135273-88-0

Basic information

• Product Name: <1S<1S<3S(E),4S>>>-benzyl 1-<1-<(3-hex-1-enyl-1-2-oxo-4-oxetanyl),ethyl hexyloxycarbonyl>21-methylpropylcarbamate>
• Synonyms: <1S<1S<3S(E),4S>>>-benzyl 1-<1-<(3-hex-1-enyl-1-2-oxo-4-oxetanyl),ethyl hexyloxycarbonyl>21-methylpropylcarbamate>
• CAS NO: 135273-88-0
• Molecular Weight: 501.664
• Mol File: 135273-88-0.mol

Chemical Properties

• CAS DataBase Reference: <1S<1S<3S(E),4S>>>-benzyl 1-<1-<(3-hex-1-enyl-1-2-oxo-4-oxetanyl),ethyl hexyloxycarbonyl>21-methylpropylcarbamate>(CAS DataBase Reference)
• NIST Chemistry Reference: <1S<1S<3S(E),4S>>>-benzyl 1-<1-<(3-hex-1-enyl-1-2-oxo-4-oxetanyl),ethyl hexyloxycarbonyl>21-methylpropylcarbamate>(135273-88-0)
• EPA Substance Registry System: <1S<1S<3S(E),4S>>>-benzyl 1-<1-<(3-hex-1-enyl-1-2-oxo-4-oxetanyl),ethyl hexyloxycarbonyl>21-methylpropylcarbamate>(135273-88-0)

Safety Data

• Hazardous Substances Data: 135273-88-0(Hazardous Substances Data)

Upstream product

• 1149-26-4 (S)-N-(benzyloxycarbonyl)valine 
• 135273-87-9 <3S(E),4S(S)>-3-hex-1-enyl-4-(2-hydroxyheptyl)-2-oxetanone 
• 135273-86-8 <αS,2S,3R(E)>-3-hex-1-enyl-α-pentyl-2-oxirane ethanol 
• 135273-83-5 4-pentyl-1,3,2-dioxathiolane-2,2-dioxide 
• 135273-85-7 (6S,8Z,10E)-8,10-pentadecadien-6-ol 
• 135273-84-6 (6S,10E)-pentadecen-8-yne-6-ol 
• 107148-34-5 (E)-silane 
• 61228-98-6 (S)-2,2-Dimethyl-4-((Z)-pent-1-enyl)-[1,3]dioxolane 
• 61228-99-7 (S)-(+)-2,2-dimethyl-4-pentyl-1,3-dioxolane 
• 16644-98-7 (E)-1-iodohexene 

Downstream Products

• 113276-96-3 valilactone 

Relevant articles and documents

The Use of ?-Allyltricarbonyliron Lactone Complexes in the Synthesis of the β-Lactone Esterase Inhibitor (-)-Valilactone.

A concise synthesis of the β-lactone esterase inhibitor valilactone (2) is reported.This synthesis employs the stereoselective preparation of a ?-allyltricarbonyliron lactone complex (7) that on oxidation with ceric ammonium nitrate, affords an appropriat

Synthesis of the β-lactone esterase inhibitor valilactone using πallyltricarbonyliron lactone complexes

Synthesis of the esterase inhibitor valilactone (1) is reported employing the oxidation of π-allyltricarbonyliron lactone complexes with ceric ammonium nitrate to afford the inherent β-lactone ring.