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515604

4-Iodobenzyl bromide

Name: 4-Iodobenzyl bromide
Brand: ALDRICH

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

NACRES:

NA.22

EC Index Number:

7000468

PubChem Substance ID:

24873836

UNSPSC Code:

12352100

MDL number:

MFCD00209656

Beilstein/REAXYS Number:

2325160

Assay:

95%

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Properties

Quality Level

100

assay

95%

mp

78-82 °C (lit.)

functional group

bromo, iodo

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

Description

pictograms

GHS05

signalword

Danger

hcodes

H314

pcodes

P260 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

Regulatory Information

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Synthesis, radiosynthesis and in vivo evaluation of [I]-4-(2-(bis(4-fluorophenyl)methoxy)ethyl)-1-(4-iodobenzyl)piperidine as a selective tracer for imaging the dopamine transporter.

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

Synthesis of new 1,2,3-triazole derivatives of uracil and thymine with potential inhibitory activity against acidic corrosion of steels.

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)

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Global Trade Item Number

SKU	GTIN
515604-1G	04061826003084
515604-5G	04061832500133