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About This Item
Linear Formula:
ClC6H3(I)CH3
CAS Number:
Molecular Weight:
252.48
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
assay
98%
refractive index
n20/D 1.624 (lit.)
bp
239 °C (lit.)
density
1.81 g/mL at 25 °C (lit.)
SMILES string
Cc1cc(I)ccc1Cl
InChI
1S/C7H6ClI/c1-5-4-6(9)2-3-7(5)8/h2-4H,1H3
InChI key
MMBDKGFWRIYSRD-UHFFFAOYSA-N
General description
2-Chloro-5-iodotoluene is a halogenated hydrocarbon.
Application
2-Chloro-5-iodotoluene may be used to synthesize:
- 1-(4-chloro-3-methylphenyl)-1H-pyrrolo[2,3-c]pyridine
- bromomethyl-2-chloro-5-iodobenzene
- 3-(4′-chloro-3′-tolyl)thiophene
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Frédéric Stauffer et al.
Bioorganic & medicinal chemistry letters, 22(5), 1860-1863 (2012-02-18)
Aromatase inhibition is the new standard of care for estrogen receptor positive breast cancer and has also potential for treatment of other diseases such as endometriosis. Simple and readily available 3-pyridyl arylethers and 1-aryl pyrrolo[2,3-c]pyridines recapitulating the key pharmacophore elements
Synthesis and characterization of all-conjugated graft copolymers comprised of n-type or p-type backbones and poly (3-hexylthiophene) side chains.
Wang J, et al.
Macromolecules, 46(5), 1783-1793 (2013)
Susanna Tchilibon et al.
Journal of medicinal chemistry, 48(6), 1745-1758 (2005-03-18)
A series of ring-constrained (N)-methanocarba-5'-uronamide 2,N(6)-disubstituted adenine nucleosides have been synthesized via Mitsunobu condensation of the nucleobase precursor with a pseudosugar ring containing a 5'-ester functionality. Following appropriate functionalization of the adenine ring, the ester group was converted to the
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