104216-46-8 Usage
Description
3-[(3,4-DIMETHYLPHENYL)THIO]PROPANOIC ACID is a thioether derivative of propionic acid with the molecular formula C12H16O2S. It is a carboxylic acid characterized by a molecular weight of 224.32 g/mol and a unique structure that includes a thioether group and two methyl substituents on the phenyl ring. This chemical compound is commonly used as a food preservative and may have potential applications in various industries such as pharmaceuticals, agrochemicals, and materials science due to its distinctive chemical properties.
Uses
Used in Food Industry:
3-[(3,4-DIMETHYLPHENYL)THIO]PROPANOIC ACID is used as a food preservative for its ability to inhibit the growth of microorganisms, thereby extending the shelf life of food products.
Used in Pharmaceutical Industry:
3-[(3,4-DIMETHYLPHENYL)THIO]PROPANOIC ACID is used as an active pharmaceutical ingredient or as an intermediate in the synthesis of drugs, leveraging its unique chemical structure to target specific biological pathways or receptors.
Used in Agrochemical Industry:
3-[(3,4-DIMETHYLPHENYL)THIO]PROPANOIC ACID is used as a component in agrochemical products, such as pesticides or herbicides, to protect crops from pests and enhance agricultural productivity.
Used in Materials Science:
3-[(3,4-DIMETHYLPHENYL)THIO]PROPANOIC ACID is used in the development of new materials, such as polymers or coatings, due to its chemical properties that may impart specific characteristics like improved stability or reactivity.
However, it is important to note that additional research is necessary to fully understand the potential uses and effects of 3-[(3,4-DIMETHYLPHENYL)THIO]PROPANOIC ACID in these industries.
Check Digit Verification of cas no
The CAS Registry Mumber 104216-46-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,2,1 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 104216-46:
(8*1)+(7*0)+(6*4)+(5*2)+(4*1)+(3*6)+(2*4)+(1*6)=78
78 % 10 = 8
So 104216-46-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H14O2S/c1-8-3-4-10(7-9(8)2)14-6-5-11(12)13/h3-4,7H,5-6H2,1-2H3,(H,12,13)
104216-46-8Relevant articles and documents
Cu(I)-Catalyzed Enantioselective Alkynylation of Thiochromones
Chang, Xiaoyong,Lin, Zhenyang,Meng, Ling,Ngai, Ka Yan,Wang, Jun
supporting information, p. 1155 - 1159 (2020/02/26)
A highly efficient asymmetric synthesis of chiral thiochromanones is developed via Cu(I)/phosphoramidite catalyzed asymmetric alkynylation of thiochromones under mild reaction conditions. The catalyst system is tolerant of various thiochromone precursors and terminal alkynes. The established asymmetric transformation provides different enatiomeric-enriched thiochromanones with more molecular complexity and enables access to chiral thioflavanones, a subgroup of flavonoid by further functionalization.
Cu-Catalyzed Conjugate Addition of Grignard Reagents to Thiochromones: An Enantioselective Pathway for Accessing 2-Alkylthiochromanones
Luo, Shihui,Meng, Ling,Yang, Qingxiong,Wang, Jun
supporting information, p. 2071 - 2075 (2018/09/18)
The enantioselective incorporation of alkyl groups in thiochromones was realized for the first time by a Cu/(R, S)-PPF-P t Bu 2 -catalyzed conjugate addition of Grignard reagents to thiochromones. With this method, a series of 2-methylthiochromanones were obtained in good yields (up to 96% yield) with moderate-to-good ee values (up to 87% ee). The established method expedites the synthesis of a large library of chiral thiochromanones for further synthetic applications and biological studies.