194034-43-0

Basic information

• Product Name: Carbamic acid, [2-[(4S)-5-oxo-2,2-bis(trifluoromethyl)-1,3-dioxolan-4-yl]ethyl]-, phenylmethyl ester
• CAS NO: 194034-43-0
• Molecular Formula: C15H13F6NO5
• Molecular Weight: 401.262
• Mol File: 194034-43-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Carbamic acid, [2-[(4S)-5-oxo-2,2-bis(trifluoromethyl)-1,3-dioxolan-4-yl]ethyl]-, phenylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, [2-[(4S)-5-oxo-2,2-bis(trifluoromethyl)-1,3-dioxolan-4-yl]ethyl]-, phenylmethyl ester(194034-43-0)
• EPA Substance Registry System: Carbamic acid, [2-[(4S)-5-oxo-2,2-bis(trifluoromethyl)-1,3-dioxolan-4-yl]ethyl]-, phenylmethyl ester(194034-43-0)

Safety Data

• Hazardous Substances Data: 194034-43-0(Hazardous Substances Data)

Upstream product

• 603960-96-9 tert-butyl 3-[(5S)-2,2-bis(trifluoromethyl)-4-oxo-1,3-dioxolan-5-yl]propionate 
• 194034-38-3 (5S)-5-(3-diazo-2-oxopropyl)-2,2-bis-(trifluoromethyl)-1,3-dioxolan-4-one 
• 194034-40-7 3-[(5S)-2,2-bis(trifluoromethyl)-4-oxo-1,3-dioxolan-5-yl]propionyl chloride 
• 172540-28-2 ((5S)-2,2-bis-(trifluoromethyl)-4-oxo-1,3-dioxolan-5-yl)-acetyl chloride 
• 172540-27-1 [(5S)-2,2-Bis(trifluoromethyl)-4-oxo-1,3-dioxolan-5-yl] acetic acid 
• 183671-77-4 (5S)-5-(2-isocyanatoethyl)-2,2-bis(trifluoromethyl)-1,3-dioxolan-4-one 
• 100-51-6 benzyl alcohol 

Downstream Products

• 34368-52-0 (S)-3-hydroxypyrrolidin-2-one 

Relevant articles and documents

Suntheses of (3S)-3-hydroxy-2-pyrrolidinone from (S)-malic acid

(S)-Malic acid 2 is transformed into (3S)-3-hydroxy-2-pyrrolidinone (8) using hexafluoroacotone os protecting and activating agent. Two alternative routes were developed; key step of both routes is the intramolecular aminolytic cleavage of the lactone rin

Orthogonally protected, carboxy-activated L-homoisoserine, 2-methyl-L-homoisoserine, and homoisocysteine derivatives. New building blocks for peptide and depsipeptide modification

Starting from L-malic, L-citramalic, and rac. thiomalic acids routes to L-homoisoserine, 2-methyl-L-homoisoserine and rac. homoisocysteine have been developed. The new orthogonally protected and carboxy-activated building blocks are GABA as well as α-hydr