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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

4-(azetidin-3-yl)-1,4-thiazinane 1,1-dioxide

O=S1(=O)CCN(CC1)C1CNC1 Request for Quotation
Chemical Name: 4-(azetidin-3-yl)-1,4-thiazinane 1,1-dioxide
CAS Number: 780732-40-3
Product Number: AG00GIDB(AGN-PC-0D3K05)
Synonyms:
MDL No:
Molecular Formula: C7H14N2O2S
Molecular Weight: 190.26326

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(Azetidin-3-yl)thiomorpholine 1,1-dioxide is a versatile chemical compound widely utilized in chemical synthesis processes. This unique compound serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its structural features make it an essential intermediate in the development of complex molecules, particularly in the pharmaceutical industry. The presence of the azetidine ring and thiomorpholine moiety in its structure imparts distinct reactivity and selectivity, making it valuable for the synthesis of bioactive compounds and functional materials. In organic synthesis, 4-(Azetidin-3-yl)thiomorpholine 1,1-dioxide acts as a key reagent for introducing specific functionalities, enhancing molecular diversity, and facilitating the formation of intricate molecular frameworks. Its application in chemical transformations such as ring-opening reactions, nucleophilic additions, and cross-coupling reactions highlights its significance as a versatile tool for synthetic chemists seeking to access novel chemical entities with potential biological activities.