELIMINATION OF β-LACTONES
Black, T. Howard,Maluleka, Stephen L.
, p. 531 - 534 (2007/10/02)
When treated with magnesium bromide, spiro β-lactones undergo an ionization/elimination reaction to afford cyclohexenyl acetic acid derivatives in high yield and isomeric purity.
Reaction de Reformatsky a froid avec des α-bromoesters-acetals. I. Une methode generale pour la synthese des β-hydroxyacides a partir des α-bromoesters de tetrahydropyrannyle (Note de laboratoire)
Bogavac, M.,Arsenijevic, L.,Arsenijevic, V.
, p. 145 - 147 (2007/10/02)
The readily accessible tetrahydropyranyl esters of α-bromoacids can be used in the Reformatsky reaction for the preparation of β-hydroxyacids.The reaction is generally carried out in cold tetrahydrofuran.The β-hydroxyacids can be easily obtained by stirring the cold solution of their tetrahydropyranyl esters with dilute hydrochloric acid.
