73048-42-7 Usage
Uses
Used in Coordination Chemistry:
2-(quinolin-8-yl)ethanol is used as a ligand for forming coordination compounds, which are essential in various chemical and biological processes. Its ability to bind with metal ions contributes to the stability and reactivity of these compounds.
Used in Organic Synthesis:
In the field of organic synthesis, 2-(quinolin-8-yl)ethanol is used as a building block for the creation of complex organic molecules. Its unique structure allows for versatile synthetic pathways, leading to the development of new pharmaceuticals and other chemical products.
Used in Oil Refineries:
2-(quinolin-8-yl)ethanol is used as a corrosion inhibitor in oil refineries to prevent the degradation of metal surfaces in contact with corrosive substances. This application helps to extend the lifespan of refinery equipment and reduce maintenance costs.
Used in Chemical Production:
As an intermediate in the production of dyes, antioxidants, pharmaceuticals, and other chemicals, 2-(quinolin-8-yl)ethanol plays a crucial role in the synthesis of these compounds. Its presence in the manufacturing process contributes to the development of a wide range of products with various applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 73048-42-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,0,4 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 73048-42:
(7*7)+(6*3)+(5*0)+(4*4)+(3*8)+(2*4)+(1*2)=117
117 % 10 = 7
So 73048-42-7 is a valid CAS Registry Number.
73048-42-7Relevant articles and documents
Smiles-type free radical rearrangement of aromatic sulfonates and sulfonamides: Syntheses of arylethanols and arylethylamines
Tada, Masaru,Shijima, Hiroyasu,Nakamura, Masaharu
, p. 2499 - 2505 (2007/10/03)
Smiles-type free radical rearrangements of arenesulfonates and arenesulfonamides are exploited for synthetic purposes. 4-Substituted benzenesulfonates cause Smiles-type rearrangement only when substituted by an electron withdrawing group. Therefore, ipso-sttack by an alkyl radical on arenesulfonates takes place in an electrophilic manner. Arenesulfonamides rearrange only when the amide nitrogen is substituted by an alkoxycarbonyl group, due to the electron withdrawing nature of this group. Sulfonates and the N-ethoxycarbonylsulfonamide derivatives of naphthalene, quinoline, and thiophene cause more rearrangement and show synthetic utility. Aromatic amino acid analogues were synthesized by Smiles-type rearrangement with moderate yields. The radical Smiles-type rearrangement of sulfonate and sulfonamide derivatives can be a useful synthetic route when we understand the electronic character of these reactions.
