1166394-91-7

Basic information

• Product Name: (R)-tert-butyl 4-(4-hydroxybutyl)-2,2-diMethyloxazolidine-3-carboxylate
• Synonyms: (R)-tert-butyl 4-(4-hydroxybutyl)-2,2-diMethyloxazolidine-3-carboxylate
• CAS NO: 1166394-91-7
• Molecular Formula: C14H27NO4
• Molecular Weight: 273.36848
• Mol File: 1166394-91-7.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: (R)-tert-butyl 4-(4-hydroxybutyl)-2,2-diMethyloxazolidine-3-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-tert-butyl 4-(4-hydroxybutyl)-2,2-diMethyloxazolidine-3-carboxylate(1166394-91-7)
• EPA Substance Registry System: (R)-tert-butyl 4-(4-hydroxybutyl)-2,2-diMethyloxazolidine-3-carboxylate(1166394-91-7)

Safety Data

• Hazardous Substances Data: 1166394-91-7(Hazardous Substances Data)

Usage

General Description

(R)-tert-butyl 4-(4-hydroxybutyl)-2,2-diMethyloxazolidine-3-carboxylate is a chemical compound with potential applications in the pharmaceutical industry. It is a derivative of oxazolidine, a heterocyclic compound containing both nitrogen and oxygen atoms in the ring structure. This specific compound has a tert-butyl group and a hydroxybutyl group attached to the oxazolidine ring, as well as a carboxylate group. The presence of these functional groups makes it a versatile compound for potential drug design and synthesis. Its stereochemistry and structural features make it a valuable candidate for the development of new pharmaceuticals targeting specific biological pathways. Further research and testing are needed to explore the full potential of this compound in the medical field.

Upstream product

• 905718-71-0 (S,E)-tert-butyl-4-(4-ethoxy-4-oxobut-2-enyl)-2,2-dimethyloxazolidine-3-carboxylate 
• 147959-19-1 (4S)-2,2-dimethyl-3-(t-butoxycarbonyl)-4-(formylmethyl)-1,3-oxazolidine 
• 77-76-9 2,2-dimethoxy-propane 
• 213176-18-2 tert-butyl [(1S)-5-hydroxy-1-(hydroxymethyl)pentyl]carbamate 

Downstream Products

• 1079209-05-4 tert-butyl (4S)-4-[4-(benzyloxy)butyl]-2,2-dimethyl-1,3-oxazolidine-3-carboxylate 
• 1257405-71-2 C₃₀H₄₅NO₄Si 

Relevant articles and documents

Synthesis of 2-aminosuberic acid derivatives as components of some histone deacetylase inhibiting cyclic tetrapeptides

A new synthesis of the important amino acid 2-aminosuberic acid from aspartic acid is reported. The methodology involves the alternate preparation of (S)-2-aminohept-6-enoate ester as a building block and its diversification through a cross-metathesis reaction to prepare the title compounds. The utility of the protocol is demonstrated through the preparation of three suberic acid derivatives of relevance to the design and the synthesis of peptides of biological relevance.

PROCESS FOR PRODUCTION OF 4-(SUBSTITUTED PHENYL)HEXAHYDROPYRIDOY2,1-C¨Y1,4¨OXAZIN-6-ONE

4-(Substituted phenyl)hexahydropyrido[2,1-c][1,4]oxazin-6-one represented by formula (I) or a salt thereof is useful as an intermediate for the production of a bicyclic cinnamide compound which is an Aβ production inhibitor. 4-(Substituted phenyl)hexahydropyrido[2,1-c][1,4]oxazin-6-one or the salt thereof can be produced in an industrially advantageous manner by subjecting a compound represented by formula (II) or a salt thereof to an intramolecular condensation reaction.