85820-84-4 Usage
Uses
Used in Organic Synthesis:
(2S)-3-azidopropane-1,2-diol is used as a precursor in the synthesis of other compounds for its unique reactivity and functional group.
Used in Pharmaceutical Applications:
(2S)-3-azidopropane-1,2-diol may have potential applications in medicine, depending on further studies and experiments to characterize its behavior and reactivity.
Used in Materials Science:
(2S)-3-azidopropane-1,2-diol may also have potential applications in materials science, given its unique chemical structure and properties.
Used in Industrial Applications:
(2S)-3-azidopropane-1,2-diol may be utilized in various industrial applications, leveraging its properties and reactivity for specific processes or products.
Check Digit Verification of cas no
The CAS Registry Mumber 85820-84-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,8,2 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 85820-84:
(7*8)+(6*5)+(5*8)+(4*2)+(3*0)+(2*8)+(1*4)=154
154 % 10 = 4
So 85820-84-4 is a valid CAS Registry Number.
85820-84-4Relevant academic research and scientific papers
Ring-opening of glycidyl derivatives by silanes mediated by Ti(O-i-Pr)4 or Al(O-i-Pr)3: Access to versatile C3 building blocks
Sutowardoyo,Sinou
, p. 437 - 444 (2007/12/18)
Ring-opening of chiral glycidol or glycidyl tosylate by Me3SiN3 or Me3SiCN catalyzed by Ti(O-i-Pr)4 or Al(O-i-Pr)3 occurred in a regiospecific manner and with very high stereoselectivity, leading to new trifunctionalized chiral building blocks. The enantiomeric excess of the ring-opened products was 90-95%, as determined by 1H NMR of the Mosher ester derivatives, indicating that there was no significant loss of optical purity during the ring-opening. This methodology was applied for the one-pot synthesis of (R)-1-azido-3-naphthyloxy-2-hydroxypropane in 94% ee, a precursor of analogs of propranolol.
