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

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

Uses

Used in Pharmaceutical Industry:
1-(3-IODOBENZYL)PYRROLIDINE is used as an intermediate in organic synthesis for the production of pharmaceuticals. Its unique structure allows for the development of drugs targeting a range of diseases and conditions, making it a valuable component in the creation of novel therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(3-IODOBENZYL)PYRROLIDINE is utilized as an intermediate in the synthesis of various agrochemicals. Its role in the development of these chemicals aids in enhancing agricultural productivity and protecting crops from pests and diseases.
Used in Organic Synthesis:
1-(3-IODOBENZYL)PYRROLIDINE is also used as a building block in the synthesis of other complex organic molecules. Its presence in these molecules can lead to the creation of new compounds with diverse applications, further expanding the utility of this chemical compound.

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

THIAZOLE AND OXAZOLE KINASE INHIBITORS

The present invention is concerned with substituted azole derivatives that selectively modulate, regulate, and/or inhibit signal transduction mediated by certain native and/or mutant proteine kinases implicated in a variety of human and animal diseases such as cell proliferative, metabolic, allergic, and degenerative disorders. In particular, several of these compounds are potent and selective Flt-3 inhibitors or/and syk inhibitors.

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.