37975-16-9 Usage
Uses
Used in Food Industry:
Curcumin is utilized as a food additive and coloring agent for its bright yellow color, adding visual appeal to a variety of food products.
Used in Pharmaceutical Industry:
Curcumin is employed for its medicinal properties, particularly its anti-inflammatory, antioxidant, and anticancer effects. It is being researched for its potential to treat a range of health conditions by modulating various biological pathways and exhibiting synergistic effects with conventional drugs.
Used in Cosmetic Industry:
Due to its antioxidant properties, Curcumin is also used in cosmetic products to protect the skin from oxidative stress and promote overall skin health.
Used in Research:
Curcumin's unique chemical structure and biological activities make it a subject of interest for scientific research, where it is studied for its potential applications in medicine and other fields.
Check Digit Verification of cas no
The CAS Registry Mumber 37975-16-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,9,7 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 37975-16:
(7*3)+(6*7)+(5*9)+(4*7)+(3*5)+(2*1)+(1*6)=159
159 % 10 = 9
So 37975-16-9 is a valid CAS Registry Number.
37975-16-9Relevant academic research and scientific papers
Boron difluoride β-diketonates: II. Synthesis of boron difluoride naphthoyl- and anisoylbenzoylmethanates substituted in the benzene ring
Gukhman,Reutov
, p. 1608 - 1611 (2007/10/03)
Destructive acylation of copper(II) naphthoyl- and anisoylacetonates with substituted benzoyl chlorides yielded β-diketones containing two aromatic substituents. Their reaction with boron trifluoride etherate in the presence of tributyl borate gave the co
Synthesis and antimicrobial activity of 1-(4-chlorophenyl)-3-(4-methoxy/3,4-dimethoxyphenyl)propan-1,3-diones and their 2-analogs
Singh, Rajvir,Malik, Om Parkash
, p. 455 - 459 (2007/10/02)
The condensation of substituted acetophenones 1-5 with 4-methoxy- or 3,4-dimethoxy-benzaldehyde (6,7) in ethanolic NaOH gives the corresponding substituted 2-propen-1-ones (8-17) which on bromination yields substituted propan-1-ones (18-27).Refluxing of 1