710-37-2 Usage
Description
(2E)-3-[(4-methylphenyl)sulfanyl]prop-2-enoic acid is a chemical compound with the molecular formula C10H10O2S. It is also known as 4-Methylphenyl 2-Propenoic acid and is a derivative of acrylic acid. (2E)-3-[(4-methylphenyl)sulfanyl]prop-2-enoic acid contains a thiol group (sulfanyl) and a double bond in its molecular structure, which contributes to its unique chemical properties and reactivity.
Uses
Used in Pharmaceutical Synthesis:
(2E)-3-[(4-methylphenyl)sulfanyl]prop-2-enoic acid is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Organic Compounds Synthesis:
This chemical compound is also used in the synthesis of organic compounds, where its thiol group and double bond can be utilized for various chemical reactions and the formation of new molecules.
Used in Organic Synthesis:
(2E)-3-[(4-methylphenyl)sulfanyl]prop-2-enoic acid is employed as a building block in organic synthesis, enabling the creation of complex organic molecules with diverse applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, this compound is used for the development of new therapeutic agents. Its unique structure and reactivity make it a valuable tool for designing and synthesizing novel pharmaceuticals with potential health benefits.
Overall, (2E)-3-[(4-methylphenyl)sulfanyl]prop-2-enoic acid has important synthetic and pharmaceutical uses, making it a valuable compound in the fields of chemistry and medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 710-37-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 0 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 710-37:
(5*7)+(4*1)+(3*0)+(2*3)+(1*7)=52
52 % 10 = 2
So 710-37-2 is a valid CAS Registry Number.
710-37-2Relevant articles and documents
Palladium-Catalyzed Synthesis of (Z)-3-Arylthioacrylic Acids and Thiochromenones
Palani, Thiruvengadam,Park, Kyungho,Song, Kwang Ho,Lee, Sunwoo
, p. 1160 - 1168 (2013/05/21)
The three-component reaction of aryl halides, sodium sulfide pentahydrate (Na2S×5 H2O), and propiolic acid in the presence of 2.5% bis(triphenylphosphine)palladium chloride [Pd(PPh3) 2Cl2], 5% 1,4-bis(diphenylphosphino)butane (dppb) and 2equivalents of 1,8-diazabicycloundec-7-ene (DBU) produces stereoselectively (Z)-3-arylthioacrylic acids in good yields. A study of the reaction pathway suggested that the C-S bond formation between aryl halides and Na 2S×5 H2O proceeded first, and the resulting intermediate reacted with propiolic acid to produce the desired product. In addition, when the resulting product was treated with acid, the respective thiochromenones were formed in good yields. Copyright
