5732-02-5

Basic information

• Product Name: 2-({3-[(1-methylethoxy)carbonyl]-4,5,6,7-tetrahydro-1-benzothiophen-2-yl}amino)-2-oxoethyl 2-methylquinoline-4-carboxylate
• CAS NO: 5732-02-5
• Molecular Formula: C₁₂H₂₂
• Molecular Weight: 466.5493
• Mol File: 5732-02-5.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 711.1°C at 760 mmHg
• Flash Point: 383.8°C
• Density: 1.31g/cm³
• Vapor Pressure: 4.56E-20mmHg at 25°C
• Refractive Index: 1.643
• CAS DataBase Reference: 2-({3-[(1-methylethoxy)carbonyl]-4,5,6,7-tetrahydro-1-benzothiophen-2-yl}amino)-2-oxoethyl 2-methylquinoline-4-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-({3-[(1-methylethoxy)carbonyl]-4,5,6,7-tetrahydro-1-benzothiophen-2-yl}amino)-2-oxoethyl 2-methylquinoline-4-carboxylate(5732-02-5)
• EPA Substance Registry System: 2-({3-[(1-methylethoxy)carbonyl]-4,5,6,7-tetrahydro-1-benzothiophen-2-yl}amino)-2-oxoethyl 2-methylquinoline-4-carboxylate(5732-02-5)

Safety Data

• Hazardous Substances Data: 5732-02-5(Hazardous Substances Data)

Upstream product

• 5456-34-8 1-acetoxy-3-acetoxymethyl-undecane 
• 111-85-3 n-chlorooctane 
• 32657-89-9 1,3-butadien-2-ylmagnesium chloride 
• 629-27-6 1-Iodooctane 
• 111-83-1 1-bromo-octane 
• 58625-78-8 diethyl 1-methylene-2-propenyl phosphate 
• 17049-49-9 octylmagnesium bromide 
• 3386-35-4 1-octyl p-toluenesulfonate 
• 79240-14-5 3-hydroxymethyl-3-tolylsulfonylundeca-1-ene 
• 629-06-1 1-Chloroheptane 
• 78-79-5 isoprene 
• 629-04-9 1-Bromoheptane 
• 215585-83-4 1-octyl-1-cyclobutene 
• 72195-48-3 1-methyl-4-(undec-1-en-3-ylsulfonyl)benzene 

Downstream Products

• 112069-42-8 2-Methoxymethyl-5-octyl-cyclohexa-1,4-dienecarboxylic acid methyl ester 
• 112069-41-7 2-Methoxymethyl-4-octyl-cyclohexa-1,4-dienecarboxylic acid methyl ester 
• 71138-64-2 3-methyleneundecane 
• 18435-37-5 3-methyl-1-undecene 
• 112069-44-0 2-Methyl-5-octyl-cyclohexa-1,4-dienecarboxylic acid methyl ester 
• 112069-43-9 2-Methyl-4-octyl-cyclohexa-1,4-dienecarboxylic acid methyl ester 
• 102464-03-9 (+/-)-4-octyl-cyclohex-4-ene-1r,2c-dicarboxylic acid diethyl ester 
• 102376-15-8 (+/-)-4ξ-octyl-cyclohexane-1r,2c-dicarboxylic acid diethyl ester 
• 23381-93-3 3-methylundec-2-ene 

Relevant articles and documents

A Silyl Substituent Can Dictate a Concerted Electrocyclic Pathway: Inward Torquoselectivity in the Ring Opening of 3-Silyl-1-cyclobutene

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Method for preparing neophytadiene compounds from fatty acid

The invention relates to a method for preparing neophytadiene compounds from fatty acid. The method comprises the following steps: firstly preparing lipid-containing ketene from fatty acid in two ways, namely a way a comprising the steps of dehydrogenizing the fatty acid by a deprotonation reagent and then reacting with a vinyl Grignard reagent or vinyl lithium to generate ketene compounds, and a way b comprising steps of activating the fatty acid by carbodiimide reagents, then reacting with dialkyl hydroxylamine or hydrochloride thereof to generate N-alkoxy amide compounds (Weinreb amides) and then reacting with the vinyl Grignard reagent or vinyl lithium to generate the ketene compounds; and finally carrying out reaction on the ketene compounds and an olefination reaction reagent to generate the neophytadiene compounds.

Efficient preparation of terminal conjugated dienes by coupling of dienol phosphates with grignard reagents under iron catalysis

(Chemical Equation Presented) An efficient new route to prepare stereoselectively terminal conjugated dienes by coupling Grignard reagents and dienol phosphates in the presence of Fe(acac)3 is described. The synthetic utility of this new iron-catalyzed procedure is illustrated by the synthesis of the pheromone of Diparopsis castanea according to a very expeditious strategy.