2-Iodopropene

Base Information

• Chemical Name: 2-Iodopropene
• CAS No.: 4375-96-6
• Molecular Formula: C3H5 I
• Molecular Weight: 167.977
• Hs Code.: 2903399090
• European Community (EC) Number: 224-475-0
• UNII: Q4APE2VA7L
• DSSTox Substance ID: DTXSID00195925
• Nikkaji Number: J151.480F
• Wikidata: Q83068998
• Mol file: 4375-96-6.mol

Synonyms:2-Iodopropene;4375-96-6;2-iodo-1-propene;2-iodoprop-1-ene;Propene, 2-iodo-;1-Propene, 2-iodo-;Q4APE2VA7L;EINECS 224-475-0;2-iodo-prop-1-ene;Ethyl4-bromophenylacetate;UNII-Q4APE2VA7L;SCHEMBL171568;DTXSID00195925;AKOS006272052;FT-0612652

Chemical Property of 2-Iodopropene

Chemical Property:

• Vapor Pressure: 78.4mmHg at 25°C
• Melting Point: -99.29°C (estimate)
• Refractive Index: 1.5200
• Boiling Point: 85.2°C at 760 mmHg
• Flash Point: 18.1°C
• PSA: 0.00000
• Density: 1.83g/cm³
• LogP: 1.95500
• XLogP3: 2.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 0
• Exact Mass: 167.94360
• Heavy Atom Count: 4
• Complexity: 30.3

Purity/Quality:

98%Min ^*data from raw suppliers

2-IODOPROPENE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CC(=C)I

Technology Process of 2-Iodopropene

There total 3 articles about 2-Iodopropene 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: 40.0%

prop-1-yne (74-99-7) → 2-iodopropene (4375-96-6)

Guidance literature:

With hydrogen iodide; mercury iodide; at -30 ℃; for 3h;

Reference yield:

2,2-diiodopropane (630-13-7) → 2-iodopropene (4375-96-6)

Guidance literature:

With potassium carbonate;

Reference yield:

→ 2-iodopropene (4375-96-6)

Guidance literature:

Methylacetylen, J2;

DOI:10.1039/tf9716702085

upstream raw materials:

2,2-diiodopropane

prop-1-yne

Downstream raw materials:

7-(2,5-dimethoxyphenyl)-2-methylhept-1-en-6-yn-3-ol

2-methyl-1-hexen-3-yne

(5-methylhex-5-en-3-ynyloxymethyl)benzene

1-Isopropenyl-1-cyclohexanol

Refernces

• 1、 Griesbaum et al.. "". . p. 3151,3152-3154. Retrieved 1965.
• 2、 Bobrovnikov, M. N.,Turbanova, E. S.,Petrov, A. A.. "SYNTHESIS OF TRIFLUOROMETHYL- AND PENTAFLUOROPHENYLALKENYNES". . p. 1445 - 1449. Retrieved 2007/10/02.