| Identification | Back Directory | [Name]
(2R,4R)-(+)-4-ISOPROPYL-2-P-TOLUENE-4,5-DIHYDRO-(1,2LAMBDA6,3)-OXATHIAZOLE 2-OXIDE | [CAS]
170900-87-5 | [Synonyms]
(2R,4R)-(+)-4-ISOPROPYL-2-(P-TOLYL)-4,5&
(2r,4r)-(+)-4,5-dihydro-4-isopropyl-2-(p-tolyl)-1,2λ4,3-oxathiazole 2-oxide
(2R,4R)-4-ISOPROPYL-2-P-TOLUENE-4,5-DIHYDR O-(1,2LAM(6),3)-OXATHIAZOLE 2-OXIDE98
(2R,4R)-(+)-4-ISOPROPYL-2-P-TOLUENE-4,5-DIHYDRO-(1,2LAMBDA6,3)-OXATHIAZOLE 2-OXIDE
2λ4-1,2,3-Oxathiazole, 4,5-dihydro-4-(1-methylethyl)-2-(4-methylphenyl)-, 2-oxide, (2R,4R)- (9CI) | [Molecular Formula]
C12H17NO2S | [MDL Number]
MFCD08275413 | [MOL File]
170900-87-5.mol | [Molecular Weight]
239.33 |
| Chemical Properties | Back Directory | [Melting point ]
82-86 °C (lit.) | [Boiling point ]
336.8±35.0 °C(Predicted) | [density ]
1.19±0.1 g/cm3(Predicted) | [optical activity]
[α]20/D +85°, c = 1% in chloroform |
| Hazard Information | Back Directory | [Uses]
(2R,4R)-(+)-4,5-Dihydro-4-isopropyl-2-(p-tolyl)-1,2λ4,3-oxathiazole 2-oxide can be used as a precursor for the preparation of alkyl- and 2 alkenyl sulfoximines by reacting with corresponding Grignard reagents. These sulfoximines may also be used as asymmetric d3 building blocks. |
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