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  2. (4R)-4-T-Butyl-1,2,3-oxathiazolidine-2,2-dioxide-3-carboxylic acid t-butyl ester

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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)-

(4R)-4-T-Butyl-1,2,3-oxathiazolidine-2,2-dioxide-3-carboxylic acid t-butyl ester

O=C(N1[C@@H](COS1(=O)=O)C(C)(C)C)OC(C)(C)C Request for Quotation
Chemical Name: (4R)-4-T-Butyl-1,2,3-oxathiazolidine-2,2-dioxide-3-carboxylic acid t-butyl ester
CAS Number: 1313705-92-8
Product Number: AG009F62(AGN-PC-0WQX4L)
Synonyms:
MDL No: MFCD17018786
Molecular Formula: C11H21NO5S
Molecular Weight: 279.3531

Identification/Properties

Computed Properties
Molecular Weight:
279.351g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
279.114g/mol
Monoisotopic Mass:
279.114g/mol
Topological Polar Surface Area:
81.3A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
424
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


(R)-tert-Butyl 4-(tert-butyl)-1,2,3-oxathiazolidine-3-carboxylate 2,2-dioxide is a versatile compound widely used in chemical synthesis due to its unique structural properties and reactivity. This compound is commonly employed as a chiral building block in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Its asymmetric nature allows for the creation of enantiopure molecules, making it an essential tool in the production of optically active compounds. In addition, (R)-tert-Butyl 4-(tert-butyl)-1,2,3-oxathiazolidine-3-carboxylate 2,2-dioxide is known for its stability under various reaction conditions, making it a reliable reagent for complex chemical transformations. Chemists utilize this compound in the development of efficient synthetic routes, enabling the construction of intricate molecular structures with high precision and control.