6971-20-6 Usage
Description
(E)-1-(2-hydroxy-3,4,6-trimethoxy-phenyl)-3-phenyl-prop-2-en-1-one, commonly known as curcumin, is a naturally occurring polyphenolic compound derived from the turmeric plant. It is characterized by its bright yellow color and is widely recognized for its potential health benefits, including anti-inflammatory, antioxidant, and anticancer properties. Curcumin's low toxicity and diverse biological activities make it a promising compound for pharmaceutical and dietary supplement development, as well as a popular choice as a food coloring and flavoring agent in Asian cuisines.
Uses
Used in Pharmaceutical Applications:
Curcumin is used as a therapeutic agent for its anti-inflammatory, antioxidant, and anticancer properties. It has been extensively studied for its potential to modulate various signaling pathways involved in inflammation, oxidative stress, and cancer progression. Its low toxicity and wide range of biological activities make it an attractive candidate for the development of pharmaceuticals targeting these conditions.
Used in Dietary Supplements:
Curcumin is utilized as an ingredient in dietary supplements due to its potential health benefits, including its anti-inflammatory, antioxidant, and anticancer properties. Its natural origin and low toxicity make it a safe and appealing option for consumers seeking to improve their overall health and well-being.
Used in Food Industry:
In the food industry, curcumin is used as a natural coloring agent to impart a vibrant yellow hue to various food products. Its unique flavor profile also contributes to the enhancement of taste in certain Asian cuisines, making it a valuable addition to the culinary world.
Used in Cosmetics:
Curcumin's anti-inflammatory and antioxidant properties have led to its application in the cosmetics industry, where it is used in skincare products to promote healthy skin and reduce signs of aging, inflammation, and oxidative stress.
Used in Antioxidant Applications:
Curcumin's potent antioxidant activity makes it a valuable compound for use in antioxidant applications, where it can help protect cells from damage caused by reactive oxygen species and other free radicals. This property is particularly useful in the development of pharmaceuticals and dietary supplements aimed at promoting overall health and reducing the risk of various diseases associated with oxidative stress.
Check Digit Verification of cas no
The CAS Registry Mumber 6971-20-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,7 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6971-20:
(6*6)+(5*9)+(4*7)+(3*1)+(2*2)+(1*0)=116
116 % 10 = 6
So 6971-20-6 is a valid CAS Registry Number.
InChI:InChI=1/C18H18O5/c1-21-14-11-15(22-2)18(23-3)17(20)16(14)13(19)10-9-12-7-5-4-6-8-12/h4-11,20H,1-3H3/b10-9+
6971-20-6Relevant articles and documents
A facile 2: H -chromene dimerization through an ortho -quinone methide intermediate catalyzed by a sulfonyl derived MIL-101 MOF
Du, Xin,Li, Xiujuan,Tang, Houliang,Wang, Wenyu,Ramella, Daniele,Luan, Yi
, p. 12722 - 12728 (2018/08/04)
A MIL-101-SO3H MOF was synthesized using commercially available materials. The as-synthesized MIL-101-SO3H was characterized by SEM, XRD, FTIR, BET and TGA. An efficient and diastereoselective homo-dimerization of 2H-chromenes cataly
Iron-catalyzed rearrangements and cycloaddition reactions of 2h-chromenes
Huan Sun, Yi Luan,Schaus, Scott E.
supporting information; experimental part, p. 6480 - 6483 (2012/02/01)
Iron(III) salts catalyze the tandem rearrangement/hetero-Diels-Alder reaction of 2H-chromenes to yield tetrahydrochromeno heterocycles. The process can occur as a homodimerization and cycloaddition process using electron-rich dienophiles. Deuterium labeli
