| Identification | More | [Name]
4-Iodobenzyl bromide | [CAS]
16004-15-2 | [Synonyms]
1-BROMOMETHYL-4-IODO-BENZENE
4-IODOBENZYL BROMIDE
ALPHA-BROMO-4-IODOTOLUENE
P-IODOBENZYL BROMIDE
4-Iodobenzyl Bromide p-Iodobenzyl Bromide
à-bromo-4-iodotoluene
4-Iodobenzyl bromide 97%
p-odobenzyl bromide | [Molecular Formula]
C7H6BrI | [MDL Number]
MFCD00209656 | [Molecular Weight]
296.93 | [MOL File]
16004-15-2.mol |
| Chemical Properties | Back Directory | [Appearance]
light yellow adhering crystalline powder | [Melting point ]
78-82 °C(lit.)
| [Boiling point ]
140°C 15mm | [density ]
2.0672 (rough estimate) | [refractive index ]
1.6500 (estimate) | [Fp ]
140°C/15mm | [storage temp. ]
2-8°C
| [form ]
Adhering Crystalline Powder | [color ]
Light yellow | [Water Solubility ]
Insoluble in water. | [Sensitive ]
Light Sensitive/Lachrymatory | [BRN ]
2325160 | [InChI]
InChI=1S/C7H6BrI/c8-5-6-1-3-7(9)4-2-6/h1-4H,5H2 | [InChIKey]
BQTRMYJYYNQQGK-UHFFFAOYSA-N | [SMILES]
C1(CBr)=CC=C(I)C=C1 | [CAS DataBase Reference]
16004-15-2(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
C,T | [Risk Statements ]
R34:Causes burns.
R63:Possible risk of harm to the unborn child.
R42/43:May cause sensitization by inhalation and skin contact .
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S23:Do not breathe gas/fumes/vapor/spray (appropriate wording to be specified by the manufacturer) . | [RIDADR ]
UN 3261 8/PG 2
| [WGK Germany ]
3
| [Hazard Note ]
Corrosive/Lachrymatory/Light Sensitive | [HazardClass ]
8 | [HazardClass ]
IRRITANT | [PackingGroup ]
Ⅱ | [HS Code ]
29039990 |
| Hazard Information | Back Directory | [Chemical Properties]
light yellow adhering crystalline powder | [Uses]
4-Iodobenzyl bromide is used as an organic chemical synthesis intermediate. |
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