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515604

Sigma-Aldrich

4-Iodobenzyl bromide

95%

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Synonym(s):
α-Bromo-4-iodotoluene, 1-(Bromomethyl)-4-iodobenzene, 4-(Bromomethyl)iodobenzene
Linear Formula:
IC6H4CH2Br
CAS Number:
Molecular Weight:
296.93
Beilstein/REAXYS Number:
2325160
MDL number:
PubChem Substance ID:
EC Index Number:
7000468
NACRES:
NA.22

Quality Level

assay

95%

mp

78-82 °C (lit.)

storage temp.

2-8°C

SMILES string

BrCc1ccc(I)cc1

InChI

1S/C7H6BrI/c8-5-6-1-3-7(9)4-2-6/h1-4H,5H2

InChI key

BQTRMYJYYNQQGK-UHFFFAOYSA-N

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This Item
209538681997760048
4-Iodobenzyl bromide 95%

515604

4-Iodobenzyl bromide

4-Fluorobenzyl bromide 97%

209538

4-Fluorobenzyl bromide

3,4-Dichlorobenzyl bromide 97%

681997

3,4-Dichlorobenzyl bromide

2-Chloro-4-methoxybenzyl bromide 97%

760048

2-Chloro-4-methoxybenzyl bromide

mp

78-82 °C (lit.)

mp

-

mp

-

mp

53-57 °C

storage temp.

2-8°C

storage temp.

-

storage temp.

-

storage temp.

−20°C

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible, corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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S De Bruyne et al.
Journal of labelled compounds & radiopharmaceuticals, 52(8), 304-311 (2009-09-12)
Dopamine transporter (DAT) neuroimaging is a useful tool in Parkinson's disease diagnosis, staging and follow-up providing information on the integrity of the dopaminergic neurotransmitter system in vivo. 4-(2-(Bis(4-fluorophenyl)-methoxy)ethyl)-1-(4-iodobenzyl)piperidine (7) has nanomolar affinity for DAT and better selectivity over the other
Guillermo E Negrón-Silva et al.
Molecules (Basel, Switzerland), 18(4), 4613-4627 (2013-04-20)
Ten 1,4-disubstituted 1,2,3-triazoles were synthesized from one of 1-(azido-methyl)benzene, 1-(azidomethyl)-4-fluorobenzene, 1-(azidomethyl)-4-chlorobenzene, 1-(azidomethyl)-4-bromobenzene or 1-(azidomethyl)-4-iodobenzene, generated in situ from sodium azide and the corresponding benzyl halide, and dipropargyl uracil or dipropargyl thymine. Optimal experimental conditions were established for the conventional click
M E Van Dort et al.
Bioorganic & medicinal chemistry letters, 11(8), 1045-1047 (2001-05-01)
A series of arylhydantoin derivatives modeled after the antiandrogen RU 58841 was generated to identify potential candidates for development as androgen receptor (AR) radioligands. Side-chain modified derivatives of RU 58841, suitable for labeling with either carbon-11 or radiohalogens (fluorine-18, iodine-123)
Yaws CL.
Thermophysical Properties of Chemicals and Hydrocarbons, 537-537 (2014)
Yaws CL.
The Yaws Handbook of Physical Properties for Hydrocarbons and Chemicals, 142-142 (2015)

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