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1203507-02-1

1203507-02-1 Structure

1203507-02-1 Structure
IdentificationBack Directory
[Name]

(2S,3R)-(+)-3-Isopropyl-2-phenyl-3,4-dihydro-2H-pyrimido[2,1-b][1,3]benzothiazole98+%
[CAS]

1203507-02-1
[Synonyms]

(2S,3R)-3,4-Dihydro-3-isopropyl-2-phenyl-2H-pyrimido[2,1-b]benzothiazole
(2S,3R)-(+)-3-Isopropyl-2-phenyl-3,4-dihydro-2H-pyrimido[2,1-b][1,3]benzothiazole98+%
(2R,3S)-(-)-3,4-Dihydro-3-(i-propyl)-2-phenyl-2H-pyrimido[2,1-b]benzothiazole, min. 98% HyperBTM
(2S,3R)-3,4-Dihydro-3-isopropyl-2-phenyl-2H-pyrimido[2,1-b]benzothiazole
[Molecular Formula]

C19H20N2S
[MDL Number]

MFCD28411847
Chemical PropertiesBack Directory
[Melting point ]

197.0 to 201.0 °C
[alpha ]

+288.4°
[form ]

Powder
[color ]

white
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P280-P301+P312-P302+P352-P305+P351+P338
Questions And AnswerBack Directory
[Reaction]

  1. Isothiourea-mediated intermolecular Michael addition-lactonisation.
  2. Isothiourea-mediated, asymmetric, Michael-lactonisation of CF3 – enones.
  3. α-Functioalisation of 3-alkenoic acids.
  4. Isothiourea-catalyzed α-amination of carboxylic acids.
  5. Isothiourea-catalyzed O- to C- carboxyl transfer of furanyl carbonates.
  6. Isothiourea-catalyzed kinetic resolution of secondary alcohols.
  7. Isothiourea-catalyzed α-amination of carboxylic acidswith N-aryl-N-aroyldiazene. 
Reactions of 1203507-02-1_1
Reactions of 1203507-02-1_2
Reactions of 1203507-02-1_3
Spectrum DetailBack Directory
[Spectrum Detail]

(2S,3R)-(+)-3-Isopropyl-2-phenyl-3,4-dihydro-2H-pyrimido[2,1-b][1,3]benzothiazole98+%(1203507-02-1)1HNMR
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