(Z)-(benzylsulfanyl)(1-methylpyridin-2(1H)-ylidene)-N-oxomethanaminium iodide

Base Information

• Chemical Name: (Z)-(benzylsulfanyl)(1-methylpyridin-2(1H)-ylidene)-N-oxomethanaminium iodide
• CAS No.: 107535-23-9
• Molecular Formula: C₁₄H₁₅N₂OS*I
• Molecular Weight: 386.256
• Mol file: 107535-23-9.mol

Synonyms:Pyridinium,2-[(hydroxyimino)[(phenylmethyl)thio]methyl]-1-methyl-, iodide (9CI); RA 49

Chemical Property of (Z)-(benzylsulfanyl)(1-methylpyridin-2(1H)-ylidene)-N-oxomethanaminium iodide

Chemical Property:

• Vapor Pressure: 5.29E-05mmHg at 25°C
• Boiling Point: 347.7°Cat760mmHg
• Flash Point: 164.1°C
• Density: g/cm³

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of (Z)-(benzylsulfanyl)(1-methylpyridin-2(1H)-ylidene)-N-oxomethanaminium iodide

There total 3 articles about (Z)-(benzylsulfanyl)(1-methylpyridin-2(1H)-ylidene)-N-oxomethanaminium iodide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 72.0%

benzyl-2-pyridylhydroxyiminomethyl thioether (107535-16-0) + methyl iodide (74-88-4) → benzyl-2-pyridylhydroxyiminomethylthioether methiodide (107535-23-9)

Guidance literature:

In acetone; for 96h; Ambient temperature;

Reference yield:

sodium benzylmercaptide (3492-64-6) → benzyl-2-pyridylhydroxyiminomethylthioether methiodide (107535-23-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 64 percent / methanol / 0.5 h

2: 72 percent / acetone / 96 h / Ambient temperature

In methanol; acetone;

Reference yield:

2-pyridylhydroxyiminomethyl chloride (69716-28-5) → benzyl-2-pyridylhydroxyiminomethylthioether methiodide (107535-23-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 64 percent / methanol / 0.5 h

2: 72 percent / acetone / 96 h / Ambient temperature

In methanol; acetone;

upstream raw materials:

benzyl-2-pyridylhydroxyiminomethyl thioether

methyl iodide

sodium benzylmercaptide

2-pyridylhydroxyiminomethyl chloride