104805-25-6

Basic information

• Product Name: Benzenepropanethioic acid, b-hydroxy-, S-(1,1-dimethylethyl) ester, (S)-
• CAS NO: 104805-25-6
• Molecular Formula: C13H18O2S
• Molecular Weight: 238.351
• Mol File: 104805-25-6.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: Benzenepropanethioic acid, b-hydroxy-, S-(1,1-dimethylethyl) ester, (S)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenepropanethioic acid, b-hydroxy-, S-(1,1-dimethylethyl) ester, (S)-(104805-25-6)
• EPA Substance Registry System: Benzenepropanethioic acid, b-hydroxy-, S-(1,1-dimethylethyl) ester, (S)-(104805-25-6)

Safety Data

• Hazardous Substances Data: 104805-25-6(Hazardous Substances Data)

Upstream product

• 463-51-4 Ketene 
• 100-52-7 benzaldehyde 
• 16528-55-5 stannous 2-methyl-2-propanethiolate 
• 999-90-6 S-tert-butyl thioacetate 
• 63584-41-8 1-ethylthio-1-(trimethylsiloxy)ethene 
• 63584-47-4 (1-tert-butylsulfanyl-vinyloxy)trimethylsilane 
• 175227-32-4 (S)-3-((R)-1-Methyl-3-oxo-propoxy)-3-phenyl-thiopropionic acid S-tert-butyl ester 
• 79464-76-9 (2S,4R)-4-methyl-2-phenyl-1,3-dioxane 
• 175227-22-2 (S)-3-((R)-3-Hydroxy-1-methyl-propoxy)-3-phenyl-thiopropionic acid S-tert-butyl ester 
• 175227-31-3 (S)-3-((R)-1-Methyl-3-trimethylsilanyloxy-propoxy)-3-phenyl-thiopropionic acid S-tert-butyl ester 

Relevant articles and documents

The E/Z geometry of the enolate component determines face selection of the aldehyde component in chiral diazaborolidine-directed enantioselective aldol coupling

An analysis of the effect of enolate geometry on transition-state energy explains the stereochemistry of aldol reactions of acetate and propionate esters with aldehydes using as reagent the chiral diazaborolidine 1.

Catalytic, enantioselective hetero-Diels-Alder reaction with novel, chiral bis-titanium(IV) catalyst

Our recently designed chiral bis-titanium(IV) catalyst can be successfully utilized for the catalytic enantioselective hetero-Diels-Alder reaction of aldehyde and Danishefsky's diene. The high asymmetric induction is achievable in the case of sterically l

Computerunterstuetztes Design von chiralen Borenolaten: eine neue, hoch enantioselektive Aldolreaktion fuer Thioacetate und Thiopropionate

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