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3437-95-4 | 2-Iodothiophene
CAS No: 3437-95-4 Catalog No: AG0033D9 MDL No:MFCD00005424
Product Description
Catalog Number:
AG0033D9
Chemical Name:
2-Iodothiophene
CAS Number:
3437-95-4
Molecular Formula:
C4H3IS
Molecular Weight:
210.0361
MDL Number:
MFCD00005424
IUPAC Name:
2-iodothiophene
InChI:
InChI=1S/C4H3IS/c5-4-2-1-3-6-4/h1-3H
InChI Key:
ROIMNSWDOJCBFR-UHFFFAOYSA-N
SMILES:
Ic1cccs1
EC Number:
222-342-1
NSC Number:
1082
Properties
Complexity:
46.8
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
209.9g/mol
Formal Charge:
0
Heavy Atom Count:
6
Hydrogen Bond Acceptor Count:
1
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
210.032g/mol
Monoisotopic Mass:
209.9g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
28.2A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.6
Literature
| Title | Journal |
|---|---|
| Synthesis of redox-active, intramolecular charge-transfer chromophores by the [2+2] cycloaddition of ethynylated 2H-cyclohepta[b]furan-2-ones with tetracyanoethylene. | Chemistry (Weinheim an der Bergstrasse, Germany) 20110426 |
| Bis(2-thien-yl)acetyl-ene. | Acta crystallographica. Section E, Structure reports online 20091001 |
| Resonance Raman study of the A-band short-time photodissociation dynamics of 2,5-di-iodothiophene. | The Journal of chemical physics 20081207 |
| 9-(2-Thien-yl)-9H-carbazole. | Acta crystallographica. Section E, Structure reports online 20081201 |
| Functionalization through lithiation of (S)-N-(1-phenylpropyl)-2-phenylquinoline-4-carboxamide. Application to the labeling with carbon-11 of NK-3 receptor antagonist SB 222200. | The Journal of organic chemistry 20070316 |
| Facile synthesis of substituted thiophenes via Pd/C-mediated sonogashira coupling in water. | Bioorganic & medicinal chemistry letters 20061215 |
| Resonance Raman study of the A-band short-time photodissociation dynamics of 2-iodothiophene. | The Journal of chemical physics 20060807 |
| Stereospecific preparation of (Z)- and (E)-2,3-difluoro-3-stannylacrylic ester synthons and a new, efficient stereospecific route to (Z)- and (E)-2,3-difluoroacrylic esters. | The Journal of organic chemistry 20051223 |
| Prediction of genotoxicity of chemical compounds by statistical learning methods. | Chemical research in toxicology 20050601 |
| Fluoride-promoted cross-coupling reactions of alkenylsilanols. Elucidation of the mechanism through spectroscopic and kinetic analysis. | Journal of the American Chemical Society 20040421 |
| Cross-coupling reactions of alkenylsilanolates. Investigation of the mechanism and identification of key intermediates through kinetic analysis. | Journal of the American Chemical Society 20040421 |
| Palladium-catalyzed three-component assembling of allenes, organic halides, and arylboronic acids. | The Journal of organic chemistry 20020111 |
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