170856-84-5 Usage
Description
3,4-Dihydro-1H-2-benzopyran-1S-acetic acid, a derivative of 2-benzopyran, is a chemical compound with the molecular formula C11H12O3. It is a flavonoid found in various plants, fruits, and vegetables, known for its antioxidant and anti-inflammatory properties. 3,4-DIHYDRO-1H-2-BENZOPYRAN-1S-ACETIC ACID has been studied for its potential health benefits, such as preventing cancer and cardiovascular diseases, and may also have applications in pharmaceuticals and new material development.
Uses
Used in Pharmaceutical Industry:
3,4-Dihydro-1H-2-benzopyran-1S-acetic acid is used as a pharmaceutical compound for its potential health benefits. It is believed to have antioxidant and anti-inflammatory properties, which may contribute to the prevention of cancer and cardiovascular diseases.
Used in Nutraceutical Industry:
In the nutraceutical industry, 3,4-Dihydro-1H-2-benzopyran-1S-acetic acid is used as a dietary supplement or functional food ingredient due to its potential health-promoting properties. Its antioxidant and anti-inflammatory effects may support overall health and well-being.
Used in Cosmetic Industry:
3,4-Dihydro-1H-2-benzopyran-1S-acetic acid is used as an active ingredient in cosmetic products for its potential skin health benefits. Its antioxidant properties may help protect the skin from environmental damage, while its anti-inflammatory effects may soothe and calm irritated skin.
Used in Material Science:
In the field of material science, 3,4-Dihydro-1H-2-benzopyran-1S-acetic acid may have potential applications in the development of new materials. Its unique chemical structure and properties could be utilized to create innovative materials with specific characteristics for various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 170856-84-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,0,8,5 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 170856-84:
(8*1)+(7*7)+(6*0)+(5*8)+(4*5)+(3*6)+(2*8)+(1*4)=155
155 % 10 = 5
So 170856-84-5 is a valid CAS Registry Number.
170856-84-5Relevant articles and documents
Copper-catalyzed enantioselective additions to oxocarbenium ions: Alkynylation of isochroman acetals
Maity, Prantik,Srinivas, Harathi D.,Watson, Mary P.
supporting information; experimental part, p. 17142 - 17145 (2011/12/13)
We have developed an enantioselective, copper(I)-catalyzed addition of terminal alkynes to racemic isochroman acetals. This method is one of the first transition-metal-catalyzed approaches to enantioselective additions to prochiral oxocarbenium ions. In this reaction, TMSOTf is used to form the oxocarbenium ion in situ under conditions compatible with simultaneous formation of the chiral copper acetylide. By using a bis(oxazoline) ligand, good yields and enantioselectivities are observed for a variety of enantioenriched 1-alkynyl isochromans.
(S)-(-)-4-[4-[2-(isochroman-1-yl)ethyl]-piperazin-1- yl]benzenesulfonamide, a selective dopamine D4 antagonist
TenBrink,Bergh,Duncan,Harris,Huff,Lahti,Lawson,Lutzke,Martin,Rees,Schlachter,Sih,Smith
, p. 2435 - 2437 (2007/10/03)
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