61393-94-0 Usage
Description
(2S)-2-benzyloxirane, also known by its IUPAC name (2S)-2-phenyloxirane, is a chemical compound belonging to the class of organic compounds known as benzyloxiranes. It features a cyclic structure with one oxygen atom and a specific three-dimensional arrangement of atoms indicated by the "2S" in its name, which refers to its stereochemistry. This volatile and flammable liquid is widely used as a reagent in organic synthesis reactions due to its structure and reactivity.
Uses
Used in Organic Synthesis:
(2S)-2-benzyloxirane is used as a reagent in organic synthesis for its ability to participate in various chemical reactions, contributing to the production of a range of pharmaceuticals, agrochemicals, and other industrial products.
Used in Pharmaceutical Production:
In the pharmaceutical industry, (2S)-2-benzyloxirane is utilized as a building block in the synthesis of complex organic molecules, playing a crucial role in the development of new drugs and medicinal compounds.
Used in Agrochemical Production:
Similarly, in agrochemical manufacturing, (2S)-2-benzyloxirane serves as a key intermediate in the synthesis of various agrochemicals, helping to create effective products for agricultural applications.
Used in Industrial Product Development:
Beyond pharmaceuticals and agrochemicals, (2S)-2-benzyloxirane is also employed in the development of other industrial products, capitalizing on its reactivity and structural properties to enhance the creation of diverse chemical compounds and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 61393-94-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,3,9 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 61393-94:
(7*6)+(6*1)+(5*3)+(4*9)+(3*3)+(2*9)+(1*4)=130
130 % 10 = 0
So 61393-94-0 is a valid CAS Registry Number.
61393-94-0Relevant articles and documents
Asymmetric epoxidation of unfunctionalized olefins via formation of crystalline cyclodextrin complexes
Sakuraba, Hidetake,Tanaka, Yoshio
, p. 226 - 229 (1998)
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Azidolysis of epoxides catalysed by the halohydrin dehalogenase from Arthrobacter sp. AD2 and a mutant with enhanced enantioselectivity: an (S)-selective HHDH
Mikleu?evi?, Ana,Primo?i?, Ines,Hrenar, Tomica,Salopek-Sondi, Branka,Tang, Lixia,Elenkov, Maja Majeri?
, p. 930 - 935 (2016/09/13)
Halohydrin dehalogenase from Arthrobacter sp. AD2 catalysed azidolysis of epoxides with high regioselectivity and low to moderate (S)-enantioselectivity (E?=?1–16). Mutation of the asparagine 178 to alanine (N178A) showed increased enantioselectivity towards styrene oxide derivatives and glycidyl ethers. Conversion of aromatic epoxides was catalysed by HheA-N178A with complete enantioselectivity, however the regioselectivity was reduced. As a result of the enzyme-catalysed reaction, enantiomerically pure (S)-β-azido alcohols and (R)-α-azido alcohols (ee???99%) were obtained.
NICOTINIC ACETYLCHOLINE RECEPTOR LIGANDS AND THE USES THEREOF
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, (2013/07/25)
The invention relates to pyridinyl nicotinic acetylcholine receptor ligands, compositions comprising an effective amount of a pyridinyl nicotinic acetylcholine receptor ligand and methods to treat or prevent a condition, such as depression and nicotine dependence, comprising administering to an animal in need thereof an effective amount of a pyridinyl nicotinic acetylcholine receptor ligand.