67759-10-8 Usage
Uses
Used in Organic Synthesis:
1-(4-(benzyloxy)-2-chlorophenyl)-2-(tert-butylamino)ethanol is utilized as a reagent in the field of organic synthesis, contributing to the creation of various complex organic molecules. Its unique structure allows it to participate in multiple chemical reactions, making it a valuable component in this application.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1-(4-(benzyloxy)-2-chlorophenyl)-2-(tert-butylamino)ethanol serves as an intermediate in the development of new drugs. Its structural diversity and reactivity make it a promising candidate for the synthesis of bioactive molecules with potential therapeutic applications.
Used in Chemical Intermediates:
1-(4-(benzyloxy)-2-chlorophenyl)-2-(tert-butylaMino)ethanol is also employed as a chemical intermediate in the production of other chemicals, leveraging its reactive functional groups to facilitate the synthesis of a wide range of chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 67759-10-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,7,5 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 67759-10:
(7*6)+(6*7)+(5*7)+(4*5)+(3*9)+(2*1)+(1*0)=168
168 % 10 = 8
So 67759-10-8 is a valid CAS Registry Number.
67759-10-8Relevant academic research and scientific papers
Synthesis of the β2-Agonist Tulobuterol and Its Metabolite 4-Hydroxytulobuterol
Burdeinyi, M. L.,Glushkova, M. A.,Popkov, S. V.
, p. 390 - 394 (2020/04/27)
Abstract: Alternative methods have been developed for the synthesis of theβ2-agonist tulobuterol and its metabolite4-hydroxytulobuterol with a similar activity. The proposed procedures utilizeavailable reagents, and the key stage in the synthesis is the formation ofintermediate oxirane according to the Corey–Chaykovsky reaction, followed byopening of the oxirane ring by the action of excess tert-butylamine. In the synthesis of 4-hydroxytulobuterol, thehydroxy group was protected by benzylation, and the protecting group was removedin the final stage by hydrogenation over carbon-supported palladium.
