All Photos(3)
Synonym(s):
α-Bromo-4-iodotoluene, 1-(Bromomethyl)-4-iodobenzene, 4-(Bromomethyl)iodobenzene
Linear Formula:
IC6H4CH2Br
CAS Number:
Molecular Weight:
296.93
Beilstein:
2325160
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
EC Index Number:
7000468
NACRES:
NA.22
Recommended Products
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
Related Categories
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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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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