521964-59-0

Basic information

• Product Name: 3-CYCLOPENTENE-1-CARBOXYLIC ACID, 1-[[(1,1-DIMETHYLETHOXY)CARBONYL]AMINO]-, 1,1-DIMETHYLETHYL ESTER
• Synonyms: 3-CYCLOPENTENE-1-CARBOXYLIC ACID, 1-[[(1,1-DIMETHYLETHOXY)CARBONYL]AMINO]-, 1,1-DIMETHYLETHYL ESTER;TERT-BUTYL 1-(BOC-AMINO)-3-CYCLOPENTENE-1-CARBOXYLATE, 97%;1-[[(1,1-Dimethylethoxy)carbonyl]amino]-3-cyclopentene-1-carboxylic acid 1,1-dimethylethyl ester;tert-butyl1-((tert-butoxycarbonyl)amino)cyclopent-3-ene-1-carboxylate
• CAS NO: 521964-59-0
• Molecular Formula: C₁₅H₂₅NO₄
• Molecular Weight: 283.36
• Mol File: 521964-59-0.mol
• Article Data: 3

Chemical Properties

• Melting Point: 86-90 °C
• Boiling Point: 362.26°C at 760 mmHg
• Flash Point: 172.889°C
• Appearance: /
• Density: 1.066g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.489
• CAS DataBase Reference: 3-CYCLOPENTENE-1-CARBOXYLIC ACID, 1-[[(1,1-DIMETHYLETHOXY)CARBONYL]AMINO]-, 1,1-DIMETHYLETHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 3-CYCLOPENTENE-1-CARBOXYLIC ACID, 1-[[(1,1-DIMETHYLETHOXY)CARBONYL]AMINO]-, 1,1-DIMETHYLETHYL ESTER(521964-59-0)
• EPA Substance Registry System: 3-CYCLOPENTENE-1-CARBOXYLIC ACID, 1-[[(1,1-DIMETHYLETHOXY)CARBONYL]AMINO]-, 1,1-DIMETHYLETHYL ESTER(521964-59-0)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 521964-59-0(Hazardous Substances Data)

Usage

General Description

3-CYCLOPENTENE-1-CARBOXYLIC ACID, 1-[[(1,1-DIMETHYLETHOXY)CARBONYL]AMINO]-, 1,1-DIMETHYLETHYL ESTER is a chemical compound with the molecular formula C15H23NO4. It is a 1,1-Dimethylethyl ester derivative of 3-cyclopentene-1-carboxylic acid, which is often used in organic synthesis and pharmaceutical research. 3-CYCLOPENTENE-1-CARBOXYLIC ACID, 1-[[(1,1-DIMETHYLETHOXY)CARBONYL]AMINO]-, 1,1-DIMETHYLETHYL ESTER is known for its potential use as an intermediate in the production of various pharmaceuticals and agrochemicals. It is important to handle this compound with caution and follow proper safety protocols when working with it in a laboratory setting.

InChI:InChI=1/C15H25NO4/c1-13(2,3)19-11(17)15(9-7-8-10-15)16-12(18)20-14(4,5)6/h7-8H,9-10H2,1-6H3,(H,16,18)

Upstream product

• 635318-64-8 1-(isocyanate)-1-(tert-butoxycarbonyl)cyclopent-3-ene 
• 865-47-4 potassium tert-butylate 
• 635318-63-7 1-(acyl-azide)-1-(tert-butoxycarbonyl)cyclopent-3-ene 
• 635318-62-6 1-(chlorocarbonyl)-1-(tert-butoxycarbonyl)cyclopent-3-ene 
• 635318-61-5 3-cyclopentene-1,1-dicarboxylic acid mono(1,1-dimethylethyl) ester 
• 42726-73-8 methyl t-butyl malonate 
• 75-65-0 tert-butyl alcohol 

Downstream Products

• 635318-02-4 (1α,3β,5α)-3-[[(1,1-dimethylethoxy)carbonyl]amino]-6-oxabicyclo[3.1.0]hexane-3-carboxylic acid 1,1-dimethylethyl ester 
• 931396-15-5 (1S,3S,5R)-3-(tert-butoxycarbonylamino)-3-(tert-butoxycarbonyl)-6-oxabicyclo[3.1.O]hexane 

Relevant articles and documents

Facile preparation of tert-butyl 1-tert-butoxycarbonylaminocyclopent-3- enecarboxylate from inexpensive starting materials

1,5-C,C-Cycloalkylation of tert-butyl acetoacetate (1) with cis-1,4-dichloro-2-butene (2) followed by the haloform reaction of the product in NaOH solution and subsequent Curtius degradation in tert-butyl alcohol furnished tert-butyl 1-tert-butoxycarbonyl

PRODRUGS OF EXCITATORY AMINO ACIDS

This invention relates to synthetic excitatory amino acid prodrugs and processes for their preparation. The invention further relates to methods of using, and pharmaceutical compositions comprising, the compounds for the treatment of neurological disorder