4989-59-7 Usage
Uses
Used in Pharmaceutical Industry:
2,3-di-3-pyridylbutane-2,3-diol is utilized as a building block in the synthesis of new drugs, contributing to the development of innovative pharmaceuticals. Its unique structure allows for the creation of diverse drug candidates with potential therapeutic applications.
Used in Chemical Processes:
As a reagent, 2,3-di-3-pyridylbutane-2,3-diol is employed in various chemical processes to facilitate reactions and improve the synthesis of target compounds. Its presence can enhance the efficiency and selectivity of these processes.
Used in Health and Environmental Research:
2,3-di-3-pyridylbutane-2,3-diol is being studied for its potential health effects and toxicity. Research is focused on understanding its impact on human health and the environment, ensuring the safe and responsible use of 2,3-di-3-pyridylbutane-2,3-diol in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 4989-59-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,8 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4989-59:
(6*4)+(5*9)+(4*8)+(3*9)+(2*5)+(1*9)=147
147 % 10 = 7
So 4989-59-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H16N2O2/c1-13(17,11-5-3-7-15-9-11)14(2,18)12-6-4-8-16-10-12/h3-10,17-18H,1-2H3
4989-59-7Relevant academic research and scientific papers
Photoaddition reactions of acetylpyridines with silyl ketene acetals: SET vs [2 + 2]-cycloaddition pathways
Cho, Dae Won,Park, Hea Jung,Yoon, Ung Chan,Lee, Hyang-Yeol,Mariano, Patrick S.
, p. 10304 - 10313 (2013/01/15)
Photoaddition reactions of silyl ketene acetals with 2-, 3- and 4-acetylpyridine have been explored. The results show that the acetylpyridines react with an electron rich, dimethyl-substituted silyl ketene acetal via a pathway in which excited state singl
PINACOLIC COUPLING OF AROMATIC ALDEHYDES AND KETONES PROMOTED BY AQUEOUS TITANIUM TRICHLORIDE IN BASIC MEDIA.
Clerici, A.,Porta, O.
, p. 3517 - 3520 (2007/10/02)
Aromatic aldehydes and ketones, which are not effected by aqueous titanium trichloride in acidic media, undergo rapid one-electron reduction to pinacols in basic media under very simple experimental conditions.The increase in the reducing power of the redox system with increasing the pH is discussed, and the stereoselectivity observed is shown in terms of Ti(IV) bridging control.
