4-Iodobenzyl bromide
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4-Iodobenzyl bromide
structure -
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CAS No:
16004-15-2
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Formula:
C7H6BrI
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Chemical Name:
4-Iodobenzyl bromide
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Synonyms:
Benzene,1-(bromomethyl)-4-iodo-;Toluene,α-bromo-p-iodo-;1-(Bromomethyl)-4-iodobenzene;p-Iodobenzyl bromide;4-Iodobenzyl bromide;α-Bromo-p-iodotoluene
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CAS No:
Characteristics
0
4
Light yellow Adhering Crystalline Powder
2.0672 (rough estimate)
84.5-85.0 °C
200-205 °C @ Press: 4 Torr
140°C/15mm
1.6500 (estimate)
Insoluble in water.
2-8°C
0.0202mmHg at 25°C
Safety Information
Ⅱ
8
UN 3261 8/PG 2
3
34-63-42/43-36/37/38
26-36/37/39-45-23
C,T
Corrosive/Lachrymatory/Light Sensitive
P280-P305 + P351 + P338-P310
H314
|Danger|H314 (99.28%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]|P260, P264, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P363, P405, and P501|Aggregated GHS information provided by 140 companies from 8 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
4-Iodobenzyl bromide Use and Manufacturing
Synthesis of Compound 1D [0026] p-Iodotoluene (Compound 1C, 25 g), N-bromosuccinimide (23.5 g) and benzoyl peroxide (375 mg) were added to carbon tetrachloride (375 ml) and refluxed with heating for 7 hours under photoirradiation. Further, the reaction mixture was stirred overnight at room temperature, then insoluble matters were removed by filtration, and the filtrate was concentrated under reduced pressure. The concentrated residue was recrystallized from ethyl acetate and hexane to obtain Compound 1D (yield: 60.3percent). [0027] NMR chemical shift, CDCl3, TMS as standard [0028] d 7.72 (d, 2H), 7.14 (d, 2H), 4.39 (s, 2H)Step 1
Computed Properties
Molecular Weight:296.93
XLogP3:4
Rotatable Bond Count:1
Exact Mass:295.86976
Monoisotopic Mass:295.86976
Heavy Atom Count:9
Complexity:77
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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