791115-50-9 Usage
Explanation
The compound's full name, which includes its structure and functional groups.
Explanation
The compound belongs to the ester class of organic compounds, which are derived from acids and alcohols.
Explanation
The compound is widely used in various industrial and research applications, primarily as a solvent and an intermediate in the synthesis of other chemicals.
Explanation
The compound is known for its stability, making it a popular choice for various applications.
Explanation
The compound has low reactivity, which contributes to its stability and makes it suitable for use in different settings.
Explanation
The compound is used in the production of pharmaceuticals and can also be found in some consumer products.
Explanation
While the compound has many useful properties, it is essential to handle it with care due to potential health and safety risks.
Explanation
Proper handling and safety measures should be taken when working with this compound to minimize any risks associated with its use.
Category
Esters
Common Uses
Industrial and research settings, solvent, intermediate in chemical production
Stability
High
Reactivity
Low
Applications
Pharmaceutical manufacturing, consumer products
Health and Safety Risks
Potential hazards if not handled properly
Handling Precautions
Careful handling required
Check Digit Verification of cas no
The CAS Registry Mumber 791115-50-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,1,1,1 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 791115-50:
(8*7)+(7*9)+(6*1)+(5*1)+(4*1)+(3*5)+(2*5)+(1*0)=159
159 % 10 = 9
So 791115-50-9 is a valid CAS Registry Number.
791115-50-9Relevant articles and documents
2 - ((4R, 6R) - 6-aminomethyl-ethyl -2,2-dimethyl -1,3-dioxane-4-yl) acetate simple method for preparing
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Paragraph 0054-0055; 0062-0063, (2017/02/28)
The invention relates to a simple preparation method of 2-((4R,6R)-6-aminoethyl-2,2-dimethyl-1,3-dioxyhexacyclo-4-yl)acetate (I). The method comprises the following steps: reacting 3-cyanopropylene (II) and 3,3-dialkoxypropionate (III) or 3-alkoxyacrylate (IV) under the catalytic action of Lewis acid to prepare 2-((4R,6R)-6-cyanomethyl-2-ester-methyl-1,3-dioxyhexacyclo-4-yl)acetate (V), removing the solvent, directly carrying out blocking group conversion to prepare 2-((4R,6R)-6-cyanomethyl-2,2-dimethyl-1,3-dioxyhexacyclo-4-yl)acetate (VI), and carrying out Raney nickel catalytic hydrogenation two-step reaction to prepare (I). The stable form of the hexatomic ring chair-structure equatorial bond is utilized to construct the chiral center without using any additional chiral assistant. The method has the advantages of accessible raw materials, short reaction procedure and low cost, avoids carbonyl asymmetric reduction, is simple and environment-friendly, and is industrial production.
Asymmetric synthesis of the HMG-CoA reductase inhibitor atorvastatin calcium: An organocatalytic anhydride desymmetrization and cyanide-free side chain elongation approach
Chen, Xiaofei,Xiong, Fangjun,Chen, Wenxue,He, Qiuqin,Chen, Fener
, p. 2723 - 2728 (2014/04/17)
An efficient asymmetric synthesis of atorvastatin calcium has been achieved from commercially available diethyl 3-hydroxyglutarate through a novel approach that involves an organocatalytic enantioselective cyclic anhydride desymmetrization to establish C(
