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<(2S,4S)-2-tert-butyl-4-methyl-5-oxo-1,3-dioxolan-4-yl>acetic acid is a carboxylic acid derivative with the molecular formula C11H18O4, belonging to the class of organic compounds known as lactones. It is a derivative of acetic acid, featuring a dioxolane ring structure, and is commonly utilized in organic synthesis and chemical research as a building block for constructing more complex molecules. The presence of a tert-butyl and a methyl group on the dioxolane ring endows it with unique steric and electronic properties, rendering it advantageous for a variety of chemical reactions and processes. Furthermore, the stereocenters at the second and fourth positions contribute to its chirality, potentially making it a valuable tool in asymmetric synthesis and catalysis.

92572-49-1

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92572-49-1 Usage

Uses

Used in Organic Synthesis:
<(2S,4S)-2-tert-butyl-4-methyl-5-oxo-1,3-dioxolan-4-yl>acetic acid is used as a building block in organic synthesis for creating more complex molecules due to its unique dioxolane ring structure and functional groups.
Used in Chemical Research:
In the field of chemical research, <(2S,4S)-2-tert-butyl-4-methyl-5-oxo-1,3-dioxolan-4-yl>acetic acid serves as a valuable compound for studying various chemical reactions and processes, particularly because of its steric and electronic properties conferred by the tert-butyl and methyl groups.
Used in Asymmetric Synthesis:
The chirality of <(2S,4S)-2-tert-butyl-4-methyl-5-oxo-1,3-dioxolan-4-yl>acetic acid, stemming from its stereocenters at the second and fourth positions, makes it a potentially valuable tool in asymmetric synthesis, where the selective formation of one enantiomer over another is crucial.
Used in Catalysis:
The stereochemistry of <(2S,4S)-2-tert-butyl-4-methyl-5-oxo-1,3-dioxolan-4-yl>acetic acid can also be exploited in catalysis, where the selective activation and transformation of substrates are highly desirable.
Used in Pharmaceutical Industry:
<(2S,4S)-2-tert-butyl-4-methyl-5-oxo-1,3-dioxolan-4-yl>acetic acid is used as an intermediate in the pharmaceutical industry for the development of new drugs, taking advantage of its unique structural features and reactivity.
Used in Material Science:
In material science, <(2S,4S)-2-tert-butyl-4-methyl-5-oxo-1,3-dioxolan-4-yl>acetic acid may be employed as a component in the synthesis of novel materials with specific properties, such as polymers with tailored characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 92572-49-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,5,7 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 92572-49:
(7*9)+(6*2)+(5*5)+(4*7)+(3*2)+(2*4)+(1*9)=151
151 % 10 = 1
So 92572-49-1 is a valid CAS Registry Number.

92572-49-1Upstream product

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