Thiazolium, 2,3-dimethyl-4-phenyl-, iodide

Base Information

• Chemical Name: Thiazolium, 2,3-dimethyl-4-phenyl-, iodide
• CAS No.: 5968-24-1
• Molecular Formula: C11H12NS.I
• Molecular Weight: 317.193
• DSSTox Substance ID: DTXSID20483194
• Mol file: 5968-24-1.mol

Synonyms:Thiazolium, 2,3-dimethyl-4-phenyl-, iodide;5968-24-1;2,3-dimethyl-4-phenyl-1,3-thiazol-3-ium;iodide;DTXSID20483194;AKOS034450833;Z56756335

Chemical Property of Thiazolium, 2,3-dimethyl-4-phenyl-, iodide

Chemical Property:

• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 316.97352
• Heavy Atom Count: 14
• Complexity: 166

Purity/Quality:

95% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=[N+](C(=CS1)C2=CC=CC=C2)C.[I-]

Technology Process of Thiazolium, 2,3-dimethyl-4-phenyl-, iodide

There total 2 articles about Thiazolium, 2,3-dimethyl-4-phenyl-, 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:

2-methyl-4-phenylthiazole (1826-16-0) + methyl iodide (74-88-4) → 2,3-dimethyl-4-phenylthiazolium iodide (5968-24-1)

Guidance literature:

at 80 ℃; im Rohr;

Reference yield:

α-bromoacetophenone (70-11-1) → 2,3-dimethyl-4-phenylthiazolium iodide (5968-24-1)

Guidance literature:

Multi-step reaction with 2 steps

1: ethanol

In ethanol;

Reference yield: 32.0%

2,3-dimethyl-4-phenylthiazolium iodide (5968-24-1) + p-methylphenacyl chloride (4209-24-9) → 3,4-dimethyl-2-(4-methylbenzoyl)-5-phenyl-1,4-thiazine

Guidance literature:

With sodium hydroxide; In methanol; Ambient temperature;

upstream raw materials:

2-methyl-4-phenylthiazole

methyl iodide

α-bromoacetophenone

Downstream raw materials:

4-(N,N-dimethylamino)-N-(3-methyl-4-phenylthiazolio-2-methylidene) aniline iodide

1,3-bis-(3-methyl-4-phenyl-thiazol-2-yl)-trimethinium ; iodide

2-[4-(N-acetyl-anilino)-buta-1,3-dienyl]-3-methyl-4-phenyl-thiazolium; iodide

2-[6-(N-acetyl-anilino)-hexa-1,3,5-trienyl]-3-methyl-4-phenyl-thiazolium; iodide