166830-87-1

Usage

Organotellurium compound

Contains a phenyltelluro group attached to a propanamine molecule

Use

Commonly used as a reagent in organic synthesis and catalysis

Application

Potential applications in the field of medicinal chemistry, specifically in the development of novel drugs and pharmaceuticals

Unique properties

Exhibits unique chemical properties and reactivity due to the presence of the tellurium atom, making it a valuable tool in various chemical and biological processes.

Upstream product

• 32294-60-3 diphenyl ditelluride 
• 6276-54-6 3-chloropropylamine hydrochloride 

Downstream Products

• 18421-49-3 trans-Pt(phenyl)Cl(triphenylphosphine)2 
• 1187664-51-2 N-(3-(phenyltellanyl)propyl)formamide 
• 1202354-00-4 4,4'-(3,6-dimethyl-1,4-benzoquinone-2,5-diyl)bis(N-(3-(phenyltelluryl)propyl)butanamide) 
• 1202354-02-6 6-(1,4-naphthoquinone-2-ylamino)-N-(3-(phenyltelluryl)propyl)hexanamide 
• 1202353-97-6 4-(3-methyl-1,4-naphthoquinone-2-yl)-N-(3-(phenyltelluryl)propyl)butanamide 
• 1187664-47-6 (3-isocyanopropyl)(phenyl)tellane 
• 1612261-05-8 (E)-(3-(phenyltellanyl)propylcarbamoyl)methyl cinnamate 
• 1612261-04-7 (E)-N-((3-(phenyltellanyl)propylcarbamoyl)methyl)-N-(4-methoxyphenyl)cinnamamide 
• 1612261-01-4 N-((3-(phenyltellanyl)propylcarbamoyl)methyl)-N-(4-methoxyphenyl)benzamide 
• 1612260-98-6 tert-butyl [(((3-(phenyltellanyl)propylcarbamoyl)methoxy)carbonyl)methyl]carbamate 
• 1612260-97-5 C₂₅H₃₃N₃O₅Te 
• 1261216-11-8 2,6-bis({N-[3-(phenyltelluro)propyl]}benzimidoyl)-4-methylphenol 
• 166830-88-2 [PtCl₂*3-aminopropyl(phenyl)telluride] 
• 166830-91-7 [PdCl₂*3-aminopropyl(phenyl)telluride] 

Relevant academic research and scientific papers

En Route Activity of Hydration Water Allied with Uranyl (UO22+) Salts Amid Complexation Reactions with an Organothio-Based (O, N, S) Donor Base

This study provides en route activity of hydration water allied with uranyl salts amid complexation reactions with a donor species L bearing O, N, and S (phenolic, -OH; imine, -HC=N-; and thio-, -S-) donor functionalities. The UO22+/

Terminal organylchalcogenoethyl- and -propylamines and their Schiff base derivatives

A series of organoselanyl- and organotellanyl-substituted ethyl- and propylamines and their hydrochlorides, as well as 2-(methylsulfanyl)ethylamine have been synthesized. Efficient general synthetic routes have been developed to chalcogen(S, Se, Te)-conta

Synthesis and multinuclear NMR studies of 3-aminopropyl(aryl)chalcogenides, NH2CH2CH2CH2EAr (E=Se, Te), and their complexes with Pt(II) and Pd(II)

The asymmetric ligands, 3-aminopropyl(aryl)tellurides (1a, 1b) and 3-aminopropyl(phenyl)selenide (2) and their complexes with platinum(II) and palladium(II), viz. (3, 4), (5), (6, 7), (8), (9) and (10) have been made and characterized.Complexes 3-8, have square planar geometry around the metal (Pd or Pt) with the (Te,N)- or (Se,N)-ligand coordinated in a bidentate mode and the two chlorines cis to each other.Complex 9 also has a square planar geometry, with Me trans to nitrogen and Cl trans to tellurium.In complex 10 where Pd appears to be in a square planar geometry the two tellurium atoms are judged to be trans to each other.Keywords: Alkyl; Amine; Aryl; Group 16; Group 10; Chalcogenide