55582-20-2 Usage
Molecular Structure
The compound features an isoindoline ring and a thioether functional group.
Explanation
The presence of these structural elements contributes to its unique properties and potential applications.
Explanation
The modification of the propanoic acid structure endows the compound with distinct properties and potential applications in various fields.
Explanation
This functional group is responsible for the compound's unique structure and may contribute to its biological activities.
Explanation
The presence of this group can influence the compound's reactivity, stability, and potential biological activities.
Explanation
Its unique structure and properties make it a promising candidate for the development of new drugs and organic compounds.
Explanation
This makes the compound of interest for further research and development in medicinal chemistry and drug discovery.
Derivative of Propanoic Acid
It is a derivative of propanoic acid with added functional groups.
1,3-Dioxo-1,3-Dihydro-2H-Isoindol-2-Yl Group
The compound contains a 1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl group.
Methylthio Group
The compound also contains a methylthio group.
Potential Applications
The compound has potential applications in pharmaceuticals and organic synthesis.
Biological Activities
Compounds with similar structural elements have shown potential for biological activities.
Check Digit Verification of cas no
The CAS Registry Mumber 55582-20-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,5,8 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 55582-20:
(7*5)+(6*5)+(5*5)+(4*8)+(3*2)+(2*2)+(1*0)=132
132 % 10 = 2
So 55582-20-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H11NO4S/c1-18-6-9(12(16)17)13-10(14)7-4-2-3-5-8(7)11(13)15/h2-5,9H,6H2,1H3,(H,16,17)/p-1/t9-/m0/s1
55582-20-2Relevant articles and documents
Photochemistry of the Phthalimide System, 37. - Thiazacycloalkanols by Photocyclization of S-Substituted N-(Thioalkyl)phthalimides
Sato, Yasuhiko,Nakai, Hideo,Wada, Masao,Mizoguchi, Tomishige,Hatanaka, Yasumaru,et al.
, p. 1099 - 1118 (2007/10/02)
N-Substituted phthalimides (1,2) possessing a terminal thioether function in their side chain were irradiated with a high-pressure mercury lamp to give a variety of thiazacycloalkanol derivatives (3,7,9-13,16,17) with favored γ-, δ-, ε-, and ζ-hydrogen abstractions (Table 1), in moderate to fairly good yields.
