51498-33-0

Basic information

• Product Name: 4-AMINO-CYCLOHEXANECARBOXYLIC ACID ETHYL ESTER
• Synonyms: 4-AMINO-CYCLOHEXANECARBOXYLIC ACID ETHYL ESTER;Cyclohexanecarboxylic acid, 4-aMino-, ethyl ester;Ethyl 4-aMinocyclohexanecarboxylate
• CAS NO: 51498-33-0
• Molecular Formula: C₉H₁₇NO₂
• Molecular Weight: 171.238
• Mol File: 51498-33-0.mol
• Article Data: 15

Chemical Properties

• Boiling Point: 235.3°C at 760 mmHg
• Flash Point: 101.5°C
• Appearance: /
• Density: 1.018g/cm³
• Vapor Pressure: 0.0505mmHg at 25°C
• Refractive Index: 1.468
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• PKA: 10.36±0.70(Predicted)
• CAS DataBase Reference: 4-AMINO-CYCLOHEXANECARBOXYLIC ACID ETHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 4-AMINO-CYCLOHEXANECARBOXYLIC ACID ETHYL ESTER(51498-33-0)
• EPA Substance Registry System: 4-AMINO-CYCLOHEXANECARBOXYLIC ACID ETHYL ESTER(51498-33-0)

Safety Data

• Hazardous Substances Data: 51498-33-0(Hazardous Substances Data)

Usage

General Description

4-Amino-Cyclohexanecarboxylic Acid Ethyl Ester is a chemical compound that can be synthesized through various chemical reactions. Its presence as an ethyl ester form signifies that it's a product of esterification, a reaction between carboxylic acid and alcohol. Its structure comprises a cyclohexane ring, characteristic of the cyclohexane series of organic compounds, and an amino group which consists of a basic nitrogen atom with a lone pair. 4-AMINO-CYCLOHEXANECARBOXYLIC ACID ETHYL ESTER may potentially have applications in the field of organic synthesis or drug design, but its specific properties and uses would need to be further explored and evaluated through research and experimentation.

InChI:InChI=1/C9H17NO2/c1-2-12-9(11)7-3-5-8(10)6-4-7/h7-8H,2-6,10H2,1H3

Upstream product

• 1776-53-0 4-aminocyclohexanecarboxylic acid 
• 64-17-5 ethanol 
• 90942-89-5 ethyl 4-(hydroxyimino)cyclohexane-1-carboxylate 
• 94-09-7 p-aminoethylbenzoate 
• 3685-23-2 cis-4-aminocyclohexane-1-carboxylic acid 
• 3618-04-0 4-hydroxycyclohexyl carboxylic acid ethyl ester 
• 17159-79-4 ethyl 4-oxocyclohexane-1-carboxylate 
• 57555-71-2 4-hydroxyimino-cyclohexanecarboxylic acid 
• 150-13-0 4-amino-benzoic acid 

Downstream Products

• 117130-96-8 C₁₁H₂₂ClN₂O₃P 
• 117112-34-2 ethyl N-(N'N'-dimethylamido-N''-cyclohexylamido)-phosphoryl-cis-4-aminocyclohexanecarboxylate 
• 78431-97-7 4-[Bis-(2-chloro-ethyl)-amino]-cyclohexanecarboxylic acid; hydrochloride 
• 78431-94-4 4-[Bis-(2-chloro-ethyl)-amino]-cyclohexanecarboxylic acid ethyl ester; hydrochloride 
• 117112-26-2 ethyl N-(N'N'-dimethylamido-N''-morpholido)phosphoryl-trans-4-aminocyclohexanecarboxylate 
• 117112-25-1 ethyl N-(N'N'-dimethylamido-N''-morpholido)phosphoryl-cis-4-aminocyclohexanecarboxylate 
• 117112-28-4 ethyl N-phosphoryl-cis-4-aminocyclohexanecarboxylate 
• 117112-31-9 ethyl N-phosphoryl-cis-4-aminocyclohexanecarboxylate 
• 3306-69-2 2-aza-bicyclo[2.2.2]octan-3-one 
• 1357918-57-0 (1s,4s)-ethyl 4-((E)-2-(benzoylimino)-6-(piperidin-1-ylmethyl)-2,3-dihydro-1H-benzo[d]imidazol-1-yl)cyclohexanecarboxylate 

Relevant articles and documents

Antibacterial Compounds

The present invention provides a compound of the following formula, salts, racemates, diastereomers, enantiomers, esters, carbamates, phosphates, sulfates, deuterated forms and prodrugs thereof. Also provided is the use of these compounds as antibacterials, compositions comprising them and processes for their manufacture.

ANTIBACTERIAL COMPOUNDS

The present invention provides a compound of the following formula and salts thereof: Also provided is the use of these compounds as antibacterials, compositions comprising them and processes for their manufacture.

Improved ruthenium-catalyzed amination of alcohols with ammonia: Synthesis of diamines and amino esters

Diamination of diols: The first homogeneously catalyzed diaminations of primary and secondary diols with ammonia give the corresponding diamines. Other primary as well as secondary alcohols including hydroxy-substituted esters can also be efficiently converted to primary amines. This atom-efficient and selective amination method proceeds in an ammonia atmosphere without additional hydrogen sources. Copyright