101221-90-3 Usage
Uses
Used in Organic Synthesis:
[2S,3S,(+)]-1-Bromo-2,3-pentanediol is used as a building block in organic synthesis for the preparation of various pharmaceuticals and other organic compounds. Its versatile nature allows it to be used in the production of a wide range of chemical products.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, [2S,3S,(+)]-1-Bromo-2,3-pentanediol is used as a starting material for the synthesis of potential drug candidates. Its stereochemistry is crucial for the development of chiral molecules with specific biological activities, making it an important compound in the search for new therapeutic agents.
Used in Pharmaceutical Industry:
[2S,3S,(+)]-1-Bromo-2,3-pentanediol is used as a key intermediate in the pharmaceutical industry for the development of new drugs. Its unique stereochemistry allows for the creation of chiral molecules with targeted biological effects, which can be crucial in the treatment of various diseases and conditions.
Used in Chemical Research:
[2S,3S,(+)]-1-Bromo-2,3-pentanediol is also used in chemical research as a model compound to study the effects of stereochemistry on the properties and reactivity of molecules. This knowledge can be applied to the design and synthesis of new compounds with specific applications in various industries, including pharmaceuticals, materials science, and environmental science.
Check Digit Verification of cas no
The CAS Registry Mumber 101221-90-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,2,2 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 101221-90:
(8*1)+(7*0)+(6*1)+(5*2)+(4*2)+(3*1)+(2*9)+(1*0)=53
53 % 10 = 3
So 101221-90-3 is a valid CAS Registry Number.
101221-90-3Relevant academic research and scientific papers
Syntheses of Pure Enantiomers of erythro-1,2,3-Pentanetriol and their 1-Bromo- and 1-Tosyloxy Derivatives
Yusufoglu, Ayse,Antons, Stefan,Scharf, Hans-Dieter
, p. 1119 - 1123 (2007/10/02)
(2R,3S)- und (2S,3R)-erythro-1,2,3-Pentantriol (2a und 2b) wurden ausgehend von 2-Desoxy-D-erythro-pentose und ihrem L-Enantiomeren synthetisiert.Beide Substanzen sind ausgehend von D-(+)-Glucose und L-(+)-Arabinose erhaeltlich.Derivatisierung mittels sel
