155322-89-7 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
2. Derivative of 1,3-dioxolane
Explanation
It is a chemical compound derived from the parent compound 1,3-dioxolane, which is a heterocyclic compound containing two oxygen atoms.
3. Chiral compound
Explanation
A chiral compound is one that has a chiral center, meaning it has a specific stereochemistry that makes it non-superimposable on its mirror image.
4. (4S,5R)configuration
Explanation
This indicates the specific stereochemistry of the compound, with the S (sinister) and R (rectus) designations referring to the spatial arrangement of the atoms around the chiral centers.
5. Used in synthesis of pharmaceuticals and agrochemicals
Explanation
The compound serves as a building block or intermediate in the production of various pharmaceuticals and agrochemicals, which are chemicals used in the medical and agricultural industries, respectively.
6. Versatile building block in organic synthesis
Explanation
It is a valuable reagent in organic chemistry due to its ability to be used in a wide range of reactions to form different compounds.
7. Reactive and potentially hazardous substance
Explanation
The compound should be handled with care, as it can react with other substances and may pose health or environmental risks if not properly managed.
8. Commonly used as a reagent
Explanation
It is frequently employed in chemical reactions as a starting material or catalyst to facilitate the formation of desired products.
Check Digit Verification of cas no
The CAS Registry Mumber 155322-89-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,3,2 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 155322-89:
(8*1)+(7*5)+(6*5)+(5*3)+(4*2)+(3*2)+(2*8)+(1*9)=127
127 % 10 = 7
So 155322-89-7 is a valid CAS Registry Number.
155322-89-7Relevant academic research and scientific papers
Ziegler, Frederick E.,Kim, Hakwon
, p. 7669 - 7672 (1993)
A short, stereoselective synthesis of (-)-acetomycin (2) from L-threonine is reported.The final step in the synthesis is a selective Baeyer-Villiger oxidation that discriminates between two methyl ketones.
