75492-29-4 Usage
Description
(S)-2-methyloxetane, also known as (S)-3-methyloxetane, is a chemical compound characterized by the molecular formula C5H10O. It is a saturated cyclic ether featuring a six-membered ring that includes one oxygen atom and a methyl group attached to the second carbon atom. This colorless liquid exhibits a faint aromatic odor and is widely recognized for its applications in various industries.
Uses
Used in Organic Synthesis:
(S)-2-methyloxetane is utilized as a solvent in organic synthesis, playing a crucial role in facilitating chemical reactions and improving the efficiency of the synthesis process. Its unique structure and properties make it a valuable component in this application.
Used in Pharmaceutical Manufacturing:
In the pharmaceutical industry, (S)-2-methyloxetane serves as a key component in the manufacturing of various drugs. Its versatility and compatibility with different chemical compounds contribute to its significance in this field.
Used as a Reagent in Chemical Reactions:
(S)-2-methyloxetane is also employed as a reagent in chemical reactions, where it aids in the transformation of reactants into desired products. Its ability to participate in a range of reactions enhances its utility in this application.
Used in the Development of New Materials:
(S)-2-methyloxetane holds potential in the development of new materials, thanks to its unique structural properties and compatibility with other compounds. Its involvement in this area can lead to the creation of innovative materials with diverse applications.
Used as a Building Block for Complex Organic Molecules:
Lastly, (S)-2-methyloxetane is recognized for its potential as a building block in the synthesis of complex organic molecules. Its structural characteristics and reactivity make it a valuable component in the construction of intricate molecular structures with specific functions and properties.
Check Digit Verification of cas no
The CAS Registry Mumber 75492-29-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,4,9 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75492-29:
(7*7)+(6*5)+(5*4)+(4*9)+(3*2)+(2*2)+(1*9)=154
154 % 10 = 4
So 75492-29-4 is a valid CAS Registry Number.
75492-29-4Relevant articles and documents
OXYGEN YLIDES-II. PHOTOCHEMICAL AND RHODIUM-CATALYZED REACTIONS OF DIAZOMETHANE WITH (S)-2-METHYLOXETANE
Kirmse, Wolfgang,Chiem, Pham Van
, p. 197 - 200 (2007/10/02)
Photolysis of diazomethane in (S)-2-methyloxetane gives 2- and 3-methyltetrahydrofuran (1:3.2), the latter being formed with 21 percent net retention of configuration.In contrast, rhodium acetate catalysis yields racemic 3-methyltetrahydrofuran exclusively.
Access to (S)-2-Methyloxetane and the Precursor (S)-1,3-Butanediol of Hight Enantiomeric Purity
Hintzer, Klaus,Koppenhoefer, Bernhard,Schurig, Volker
, p. 3850 - 3854 (2007/10/02)
(S)-2-Methyloxetane (1) and its precursor (S)-1,3-butanediol (2) were prepared in low to moderate chemical yield with less than 0.5percent racemization from (S)-ethyl lactate (4) and from (2S,3S)-allothreonine (14b).For the first time the enantiomeric purities of both the starting material and the product (1) were carefully determined by high-precision capillary gas chromatography on optically active resolving stationary phases.The validity of the quadrant rule, correlating the relative configuration of alkyloxiranes with the order of elution from manganese(II) bis (3) by complexation gas chromatography, is also confirmed for 2-methyloxetane (1).
