Vinyl iodide

Base Information

• Chemical Name: Vinyl iodide
• CAS No.: 593-66-8
• Molecular Formula: C2H3 I
• Molecular Weight: 153.95
• Hs Code.: 29033990
• European Community (EC) Number: 209-801-1
• UNII: N4F8F0IJ60
• DSSTox Substance ID: DTXSID6060476
• Nikkaji Number: J6.768G
• Wikidata: Q27122542
• Metabolomics Workbench ID: 57697
• Mol file: 593-66-8.mol

Synonyms:vinyl iodide

Chemical Property of Vinyl iodide

Chemical Property:

• Vapor Pressure: 244mmHg at 25°C
• Refractive Index: 1.5385
• Boiling Point: 56°Cat760mmHg
• Flash Point: 6.2°C
• PSA: 0.00000
• Density: 2.039g/cm³
• LogP: 1.56490
• Sensitive.: Light Sensitive
• Water Solubility.: Not miscible or difficult to mix in water.
• XLogP3: 1.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 0
• Exact Mass: 153.92795
• Heavy Atom Count: 3
• Complexity: 10.3

Purity/Quality:

99% ^*data from raw suppliers

Vinyl iodide ^*data from reagent suppliers

Safty Information:

• Pictogram(s): T
• Hazard Codes: T
• Statements: 23/24/25-45-22
• Safety Statements: 45-53-36-20

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C=CI
• Uses: Vinyl iodide is an important intermediate used in organic synthesis, chemical research and pharmaceuticals.

Technology Process of Vinyl iodide

There total 21 articles about Vinyl 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: 100.0%

→ vinyliodide (593-66-8)

Guidance literature:

Reference yield: 96.0%

Na2 S2 O3 + 1-chloro-2-iodoethane (624-70-4) + trans-1-isopropylsulfonyl-2-amino-6-(1-[3-fluorophenyl]-2-(bromo)ethen-1-yl)benzimidazole (186093-26-5) → trans-1-Isopropylsulfonyl-2-Amino-6-(1-[3-Fluorophenyl]-2-(Iodo)ethen-1-yl)benzimidazole + vinyliodide (593-66-8)

Guidance literature:

With tert.-butyl lithium; phenyllithium; In tetrahydrofuran; cyclohexane; ethyl acetate; pentane;

Reference yield: 78.0%

→ vinyliodide (593-66-8) + (E)-3,7-dimethyloct-3-enol (56134-54-4)

Guidance literature:

upstream raw materials:

1,1-diiodoethane

1,2-Diiodoethane

acetylene

methylene

Downstream raw materials:

1,1-diiodoethane

1,1,2-tribromoethane

1,2-dimethyl cyclohex-2-ene-1,2-dicarboxylate

(1S,2R)-Cyclohex-3-ene-1,2-dicarboxylic acid dimethyl ester

Refernces

• 1、 -. "Synthesis of epothilones, intermediates thereto and analogues thereof". . . Retrieved 2008/06/13.
• 2、 -. "Epothilone derivatives and methods for making and using the same". . . Retrieved 2008/06/13.