16820-37-4 Usage
Uses
Used in Pharmaceutical Industry:
3,6-Dimethyl-benzofuran-2-carboxylic acid is used as a building block for the synthesis of various pharmaceuticals due to its antimicrobial, anti-inflammatory, anti-cancer, and anti-oxidant properties. Its diverse potential applications make it a promising candidate for the development of new drugs in the medical field.
Used in Agrochemical Industry:
3,6-Dimethyl-benzofuran-2-carboxylic acid is also used as a building block in the synthesis of agrochemicals. Its antimicrobial properties can be harnessed for the development of new pesticides or fungicides, contributing to the advancement of agriculture and crop protection.
Used in Antimicrobial Applications:
3,6-Dimethyl-benzofuran-2-carboxylic acid is used as an antimicrobial agent for its ability to inhibit the growth of various microorganisms. This property makes it a valuable ingredient in the development of new antimicrobial drugs and products.
Used in Anti-inflammatory Applications:
The anti-inflammatory properties of 3,6-Dimethyl-benzofuran-2-carboxylic acid make it suitable for use in the development of anti-inflammatory drugs. It can help alleviate inflammation and reduce the associated symptoms in various medical conditions.
Used in Anti-cancer Applications:
3,6-Dimethyl-benzofuran-2-carboxylic acid has been studied for its potential anti-cancer activities. It can be used as a component in the development of new cancer treatments, targeting and inhibiting the growth of cancer cells.
Used in Anti-oxidant Applications:
The anti-oxidant properties of 3,6-Dimethyl-benzofuran-2-carboxylic acid make it a valuable ingredient in the development of anti-oxidant products. It can help protect cells from oxidative damage and support overall health and well-being.
Check Digit Verification of cas no
The CAS Registry Mumber 16820-37-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,8,2 and 0 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 16820-37:
(7*1)+(6*6)+(5*8)+(4*2)+(3*0)+(2*3)+(1*7)=104
104 % 10 = 4
So 16820-37-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H10O3/c1-6-3-4-8-7(2)10(11(12)13)14-9(8)5-6/h3-5H,1-2H3,(H,12,13)
16820-37-4Relevant academic research and scientific papers
A convenient procedure for the synthesis of substituted 4-methylaminocoumarins
Al-Zghoul, Khadeejh H.,Salih, Kifah S.M.,Ayoub, Mikdad T.,Mubarak, Mohammad S.
, p. 2937 - 2947 (2007/10/03)
3-Bromo-7-methoxy-4-methylcoumarin and 3-bromo-4,7-dimethyl-coumarin give a mixture of the corresponding 3-aminocoumarins and 4-aminomethylcoumarins upon the reaction with a number of secondary amines. In addition, the reaction of 7-methoxy- and 7-methyl-4-bromomethylcoumarins with secondary diamines affords the corresponding, N,N-dicoumarinmethyldiamine.
Benzofuran Derivatives. Part 4. Synthesis of Benzofurans and 2,3,4,5-Tetrahydro-1-benzoxepin-3,5-diones
Suzuki, Tsuneo,Tanemura, Kiyoshi,Horaguchi, Takaaki,Shimimizu, Takahachi,Sakakibara, Tohru
, p. 423 - 429 (2007/10/02)
By treatment of ethyl 4- or 5-substituted 2-acetylphenoxyacetates 1 with potassium hydroxide in dry dioxane, benzofurans 2-7 and 2,3,4,5-tetrahydro-1-benzoxepin-3,5-diones 8 were obtained.The relative yields of benzofurans 2-7 and 2,3,4,5-tetrahydro-1-benzoxepin-3,5-diones 8 varied with the types of 4- or 5-substituents.The electron-donating 4-methoxyl group favored the formation of benzoxepins.On the other hand, electron-withdrawing substituents such as the 4-nitro group favored the formation of benzofurans.When esters 1 were treated with sodium amide,2,3-dihydrobenzofurans 2 were obtained exclusively regardless of 4- or 5-substituents.
