2594-20-9

Basic information

• Product Name: ethyl propan-2-ylcarbamate
• CAS NO: 2594-20-9
• Molecular Formula: C₆H₁₃NO₂
• Molecular Weight: 131.1729
• Mol File: 2594-20-9.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 183.8°C at 760 mmHg
• Flash Point: 65°C
• Density: 0.935g/cm³
• Vapor Pressure: 0.756mmHg at 25°C
• Refractive Index: 1.415
• CAS DataBase Reference: ethyl propan-2-ylcarbamate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl propan-2-ylcarbamate(2594-20-9)
• EPA Substance Registry System: ethyl propan-2-ylcarbamate(2594-20-9)

Safety Data

• Hazardous Substances Data: 2594-20-9(Hazardous Substances Data)

Usage

General Description

Ethyl propan-2-ylcarbamate, also known as EPCI, is a chemical compound derived from carbamic acid and is used primarily as a pesticide. It is used to control a wide range of insects and pests in agricultural and horticultural settings. EPCI works by disrupting the normal function of the nervous systems of insects, leading to paralysis and eventual death. It is often applied as a spray or dust and has a low toxicity to mammals, making it a popular choice for insect control. However, it is important to handle EPCI with care and follow safety guidelines to prevent exposure and potential harm to humans and animals.

Upstream product

• 75-35-4 1,1-Dichloroethylene 
• 64-17-5 ethanol 
• 904294-61-7 3-amino-4-pyridinylcarbamic acid ethyl ester 
• 75-31-0 isopropylamine 
• 126-98-7 methacrylonitrile 
• 80-62-6 methacrylic acid methyl ester 
• 292638-85-8 acrylic acid methyl ester 
• 107-13-1 acrylonitrile 
• 19092-08-1 N-Methyl-N-nitrourethan 
• 541-41-3 chloroformic acid ethyl ester 
• 1795-48-8 Isopropyl isocyanate 
• 1008-89-5 2-phenylpyridine 
• 104388-02-5 N-isopropyl-3,3-bisethoxycarbonyl oxaziridine 

Downstream Products

• 62261-05-6 isopropyl-nitro-carbamic acid ethyl ester 
• 1795-48-8 Isopropyl isocyanate 
• 4747-21-1 N-methylpropan-2-amine 

Relevant articles and documents

Continuous Flow Synthesis of Urea-Containing Compound Libraries Based on the Piperidin-4-one Scaffold

The advantages of performing reactions in continuous flow vs. the classic batch processes render flow chemistry a suitable technique for library synthesis. Inspired by our recent work to create fluorine-containing nitrogen heterocycles and by the potentia

N-acyl and N-alkoxycarbonyl derivatives of 1H-1,2,3-triazolo-[4,5-c] pyridine; preparation and application

The N-acylating and N-alkoxycarbonylation ability of the N-substituted 1,2,3-triazolo[4,5-c]pyridines 1a-e have been investigated. The alkoxycarbonyl triazolopyridine derivatives (1c-e) were readily prepared in 81-96% yield (the corresponding tetrafluoroborate > 95%). Triazolo[4,5-c]pyridine (1) has been shown to work as a good leaving group by the formation of amido- and carbamate protected derivatives of primary amines. The method was also successful for the N-tert-butoxycarbonyl (N-BOC) protection of the amino acid, phenylalanine. The synthetic transformations are facilitated by the one-pot preparation of 1a-e followed by the direct reaction with the amines or amino acid. The present method thus offers an efficient and convenient protocol for the in situ preparation of triazolopyridine reagents to be used directly for the protection of amines and amino acids. N-Acyl- and N-alkoxycarbonyl triazolopyridines (1a-e) were readily prepared in 4 steps from 4-aminopyridine (4) by amine protection, pyridine nitration, nitro reduction and diazotizations/cyclizations. All reactions offer the advantages of rapid conversions in high yields under very mild conditions.

N-sulfenylated pyrazolines, compositions and use

N-sulfenylated and N-acrylated pyrazoline arthropodicides, compositions containing them and methods for controlling arthropods by applying compounds of the invention to them or to their environment. The pyrazolines are selected from those of Formulae I to III wherein R1, R2, R3, Q, A, B, J, K, Y, m, n and p are as defined in the test: STR1