69500-53-4 Usage
Description
(S)-4-[4-(Oxiranylmethoxy)-1,2,5-thiadiazol-3-yl]morpholine, with the CAS number 69500-53-4, is an organic compound that holds significant value in the field of organic synthesis. It is characterized by its unique chemical structure, which incorporates a morpholine ring and a 1,2,5-thiadiazol-3-yl group, making it a versatile building block for the development of various chemical compounds.
Uses
Used in Organic Synthesis:
(S)-4-[4-(Oxiranylmethoxy)-1,2,5-thiadiazol-3-yl]morpholine is used as a synthetic building block for the creation of a wide range of chemical compounds. Its unique structure allows for the formation of diverse molecules with potential applications in various industries, such as pharmaceuticals, agrochemicals, and materials science.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (S)-4-[4-(Oxiranylmethoxy)-1,2,5-thiadiazol-3-yl]morpholine is used as a key intermediate in the synthesis of novel drug candidates. Its incorporation into drug molecules can potentially enhance their pharmacological properties, such as potency, selectivity, and bioavailability, leading to the development of more effective therapeutic agents.
Used in Agrochemical Industry:
(S)-4-[4-(Oxiranylmethoxy)-1,2,5-thiadiazol-3-yl]morpholine is also utilized in the agrochemical industry for the synthesis of new pesticides and other crop protection agents. Its unique chemical structure can be exploited to design molecules with improved activity against pests and diseases, as well as reduced environmental impact.
Used in Materials Science:
In the field of materials science, (S)-4-[4-(Oxiranylmethoxy)-1,2,5-thiadiazol-3-yl]morpholine can be employed as a component in the development of advanced materials with specific properties. These materials may find applications in areas such as electronics, coatings, and adhesives, where their unique characteristics can provide advantages over existing materials.
Check Digit Verification of cas no
The CAS Registry Mumber 69500-53-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,5,0 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 69500-53:
(7*6)+(6*9)+(5*5)+(4*0)+(3*0)+(2*5)+(1*3)=134
134 % 10 = 4
So 69500-53-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H13N3O3S/c1-3-13-4-2-12(1)8-9(11-16-10-8)15-6-7-5-14-7/h7H,1-6H2/t7-/m0/s1
69500-53-4Relevant articles and documents
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McClure,D.E. et al.
, p. 1826 - 1831 (1979)
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Enantioselective synthesis of (S)-timolol via kinetic resolution of terminal epoxides and dihydroxylation of allylamines
Narina, Srinivasarao V.,Sudalai, Arumugam
, p. 3026 - 3030 (2007/10/03)
An efficient enantioselective synthesis of (S)-timolol has been described using chiral Co-salen-catalyzed kinetic resolution of less expensive (±)-epichlorohydrin with 3-hydroxy-4-(N-morpholino)-1,2,5-thiadiazole in good overall yield (55%) and excellent enantioselectivity (98%). Synthesis of (S)-timolol has also been achieved using hydrolytic kinetic resolution as well as asymmetric dihydroxylation routes in 90% ee and 56% ee, respectively.
Arenesulfonate Derivatives of Homochiral Glycidol: Versatile Chiral Building Blocks for Organic Synthesis
Klunder, Janice M.,Onami, Tetsuo,Sharpless, K. Barry
, p. 1295 - 1304 (2007/10/02)
The preparation of a series of crystalline arenesulfonate derivatives of enantiomerically enriched glycidol is described.The enhancement of optical purity by recrystallization was particularly successful for two of these derivatives, glycidyl tosylate and glycidyl 3-nitrobenzenesulfonate, which were obtained in 97 percent ee and 99 percent ee, respectively.Very high regioselectivity was observed in the reactions of these compounds with a variety of nucleophiles, including aryl oxides, Et2AlCN, organometallic reagents, and BH3-NaBH4.The application of this methodology to the synthesis of homochiral β-adrenergic blocking agents and homochiral terminal epoxides is discussed.
