1128-00-3

Basic information

• Product Name: 2-AMINO-CYCLOHEX-1-ENECARBOXYLIC ACID ETHYL ESTER
• Synonyms: ETHYL-(2-AMINOCYCLOHEX-1-EN-1-CARBOXYLAT);ETHYL 2-AMINOCYCLOHEX-1-ENE-1-CARBOXYLATE;ETHYL 2-AMINO-1-CYCLOHEXENE-1-CARBOXYLATE;2-AMINO-CYCLOHEX-1-ENECARBOXYLIC ACID ETHYL ESTER;Ethyl 2-amino-1-cyclohexene-1-carboxylate,98%;2-Amino-1-cyclohexenecarboxylic acid ethyl ester;1-Cyclohexene-1-carboxylicacid, 2-aMino-, ethyl ester;Ethyl 2-aMinocyclohex-1-enecarboxylate
• CAS NO: 1128-00-3
• Molecular Formula: C₉H₁₅NO₂
• Molecular Weight: 169.22
• Mol File: 1128-00-3.mol
• Article Data: 13

Chemical Properties

• Melting Point: 70-74 °C
• Boiling Point: 298.52°C (rough estimate)
• Flash Point: 129.3 ºC
• Appearance: White to light yellow/Crystals or Crystalline Powder
• Density: 1.0873 (rough estimate)
• Vapor Pressure: 0.00211mmHg at 25°C
• Refractive Index: 1.4580 (estimate)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• PKA: 6.97±0.20(Predicted)
• CAS DataBase Reference: 2-AMINO-CYCLOHEX-1-ENECARBOXYLIC ACID ETHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 2-AMINO-CYCLOHEX-1-ENECARBOXYLIC ACID ETHYL ESTER(1128-00-3)
• EPA Substance Registry System: 2-AMINO-CYCLOHEX-1-ENECARBOXYLIC ACID ETHYL ESTER(1128-00-3)

Safety Data

• Safety Statements: 24/25
• Hazardous Substances Data: 1128-00-3(Hazardous Substances Data)

Usage

Chemical Properties

white to light yellow crystals or

InChI:InChI=1/C9H15NO2/c1-2-12-9(11)7-5-3-4-6-8(7)10/h7,10H,2-6H2,1H3/b10-8+/t7-/m1/s1

Upstream product

• 1655-07-8 ethyl 2-oxocyclohexane carboxylate 
• 7664-41-7 ammonia 
• 6280-87-1 δ-chlorovaleronitrile 
• 105-36-2 ethyl bromoacetate 
• 460356-12-1 methanesulfonic acid 4-cyano-butyl ester 

Downstream Products

• 1436-60-8 ethyl cis-2-amino-1-cyclohexanecarboxylate 
• 1005269-52-2 2,2'-imino-bis-cyclohexanecarboxylic acid diethyl ester 
• 100870-02-8 3-phenyl-2-thioxo-2,3,5,6,7,8-hexahydro-1H-quinazolin-4-one 
• 56517-53-4 2,4-dihydroxy-5,6,7,8-tetrahydro-quinoline-3-carboxylic acid ethyl ester 
• 52903-71-6 1-hydroxy-3-oxo-2,3,5,6,7,8-hexahydro-isoquinoline-4-carbonitrile 
• 64162-07-8 2-amino-cyclohexanecarboxylic acid ethyl ester 
• 55788-88-0 2-(4-Cyano-benzoylamino)-cyclohex-1-enecarboxylic acid ethyl ester 
• 34170-20-2 ethyl 2-benzoylaminocyclohexene-1-carboxylate 
• 1194701-70-6 2,2-(1'-Ethoxycarbonyl-pentamethylen)-thiazolidon-(4) 
• 55788-87-9 2-(4-Bromo-benzoylamino)-cyclohex-1-enecarboxylic acid ethyl ester 
• 79359-51-6 7,9,10,12-Tetrahydro-8H-5-oxa-12-aza-chrysene-6,11-dione 
• 107154-15-4 2-thioxo-3-p-tolyl-2,3,5,6,7,8-hexahydro-1H-quinazolin-4-one 
• 173277-79-7 2-(acetylamino)cyclohex-1-enecarboxylic acid ethyl ester 
• 56517-59-0 5,6,7,8-tetrahydro-4-hydroxy-2(1H)-quinolinone 

Relevant articles and documents

4-hydroxy-2-quinolones. 95. Synthesis, structure, and antitubercular properties of hetarylamides of 4-hydroxy-2-oxo-1,2,5,6,7,8-hexahydroquinoline-3- carboxylic acid

The optimal conditions for obtaining hetarylamides of 4-hydroxy-2-oxo-1,2, 5,6,7,8-hexahydroquinoline-3-carboxylic acid are suggested on the basis of derivatographic investigations. The 1H NMR spectra of the synthesized compounds, their spatial

Synthesis of oxazolidin-2-ones and imidazolidin-2-ones directly from 1,3-diols or 3-amino alcohols using iodobenzene dichloride and sodium azide

A general and efficient method for the synthesis of oxazolidin-2-ones and imidazolidin-2-ones directly from 1,3-diols and 3-amino alcohols has been developed using the same reagent combination of iodobenzene dichloride (PhICl2) and sodium azide (NaN3).

An unusual boron tribromide-mediated, one-pot bromination/cyclization reaction. Application to the synthesis of a highly strained cyclopenta[1,3] cyclopropa[1,2-b]pyrrolizin-8-one

Performing Jefford's cyclization of ethyl 2-pyrrol-1-ylcyclohex-2-ene-1- carboxylate (5) using boron tribromide in refluxing dichloromethane led to a trans-cis bromopyrrolohydrindolone 7 whose debromination in alkaline medium afforded a highly strained cy