| Weight | 169.993 g/mol |
|---|---|
| Formula | C3H7I |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
2-IODOPROPANE (75-30-9)
isopropyl iodide
Score:
#2221 in Physics
,
#2785 in Biochemistry
,
#6859 in Chemistry
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LabBot
- Catalytic reduction of Iodoethane and 2-Iodopropane at Carbon Electrodes Coated with Anodically Polymerized Films of Nickel(II) Salen (Analytical Chemistry, 1994)
- A mechanistic study of the photochemically initiated oxidative addition of isopropyl iodide to dimethyl(1,10-phenanthroline)platinum(II) (Journal of the American Chemical Society, 1985)
- Reactions of iodoethane, iodopropane, 2-iodopropane, chloroiodomethane adsorbed on silver(111) (The Journal of Physical Chemistry, 1991)
- Substituent effects on gas-phase photodissociation dynamics: Resonance Raman spectra of ethyl iodide, isopropyl iodide, and tert-butyl iodide (The Journal of Physical Chemistry, 1991)
- REACTION OF 4-FORMYL-1-METHYL PYRIDINIUM IODIDE OXIME (4-PAM) WITH ISOPROPYL METHYLPHOSPHONOFLUORIDATE, GB. (Biochemistry, 1965)
- Synthesis of DL-[3-11C]valine using [2-11C]isopropyl iodide, and preparation of L-[3-11C]valine by treatment with D-amino acid oxidase (International Journal of Radiation Applications and Instrumentation. Part A. Applied Radiation and Isotopes, 1987)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - isopropyl iodide
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SMILESCC(C)I
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InChIKeyFMKOJHQHASLBPH-UHFFFAOYSA-N
- Pubchem - 2-IODOPROPANE
- Wikipedia - isopropyl iodide
Isopropyl iodide is the organoiodine compound with the formula (CH3)2CHI. It is colorless, flammable, and volatile. Organic iodides are light-sensitive and take on a yellow colour upon storage, owing to the formation of iodine.
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2-IODOPROPANE
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