3437-95-4 | 2-Iodothiophene

Packsize	Purity	Availability	Price	Discounted Price
5g	98% (stabilized with Copper chip)	in stock	$6.00	$4.00
10g	98% (stabilized with Copper chip)	in stock	$9.00	$6.00
25g	98% (stabilized with Copper chip)	in stock	$18.00	$13.00
100g	98% (stabilized with Copper chip)	in stock	$52.00	$36.00
500g	98% (stabilized with Copper chip)	in stock	$255.00	$179.00

Description

• Catalog Number: AB44133
• Chemical Name: 2-Iodothiophene
• CAS Number: 3437-95-4
• Molecular Formula: C4H3IS
• Molecular Weight: 210.0361
• MDL Number: MFCD00005424
• SMILES: Ic1cccs1
• NSC Number: 1082

Computed Properties

• Complexity: 46.8
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 6
• Hydrogen Bond Acceptor Count: 1
• XLogP3: 2.6

Literature

• 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