10054-20-3 Usage
General Description
1-octadecyl-5-oxopyrrolidine-3-carboxylic acid, also known as OPC, is a synthetic compound that belongs to the family of fatty acid derivatives. It is often used in the manufacturing of skincare and cosmetic products due to its emollient and skin conditioning properties. OPC is also commonly used as a surfactant and emulsifying agent in various personal care and household products. In addition to its role in the cosmetic industry, OPC has also been studied for its potential biological activities, including antioxidant and anti-inflammatory properties, which may have implications for its use in pharmaceutical and medicinal applications. Overall, OPC is a versatile ingredient with various potential uses in the personal care and pharmaceutical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 10054-20-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,5 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10054-20:
(7*1)+(6*0)+(5*0)+(4*5)+(3*4)+(2*2)+(1*0)=43
43 % 10 = 3
So 10054-20-3 is a valid CAS Registry Number.
InChI:InChI=1/C23H43NO3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-24-20-21(23(26)27)19-22(24)25/h21H,2-20H2,1H3,(H,26,27)
10054-20-3Relevant articles and documents
Multicomponent Cascade Synthesis of Biaryl-Based Chalcones in Pure Water and in an Aqueous Micellar Environment
Armenise, Nicola,Malferrari, Danilo,Ricciardulli, Sara,Galletti, Paola,Tagliavini, Emilio
supporting information, p. 3177 - 3185 (2016/07/19)
The challenging multicomponent cascade synthesis of biaryl-based chalcones was carried out in pure water and in an aqueous micellar system. The first step of the protocol was a simple Pd-catalysed, ligand-free, and aerobic Suzuki–Miyaura reaction in aqueous medium. This proved to be extremely efficient for the coupling of aryl and heteroaryl bromides with different arylboronic acids. Subsequently, the resulting intermediates underwent an in-situ aldol condensation reaction to give biaryl(hetero)chalcones in good to excellent yields. When the protocol was applied to highly lipophilic or less reactive reagents, micellar catalysis was required for good results. To achieve this, we successfully used a new surfactant obtained from renewable resources that we recently designed. Furthermore, using this additive, the catalytic system can be repeatedly recycled without significant loss of activity.
