121929-88-2

Basic information

• Product Name: (S)-N-(2-benzyloxyacetyl)-4-isopropyl-1,3-thiazolidine-2-thione
• Synonyms: (S)-N-(2-benzyloxyacetyl)-4-isopropyl-1,3-thiazolidine-2-thione
• CAS NO: 121929-88-2
• Molecular Weight: 309.453
• Mol File: 121929-88-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (S)-N-(2-benzyloxyacetyl)-4-isopropyl-1,3-thiazolidine-2-thione(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-N-(2-benzyloxyacetyl)-4-isopropyl-1,3-thiazolidine-2-thione(121929-88-2)
• EPA Substance Registry System: (S)-N-(2-benzyloxyacetyl)-4-isopropyl-1,3-thiazolidine-2-thione(121929-88-2)

Safety Data

• Hazardous Substances Data: 121929-88-2(Hazardous Substances Data)

Upstream product

• 19810-31-2 Benzyloxyacetyl chloride 
• 76186-04-4 (S)-4-isopropylthiazolidine-2-thione 
• 110199-16-1 4(R)-isopropyl-1,3-thiazolidine-2-thione 

Downstream Products

• 132288-50-7 3-(2-(1-methyl-5-oxo-2-pyrrolidinyl)(benzyloxy)acetyl)-4(R)-isopropyl-1,3-thiazolidine-2-thione 
• 121929-85-9 3-(2(S)-(5-oxo-2(R)-pyrrolidinyl)(benzyloxy)acetyl)-4(R)-isopropyl-1,3-thiazolidine-2-thione 

Relevant articles and documents

Direct anti Glycolate Aldol Reaction of Protected Chiral N-Hydroxyacetyl Thiazolidinethiones with Acetals Catalyzed by a Nickel(II) Complex

The direct and stereocontrolled addition of (S)-4-isopropyl-N-(2-pivaloyloxyacetyl)-1,3-thiazolidine-2-thione to dialkyl acetals of aromatic and α,β-unsaturated aldehydes catalyzed by 2.5–5 mol-% of a nickel(II) complex permits the synthesis of diastereom

Highly diastereoselective alkylation of chiral tin(II) enolates onto cyclic acyl imines. An efficient assymetric synthesis of bicyclic alkaloids bearing a nitrogen atom ring juncture

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