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2,5-Diiodothiophene

CAS No.:
625-88-7
Catalog Number:
AG003FYP
Molecular Formula:
C4H2I2S
Molecular Weight:
335.9326
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Product Description
Catalog Number:
AG003FYP
Chemical Name:
2,5-Diiodothiophene
CAS Number:
625-88-7
Molecular Formula:
C4H2I2S
Molecular Weight:
335.9326
MDL Number:
MFCD00014525
IUPAC Name:
2,5-diiodothiophene
InChI:
InChI=1S/C4H2I2S/c5-3-1-2-4(6)7-3/h1-2H
InChI Key:
PNYWRAHWEIOAGK-UHFFFAOYSA-N
SMILES:
Ic1ccc(s1)I
EC Number:
210-915-9
NSC Number:
80411
Properties
Complexity:
58.7  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
335.797g/mol
Formal Charge:
0
Heavy Atom Count:
7  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
335.929g/mol
Monoisotopic Mass:
335.797g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
28.2A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3  
Literature
Title Journal
Organic-skinned inorganic nanoparticles: surface-confined polymerization of 6-(3-thienyl)hexanoic acid bound to nanocrystalline TiO2. Nanoscale research letters 20110101
Improved hybrid solar cells via in situ UV polymerization. Small (Weinheim an der Bergstrasse, Germany) 20090803
Resonance Raman study of the A-band short-time photodissociation dynamics of 2,5-di-iodothiophene. The Journal of chemical physics 20081207
Ring opening of 2,5-didehydrothiophene: matrix photochemistry of C4H2S isomers. The Journal of organic chemistry 20061222
Dendritic aggregation of oligothiophene during desorption of 2,5-diiodothiophene multilayer and topography-induced alignment of oligothiophene nanofibers. The journal of physical chemistry. B 20061019
Physical insights into the photoactivated Ullmann coupling process producing highly conjugated oligothiophene films on a copper substrate. The journal of physical chemistry. B 20060420
Maskless fabrication of polythiophene patterns by photochemical conversion of regioselectively condensed 2,5-diiodothiophene. Langmuir : the ACS journal of surfaces and colloids 20050719
Prediction of genotoxicity of chemical compounds by statistical learning methods. Chemical research in toxicology 20050601
Ethynyl pi-extended 2,5-diphenyl-1,3,4-oxadiazoles and 2-phenyl 5-(2-thienyl)-1,3,4-oxadiazoles: synthesis, X-ray crystal structures and optical properties. Organic & biomolecular chemistry 20041121
Properties