58774-06-4

Basic information

• Product Name: triethyl 3-cyanopentane-1,3,5-tricarboxylate
• CAS NO: 58774-06-4
• Molecular Formula: C₁₅H₂₃NO₆
• Molecular Weight: 313.3462
• Mol File: 58774-06-4.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 419.4°C at 760 mmHg
• Flash Point: 183.4°C
• Density: 1.119g/cm³
• Vapor Pressure: 3.04E-07mmHg at 25°C
• Refractive Index: 1.46
• CAS DataBase Reference: triethyl 3-cyanopentane-1,3,5-tricarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: triethyl 3-cyanopentane-1,3,5-tricarboxylate(58774-06-4)
• EPA Substance Registry System: triethyl 3-cyanopentane-1,3,5-tricarboxylate(58774-06-4)

Safety Data

• Hazardous Substances Data: 58774-06-4(Hazardous Substances Data)

Usage

General Description

Triethyl 3-cyanopentane-1,3,5-tricarboxylate is a chemical compound with the molecular formula C17H23NO6. It is an ester derived from pentane-1,3,5-tricarboxylic acid, containing three ethyl groups and a cyano group attached to the carbon chain. triethyl 3-cyanopentane-1,3,5-tricarboxylate is commonly used in organic synthesis as a reagent for the preparation of various functionalized molecules. It is also used in the pharmaceutical industry for the synthesis of potential drug candidates due to its ability to functionalize and modify molecules with multiple ester groups. Additionally, triethyl 3-cyanopentane-1,3,5-tricarboxylate is utilized in the production of specialty chemicals and as a building block for the creation of complex organic compounds.

Upstream product

• 18852-51-2 sodium cyanoacetic acid ethyl ester 
• 623-71-2 ethyl 3-chloropropanoate 
• 105-56-6 ethyl 2-cyanoacetate 
• 140-88-5 ethyl acrylate 
• 539-74-2 Ethyl 3-bromopropionate 
• 7251-97-0 diethyl 2-cyanoglutarate 
• 6414-69-3 ethyl 3-iodopropanoate 

Downstream Products

• 6940-58-5 pentane-1,3,5-tricarboxylic acid 
• 58774-04-2 ethyl 1-cyano-4-oxocyclohexanecarboxylate 

Relevant articles and documents

A simple and highly efficient procedure for construction of quaternary carbons centers by tributylphosphine catalyzed bis-Michael addition

The tributylphosphine-catalyzed bis-Michael addition reaction of various kinds of α,β-unsaturated carbonyl compounds with active methylenes is described. This is a convenient and rapid method for generating quaternary carbons centers and useful procedure for the synthesis of branched core and highly substituted trans cyclohexanones. All the reactions were completed in 60 min and afford the corresponding products in excellent yields.

1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU): A powerful catalyst for the Michael addition reaction of β-ketoesters to acrylates and enones

The Michael addition reaction of 1,3-dicarbonyl compounds and enones was carried out in the presence of a catalytic amount of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) in ethanol under the mild reaction condition furnished Michael adducts in excellent yield.

1,5,7-triazabicyclo[4.4.0]dec-5-ene immobilized in MCM-41: A strongly basic porous catalyst

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