Name | 1-Iodonaphthalene |
Synonyms | Iodonaphthalene iodonaphthalene 1-Iodonaphthalene 1-IODONAPHTHALENE 1-iodo-naphthalen 1-NAPHTHYL IODIDE 1-naphthyl iodide naphthalene,1-iodo- naphthalene, 1-iodo- Naphthalene, 1-iodo- alpha-iodonaphthalene alpha-Iodonaphthalene |
CAS | 90-14-2 |
EINECS | 201-968-9 |
InChI | InChI=1/C10H7I/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H |
InChIKey | NHPPIJMARIVBGU-UHFFFAOYSA-N |
Molecular Formula | C10H7I |
Molar Mass | 254.07 |
Density | 1.74 g/mL at 25 °C (lit.) |
Melting Point | 4°C |
Boling Point | 163-165 °C/15 mmHg (lit.) |
Flash Point | >230°F |
Water Solubility | Slightly soluble in water. |
Solubility | 0.007g/l |
Vapor Presure | 0.00182mmHg at 25°C |
Appearance | liquid (clear) |
Specific Gravity | 1.74 |
Color | clear very deep brown-yellow |
BRN | 1906415 |
Storage Condition | Keep in dark place,Inert atmosphere,Room temperature |
Sensitive | Light Sensitive |
Refractive Index | n20/D 1.701(lit.) |
Physical and Chemical Properties | Melting Point: 4°C Boiling Point: 163-165°C 15mm Hg(lit.) density: 1.74g/mL at 25°C(lit.) refractive index: n20/D 1.701(lit.) flash point: >230 °F form: liquid (clear) color: clear very deep brown-yellow appearance: yellow to brown transparent liquid |
Use | For Organic synthesis |
Hazard Symbols | Xi - Irritant |
Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. S37/39 - Wear suitable gloves and eye/face protection |
WGK Germany | 3 |
FLUKA BRAND F CODES | 8 |
TSCA | Yes |
HS Code | 29036990 |
NIST chemical information | information provided by: webbook.nist.gov (external link) |
EPA chemical substance information | information provided by: ofmpeb.epa.gov (external link) |
Introduction | 1-iodonaphthalene is an organic compound with the chemical formula C10H7I. It can be prepared from 1-bromonaphthalene and sodium iodide in dioxane reaction, or by naphthalene and N-iodosuccinimide in 1,1,1,3,3, the reaction in 3-hexafluoro-2-propanol results in the formation of small amounts of 2-iodo-byproducts. |
Application | 1-iodonaphthalene can be used in organic synthesis, which is coupled with Phenylboronic acid in the presence of potassium phosphate and catalyst, 1-phenylnaphthalene can be obtained. It reacts with potassium cyanide and the iodine is substituted with a cyano group to give 1-naphthonitrile. |
Use | for organic synthesis |