84764-41-0

Basic information

• Product Name: 1H-Isoindole-1,3(2H)-dione, 2-[2-(2-methyl-1,3-dioxolan-2-yl)ethyl]-
• CAS NO: 84764-41-0
• Molecular Formula: C14H15NO4
• Molecular Weight: 261.277
• Mol File: 84764-41-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1H-Isoindole-1,3(2H)-dione, 2-[2-(2-methyl-1,3-dioxolan-2-yl)ethyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Isoindole-1,3(2H)-dione, 2-[2-(2-methyl-1,3-dioxolan-2-yl)ethyl]-(84764-41-0)
• EPA Substance Registry System: 1H-Isoindole-1,3(2H)-dione, 2-[2-(2-methyl-1,3-dioxolan-2-yl)ethyl]-(84764-41-0)

Safety Data

• Hazardous Substances Data: 84764-41-0(Hazardous Substances Data)

Usage

Molecular Structure

A complex structure consisting of an isoindole ring and a 1,3-dione functional group.

Side Chain

A 2-(2-methyl-1,3-dioxolan-2-yl)ethyl side chain attached to the isoindole ring.

Isoindole Ring

A fused bicyclic ring system with one six-membered benzene ring and one five-membered nitrogen-containing ring.

1,3-Dione Functional Group

A functional group consisting of two carbonyl groups (C=O) located at the 1 and 3 positions of the isoindole ring.

2-Methyl-1,3-Dioxolan-2-Yl Group

A 1,3-dioxolan ring with a methyl group attached to the 2 position.

Ethyl Side Chain

A two-carbon alkyl chain (C2H5) connected to the 2-methyl-1,3-dioxolan-2-yl group.

Potential Applications

Possible uses in pharmaceuticals, agrochemicals, and materials science due to its unique structure and properties.

Further Research

Necessary to fully understand the characteristics and potential uses of this chemical compound.

Upstream product

• 136918-14-4 phthalimide 
• 1074-82-4 potassium phtalimide 
• 3783-77-5 N-(3-oxobutyl)phthalimide 
• 107-21-1 ethylene glycol 

Downstream Products

• 109463-92-5 4-(3-methoxybenzylideneamino)butan-2-one ethylene acetal 
• 138489-32-4 C₃₄H₄₃NO₄Se 
• 138489-31-3 C₃₄H₅₃NO₄SSi 
• 138489-36-8 C₂₉H₃₆ClNO₄ 
• 138489-35-7 C₂₉H₃₇NO₅ 
• 104115-60-8 C₃₀H₄₁NO₅ 
• 138489-29-9 C₃₁H₄₅NO₄S 
• 138489-27-7 (1''R+S,7R^*,7aR^*,10aS^*)-(+/-)-Hexahydro-7-(1'',5''-dimethyl-3''-oxohexyl)-7-<3-(phenylmethoxy)propyl>spiroindolizine-2(1H),2'-<1,3>dioxolan>-6(7H)-one 
• 138489-37-9 C₃₀H₃₉NO₄ 
• 104115-49-3 (1''R+S,7R^*,7aR^*,10aS^*)-(+/-)-Hexahydro-7-(1''-methyl-3''-oxobutyl)-7-<3-(phenylmethoxy)propyl>spiroindolizine-2(1H),2'-<1,3>dioxolan>-6(7H)-thione 
• 138602-83-2 (3aS^*,12α,12aα,12bβ)-(+/-)-2,3,6,7,11,12,12a,12b-Octahydro-12-methyl-12a-<3-(phenylmethoxy)propyl>spiropyrido<1,2-a>indole-5(4H),2'-<1,3>dioxolan>-10(1H)-one 
• 104115-52-8 (3aS^*,8aα,12aα,12bβ)-(+/-)-2,3,6,7,8a,9,12a,12b-Octahydro-12-methyl-12a-<3-(phenylmethoxy)propyl>spiropyrido<1,2-a>indole-5(4H),2'-<1,3>dioxolan>-10(1H)-one 
• 138602-84-3 (3aS^*,8aα,12α,12aα,12bβ)-(+/-)-Decahydro-12-methyl-12a-<3-(phenylmethoxy)propyl>spiropyrido<1,2-a>indole-5(4H),2'-<1,3>dioxolan>-10(1H)-one 
• 138489-28-8 (7R^*,7aR^*,10aS^*)-(+/-)-Hexahydro-7-<3-(phenylmethoxy)propyl>spiroindolizine-2(1H),2'-<1,3>thioxolan>-6(7H)-thione 

Relevant articles and documents

Highly Regioselective 5-endo-tet Cyclization of 3,4-Epoxy Amines into 3-Hydroxypyrrolidines Catalyzed by La(OTf)3

Highly regioselective intramolecular aminolysis of 3,4-epoxy amines has been achieved. Key features of this reaction are (1) chemoselective activation of epoxides in the presence of unprotected aliphatic amines in the same molecules by a La(OTf)3 catalyst and (2) excellent regioselectivity for anti-Baldwin 5-endo-tet cyclization. This reaction affords 3-hydroxy-2-alkylpyrrolidines stereospecifically in high yields. DFT calculations revealed that the regioselectivity might be attributed to distortion energies of epoxy amine substrates. The use of this reaction was demonstrated by the first enantioselective synthesis of an antispasmodic agent prifinium bromide.

New efficient synthesis of pyrido[2,3-c] and pyrido[3,2-c]coumarin derivatives

Various substituted pyrido[2,3-c] and pyrido[3,2-c]coumarins are efficiently prepared in three steps from 3- and 4-hydroxycoumarins, respectively and protected β-aminoketones.