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515604

Sigma-Aldrich

4-Iodobenzyl bromide

95%

Synonym(s):

α-Bromo-4-iodotoluene, 1-(Bromomethyl)-4-iodobenzene, 4-(Bromomethyl)iodobenzene

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About This Item

Linear Formula:
IC6H4CH2Br
CAS Number:
16004-15-2
Molecular Weight:
296.93
Beilstein:
2325160
MDL number:
MFCD00209656
UNSPSC Code:
12352100
PubChem Substance ID:
24873836
EC Index Number:
7000468
NACRES:
NA.22

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

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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
Yaws CL.
The Yaws Handbook of Physical Properties for Hydrocarbons and Chemicals, 142-142 (2015)
Yaws CL.
Thermophysical Properties of Chemicals and Hydrocarbons, 537-537 (2014)
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)
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