43018-26-4 Usage
Uses
Used in Organic Synthesis:
2,6-bis(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)hexanoic acid is used as a versatile building block in organic synthesis for the creation of more complex molecules. Its unique structure and reactivity allow for the development of a wide range of organic compounds.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 2,6-bis(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)hexanoic acid is utilized as a key component in the synthesis of pharmaceuticals. Its chemical properties enable the design and development of novel drug candidates with potential therapeutic applications.
Used in Pharmaceutical Industry:
2,6-bis(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)hexanoic acid is used as a building block for the synthesis of pharmaceuticals, contributing to the development of new drugs with improved efficacy and safety profiles.
Used in Agrochemical Industry:
This chemical compound is also employed in the agrochemical industry as a component in the synthesis of agrochemicals, such as pesticides and herbicides, to enhance crop protection and yield.
Check Digit Verification of cas no
The CAS Registry Mumber 43018-26-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,3,0,1 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 43018-26:
(7*4)+(6*3)+(5*0)+(4*1)+(3*8)+(2*2)+(1*6)=84
84 % 10 = 4
So 43018-26-4 is a valid CAS Registry Number.
43018-26-4Relevant articles and documents
Palladium-Catalyzed Site-Selective Fluorination of Unactivated C(sp3)-H Bonds
Miao, Jinmin,Yang, Ke,Kurek, Martin,Ge, Haibo
supporting information, p. 3738 - 3741 (2015/08/18)
The transition-metal-catalyzed direct C-H bond fluorination is an attractive synthetic tool toward the preparation of organofluorines. While many methods exist for the direct sp3 C-H functionalization, site-selective fluorination of unactivated sp3 carbons remains a challenge. Direct, highly site-selective and diastereoselective fluorination of aliphatic amides via a palladium-catalyzed bidentate ligand-directed C-H bond functionalization process on unactivated sp3 carbons is reported. With this approach, a wide variety of β-fluorinated amino acid derivatives and aliphatic amides, important motifs in medicinal and agricultural chemistry, were prepared with palladium acetate as the catalyst and Selectfluor as the fluorine source.
The synthesis of N-acyl-2-hydroxymethyl aziridines of biological interest
Medjahed,Tabet Zatla,Kajima Mulengi,Baba Ahmed,Merzouk
, p. 1211 - 1213 (2007/10/03)
A practical synthesis of the title compounds from protected amino acylazides is described. All the compounds might be considered as a novel class of dipeptide isostere precursors; they all induce lymphocyte proliferation and protein production as observed from preliminary biological tests.
