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  2. (3S)-Trichloromethyl-cis-tetrahydropyrrolo[1,2-c]oxazol-1-one

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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)-

(3S)-Trichloromethyl-cis-tetrahydropyrrolo[1,2-c]oxazol-1-one

O=C1O[C@H](N2[C@@H]1CCC2)C(Cl)(Cl)Cl Request for Quotation
Chemical Name: (3S)-Trichloromethyl-cis-tetrahydropyrrolo[1,2-c]oxazol-1-one
CAS Number: 1330286-50-4
Product Number: AG009WRN(AGN-PC-0WA24O)
Synonyms:
MDL No:
Molecular Formula: C7H8Cl3NO2
Molecular Weight: 244.5029

Identification/Properties

Computed Properties
Molecular Weight:
244.496g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
242.962g/mol
Monoisotopic Mass:
242.962g/mol
Topological Polar Surface Area:
29.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
240
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
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


(3S,7aR)-Tetrahydro-3-(trichloromethyl)-1H,3H-pyrrolo[1,2-c]oxazol-1-one is a versatile compound widely used in chemical synthesis. Its unique structure containing a trichloromethyl group makes it a valuable building block in organic chemistry. This compound is commonly employed in the synthesis of complex molecules, especially in the pharmaceutical industry. The trichloromethyl group can participate in various chemical reactions, such as nucleophilic substitution and cross-coupling reactions, allowing for the efficient construction of carbon-carbon and carbon-heteroatom bonds. Additionally, the pyrrolooxazolone scaffold provides rigidity and stereochemical control, making it a valuable tool in the design and synthesis of bioactive compounds.