857653-94-2 Usage
General Description
The chemical [3-(4-pyridinyl)-1,2,4-oxadiazol-5-yl]methanol, also known as SALTDATA: FREE, is a compound with a pyridinyl group and an oxadiazolyl group attached to a methanol group. It is commonly used in pharmaceutical and research applications due to its potential biological activity and ability to modulate specific protein targets. The compound has been studied for its potential use in treating various diseases and disorders, and its structure makes it a promising candidate for further research and development. Additionally, it is important to handle and store this chemical with care, following standard safety protocols and practices.
Check Digit Verification of cas no
The CAS Registry Mumber 857653-94-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,7,6,5 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 857653-94:
(8*8)+(7*5)+(6*7)+(5*6)+(4*5)+(3*3)+(2*9)+(1*4)=222
222 % 10 = 2
So 857653-94-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H7N3O2/c12-5-7-10-8(11-13-7)6-1-3-9-4-2-6/h1-4,12H,5H2
857653-94-2Relevant articles and documents
One-step protection-free synthesis of 3-aryl-5-hydroxyalkyl-1,2,4- oxadiazoles as building blocks
Neves Filho, Ricardo A. W.,Da Silva-Alves, Diana C. B.,Dos Anjos, Janaina V.,Srivastava, Rajendra M.
supporting information, p. 2596 - 2602 (2013/07/26)
A simple and straightforward synthesis of 3-aryl-5-hydroxyalkyl-1,2,4- oxadiazoles is described. The reaction among arylamidoximes, ethyl glycolate or ethyl lactate, and potassium carbonate in refluxing toluene afforded the desired 1,2,4-oxadiazoles in moderate to good yields. The synthesis has been accomplished in a single step, avoiding protection-deprotection protocols. Supplemental materials are available for this article. Go to the publisher's online edition of Synthetic Communications to view the free supplemental file.
