189100-30-9

Basic information

• Product Name: Benzonitrile, 4-(3-pyridinylamino)-
• CAS NO: 189100-30-9
• Molecular Formula: C12H9N3
• Molecular Weight: 195.224
• Mol File: 189100-30-9.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Benzonitrile, 4-(3-pyridinylamino)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzonitrile, 4-(3-pyridinylamino)-(189100-30-9)
• EPA Substance Registry System: Benzonitrile, 4-(3-pyridinylamino)-(189100-30-9)

Safety Data

• Hazardous Substances Data: 189100-30-9(Hazardous Substances Data)

Upstream product

• 1016872-53-9 C₁₄H₁₁N₃O₂ 
• 462-08-8 pyridin-3-ylamine 
• 695-37-4 3-fluoropyridine-1-oxide 
• 623-03-0 4-Cyanochlorobenzene 
• 623-00-7 4-bromobenzenecarbonitrile 
• 189100-17-2 3-(4-cyanophenyl)aminopyridine N-oxide 
• 126747-14-6 4-cyanophenylboronic acid 

Downstream Products

• 1268526-18-6 C₂₃H₂₉N₃ 
• 1310693-60-7 5-(5-cyclohexylpentyl)-5H-pyrido[3,2-b]indol-8-carbonitrile 
• 1310693-38-9 8-cyano-5-(5-cyclohexylpentyl)-1-methyl-5H-pyrido[3,2-b]indol-1-ium iodide 

Relevant articles and documents

A Tetraarylpyrrole-Based Phosphine Ligand for the Palladium-Catalyzed Amination of Aryl Chlorides

A tetraarylpyrrole-based phosphine ligand L1 in combination with Pd(dba)2 provided a catalyst for the Buchwald-Hartwig amination reaction. A variety of amines were rapidly coupled with aryl chlorides at a Pd loading of 0.5 mol%. The selective monoarylation of aliphatic primary amines was achieved in the presence of 0.8 equiv. water. Comparison experiments were also conducted, which revealed that the catalytic activity of L1 is superior to representative phosphine ligands in the Pd-catalyzed C?N coupling of various amines. (Figure presented.).

PHOSPHINE COMPOUND, CROSSLINKED COMPOSITION, AND MANUFACTURING METHOD OF AROMATIC AMINE COMPOUND

PROBLEM TO BE SOLVED: To provide a phosphine compound capable of constituting a transition metal complex excellent in reaction speed and selectivity as a catalyst. SOLUTION: There is provided a phosphine compound represented by the formula (I). In the formula Ar represents each independently an aryl group which may be substituted, R1 represents each independently a linear, branched or cyclic alkyl group, R2 represents each independently a linear, branched or cyclic alkyl group, alkoxy group or aryl group which may be substituted, or neighboring 2 R2 are bound each other to form a ring, and n represents an integer of 0 to 4. SELECTED DRAWING: None COPYRIGHT: (C)2020,JPOandINPIT

δ-carbolines and their ring-opened analogs: Synthesis and evaluation against fungal and bacterial opportunistic pathogens

Previous studies have indicated that the δ-carboline (2) ring system derived from the natural product cryptolepine (1) may represent a pharmacophore for anti-infective activity. This paper describes the design and synthesis of a small library of substitut