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Iodobenzene

Iodobenzene

CAS: 591-50-4

Molecular Formula: C6H5I

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Iodobenzene - Names and Identifiers

Name Iodobenzene
Synonyms iodo-benzen
IODOBENZENE
Iodobenzene
iodinebenzol
Phenyliodide
Benzene,iodo-
Phenyl iodide
benzeneiodide
Benzene, iodo-
Benzene iodide
AKOS BBS-00004395
CAS 591-50-4
EINECS 209-719-6
InChI InChI=1/C6H6.HI/c1-2-4-6-5-3-1;/h1-6H;1H/p-1
InChIKey SNHMUERNLJLMHN-UHFFFAOYSA-N

Iodobenzene - Physico-chemical Properties

Molecular FormulaC6H5I
Molar Mass204.01
Density1.823 g/mL at 25 °C (lit.)
Melting Point-29 °C (lit.)
Boling Point188 °C (lit.)
Flash Point74 °C
Water Solubilityinsoluble
Solubility 0.34g/l (experimental)
AppearanceLiquid
Specific Gravity1.823
ColorClear yellow
Merck14,5029
BRN1446140
Storage ConditionStore below +30°C.
SensitiveLight Sensitive
Refractive Indexn20/D 1.62(lit.)
Physical and Chemical PropertiesDensity 1.82
melting point -29°C
boiling point 188°C
refractive index 1.618-1.62
flash point 74°C
water-soluble insoluble
UseFor Organic synthesis

Iodobenzene - Risk and Safety

Risk CodesR22 - Harmful if swallowed
R36 - Irritating to the eyes
R20/22 - Harmful by inhalation and if swallowed.
Safety DescriptionS26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36 - Wear suitable protective clothing.
S23 - Do not breathe vapour.
UN IDsNA 1993 / PGIII
WGK Germany3
RTECSDA3390000
FLUKA BRAND F CODES8
TSCAYes
HS Code29036990
Hazard NoteIrritant

Iodobenzene - Reference Information

NIST chemical information Information provided by: webbook.nist.gov (external link)
EPA chemical information Information provided by: ofmpub.epa.gov (external link)
Overview Iodobenzene (Iodobenzene), also known as iodobenzene, is an iodine substitute for benzene. The molecular formula is C6H5I, which is colorless and has a special odor. Liquid, insoluble in water, soluble in chloroform, ether and ethanol. Sensitive to light, the color of the light gradually turns yellow. Flash point 74 ℃. Since C- I bond energy is lower than C- Cl and C- Br bond energy, iodobenzene is more reactive than chlorobenzene and bromobenzene. It can react with magnesium to produce the Grignard reagent phenylmagnesium iodide (PhMgI), which can be used as a synthon equivalent of phenyl anions in organic synthesis. Iodobenzene can also be used as a raw material in the coupling reaction, Heck reaction and other metal-catalyzed coupling reactions.
Use Used as standard refractive index liquid
Used in organic synthesis or as refractive index standard liquid.
Used in organic synthesis, it is also a general reagent, which can be used as refractive index standard solution
production method is obtained by diazotization and replacement of aniline. Add 30% hydrochloric acid and aniline to water, stir and cool to 2 ℃, slowly add sodium nitrite solution dropwise, and control the temperature not to exceed 12 ℃. When dropping the last part of sodium nitrite solution, use potassium iodide starch test paper to test, and the blue color is the end point of the reaction to obtain the diazotized solution. Add the potassium iodide solution to the diazotization solution several times, release nitrogen at this time, and leave it for 2 hours until no nitrogen escapes. After cooling, the upper water solution is divided. Add 10% sodium hydroxide solution to make the reaction solution to pH14. Steam distillation is carried out, the distillate is divided into water layer, dried and fractionated at normal pressure, and the fraction at 184-188 ℃ is collected, which is iodobenzene with 77% yield.
toxic substance data information provided by: pubchem.ncbi.nlm.nih.gov (external link)
Last Update:2024-04-09 15:16:46
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View History
Iodobenzene
1H-Indole-5-carboxaldehyde, 1-ethyl-
TIANFU-CHEM 3-CHLORO-2-FLUORO-5-(TRIFLUOROMETHYL)PYRIDINE
784992-00-3
11092-32-3
851-49-0
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