61000-04-2 Usage
Uses
Used in Pharmaceutical Industry:
Curcumenone is used as a pharmaceutical agent for its anti-inflammatory, antioxidant, and anti-cancer properties. Its various biological activities make it a promising candidate for the development of new therapeutic agents.
Used in Drug Delivery Systems:
Curcumenone can be employed in drug delivery systems to improve the delivery, bioavailability, and therapeutic outcomes of various medications. Its unique chemical structure and biological activities can be utilized to enhance the efficacy of drug delivery systems.
Used in Nutraceutical Industry:
Curcumenone can be used as a nutraceutical ingredient due to its antioxidant and anti-inflammatory properties. It can be incorporated into dietary supplements and functional foods to provide health benefits and support overall well-being.
Used in Cosmetic Industry:
Curcumenone can be used in the cosmetic industry for its anti-inflammatory and antioxidant properties. It can be incorporated into skincare products to provide anti-aging, skin-soothing, and protective benefits.
Used in Food Industry:
Curcumenone can be used in the food industry as a natural preservative and flavoring agent. Its antioxidant properties can help extend the shelf life of food products, while its unique chemical structure can contribute to the flavor profile of various dishes.
Check Digit Verification of cas no
The CAS Registry Mumber 61000-04-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,0,0 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 61000-04:
(7*6)+(6*1)+(5*0)+(4*0)+(3*0)+(2*0)+(1*4)=52
52 % 10 = 2
So 61000-04-2 is a valid CAS Registry Number.
61000-04-2Relevant academic research and scientific papers
Chiral 1,3,2-Diazaphospholenes as Catalytic Molecular Hydrides for Enantioselective Conjugate Reductions
Miaskiewicz, Solène,Reed, John H.,Donets, Pavel A.,Oliveira, Caio C.,Cramer, Nicolai
supporting information, p. 4039 - 4042 (2018/03/13)
Secondary 1,3,2-diazaphospholenes have a polarized P?H bond and are emerging as molecular hydrides. Herein, a class of chiral, conformationally restricted methoxy-1,3,2-diazaphospholene catalysts is reported. We demonstrate their catalytic potential in asymmetric 1,4-reductions of α,β-unsaturated carbonyl derivatives, including enones, acyl pyrroles, and amides, which proceeded in enantioselectivities of up to 95.5:4.5 e.r.
A New Approach to the Stereoselective Synthesis of β-methylchalcones
Elmorsy, Saad S.,Khalil, Abdel Galel M.,Girges, M. M.,Salama, Tarek A.
, p. 1537 - 1544 (2007/10/03)
Many β-methylchalcone derivatives have been prepared from self condensation of aralkyl ketones mediated by tetrachlorosilane-ethanol in mild conditions. - Key words: aralkyl ketones; tetrachlorosilane; β-methylchalcones; triarylbenzene derivatives
