884507-44-2

Basic information

• Product Name: 1-(3-IODOBENZYL)PYRROLIDINE
• Synonyms: 1-(3-IODOBENZYL)PYRROLIDINE;1-(3-Iodobenzyl)pyrrolidine 97%
• CAS NO: 884507-44-2
• Molecular Formula: C₁₁H₁₄IN
• Molecular Weight: 287.14
• Mol File: 884507-44-2.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 305°C at 760 mmHg
• Flash Point: 138.3°C
• Appearance: /
• Density: 1.593g/cm³
• Vapor Pressure: 0.000843mmHg at 25°C
• Refractive Index: 1.629
• CAS DataBase Reference: 1-(3-IODOBENZYL)PYRROLIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3-IODOBENZYL)PYRROLIDINE(884507-44-2)
• EPA Substance Registry System: 1-(3-IODOBENZYL)PYRROLIDINE(884507-44-2)

Safety Data

• Hazard Codes: C
• Hazardous Substances Data: 884507-44-2(Hazardous Substances Data)

Usage

General Description

1-(3-Iodobenzyl)pyrrolidine is a chemical compound that belongs to the class of organic compounds known as pyrrolidines. It contains a pyrrolidine ring with a 3-iodobenzyl group attached to it. This chemical is commonly used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It has the potential for applications in the development of drugs for the treatment of various diseases and conditions, as well as in the synthesis of other complex organic molecules. As with all chemicals, proper handling and safety precautions should be taken when working with 1-(3-Iodobenzyl)pyrrolidine to avoid any potential hazards.

InChI:InChI=1/C11H14IN/c12-11-5-3-4-10(8-11)9-13-6-1-2-7-13/h3-5,8H,1-2,6-7,9H2

Upstream product

• 57455-06-8 3-iodobenzylalcohol 
• 123-75-1 pyrrolidine 
• 696-41-3 m-iodobenzaldehyde 

Downstream Products

• 696-41-3 m-iodobenzaldehyde 
• 1138035-55-8 tert-butyl {[4-(2-fluorophenyl)-5-{[3-(pyrrolidin-1-ylmethyl)phenyl]thio}-1,3-thiazol-2-yl]methyl}methylcarbamate 

Relevant articles and documents

C8-substituted pyrido[3,4-d]pyrimidin-4(3H)-ones: Studies towards the identification of potent, cell penetrant Jumonji C domain containing histone lysine demethylase 4 subfamily (KDM4)inhibitors, compound profiling in cell-based target engagement assays

Residues in the histone substrate binding sites that differ between the KDM4 and KDM5 subfamilies were identified. Subsequently, a C8-substituted pyrido[3,4-d]pyrimidin-4(3H)-one series was designed to rationally exploit these residue differences between

5-Membered heterocyclic compound

The present invention provides 5-membered heterocycle compounds represented by the following general formula (I): The present compounds have a superior acid secretion inhibitory effect, and shows an antiulcer activity and the like.