259539-06-5 Usage
Uses
Used in Pharmaceutical Industry:
L-chiro-inositol is utilized as a therapeutic agent for the treatment of polycystic ovary syndrome (PCOS) and metabolic syndrome, as it has been shown to improve insulin sensitivity and ovarian function. Its potential role in cancer research also makes it a valuable compound for the development of novel pharmaceuticals.
Used in Research Applications:
In the field of scientific research, L-chiro-inositol serves as a key compound for studying its effects on insulin sensitivity, ovarian function, and its potential role in cancer research. This helps in advancing the understanding of its mechanisms of action and identifying new therapeutic targets.
Used in Dietary Supplements:
L-chiro-inositol can be found in some dietary supplements, where it is used to support insulin sensitivity and overall metabolic health. Its presence in these supplements aims to provide nutritional support for individuals seeking to improve their metabolic and hormonal balance.
Used in Cosmetics Industry:
Although not explicitly mentioned in the provided materials, L-chiro-inositol's potential role in improving insulin sensitivity and overall health may also make it a candidate for use in cosmetics and skincare products, where it could be employed for its beneficial effects on skin health and appearance.
Check Digit Verification of cas no
The CAS Registry Mumber 259539-06-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,9,5,3 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 259539-06:
(8*2)+(7*5)+(6*9)+(5*5)+(4*3)+(3*9)+(2*0)+(1*6)=175
175 % 10 = 5
So 259539-06-5 is a valid CAS Registry Number.
259539-06-5Relevant articles and documents
Intramolecular addition of carbon radicals to aldehydes: synthesis of enantiopure tetrahydrofuran-3-ols
Tiecco, Marcello,Testaferri, Lorenzo,Marini, Francesca,Sternativo, Silvia,Santi, Claudio,Bagnoli, Luana,Temperini, Andrea
, p. 5482 - 5489 (2008/01/07)
A simple and efficient substrate-controlled asymmetric synthesis of enantiopure tetrahydrofuran-3-ols by a 5-exo-trig radical cyclization is described. This cyclization occurs when a δ-carbon radical adds intramolecularly to the carbonyl group of an aldeh
Enantiospecific total synthesis of L-2',3'-dideoxyisonucleosides via regioselective opening of optically active C2-symmetric 1,4-pentadiene bis- epoxide
Jung,Kretschik
, p. 2975 - 2981 (2007/10/03)
A new method for the synthesis of L-2',3'-dideoxyisonucleosides is described. The readily available, optically active C2-symmetric bis-epoxide (2S,4S)-1,2:4,5-diepoxypentane (5) was prepared by a short route from readily available starting mate
