Molecular structure of 1,4-Phenylene diisocyanide, CAS Number: 935-16-0
1,4-Phenylene diisocyanide (CAS 935-16-0)
Alternate Names:
1,4-Diisocyanobenzene; 4-Isocyanophenylisocyanide
CAS Number:
935-16-0
Molecular Weight:
128.13
Molecular Formula:
C8H4N2
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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1,4-Phenylene diisocyanide belongs to the family of diisocyanide compounds and consists of a phenylene (benzene) ring with two isocyanide (-NC) functional groups attached at the 1 and 4 positions. It is a versatile building block used in organic synthesis and coordination chemistry. For example, 1,4-Diisocyanobenzene is used in the synthesis of the anti-tumor drug, imatinib mesylate. 1,4-Phenylene diisocyanide is known for its ability to form stable complexes with transition metals, making it valuable in the preparation of metal-organic frameworks (MOFs), coordination polymers, and other supramolecular assemblies.
1,4-Phenylene diisocyanide (CAS 935-16-0) References
- Low temperature conductance measurements of self-assembled monolayers of 1,4-phenylene diisocyanide. | Dupraz, CJ., et al. 2003. Chemphyschem. 4: 1247-52. PMID: 14653008
- Self-assembly of 1,4-phenylene diisocyanide and terephthalic acid on Ni, Cu and Pt. | Pranger, L. and Tannenbaum, R. 2005. J Colloid Interface Sci. 292: 71-8. PMID: 15978605
- Coupled surface-enhanced Raman spectroscopy and electrical conductivity measurements of 1,4-phenylene diisocyanide in molecular electronic junctions. | Jaiswal, A., et al. 2006. Anal Chem. 78: 120-4. PMID: 16383318
- Surface-enhanced Raman spectroscopic study of 1,4-phenylene diisocyanide adsorbed on gold and platinum-group transition metal electrodes. | Gruenbaum, SM., et al. 2006. J Phys Chem B. 110: 4782-92. PMID: 16526715
- Chemical stability and characterization of rhodium-diisocyanide coordination polymers. | Carson, CG., et al. 2007. J Phys Chem B. 111: 14114-20. PMID: 18047318
- Cooperativity of cytochrome P450 1A2: interactions of 1,4-phenylene diisocyanide and 1-isopropoxy-4-nitrobenzene. | Isin, EM., et al. 2008. Arch Biochem Biophys. 473: 69-75. PMID: 18328798
- Linking gold nanoparticles with conductive 1,4-phenylene diisocyanide-gold oligomers. | Kestell, J., et al. 2013. Chem Commun (Camb). 49: 1422-4. PMID: 23310932
- Unidirectional Adsorption of Bifunctional 1,4-Phenylene Diisocyanide on the Ge(100)-2 × 1 Surface. | Shong, B., et al. 2015. J Phys Chem Lett. 6: 1037-41. PMID: 26262866
- Determination of Adsorbate Structures from 1,4-Phenylene Diisocyanide on Gold. | Kestell, J., et al. 2014. J Phys Chem Lett. 5: 3577-81. PMID: 26278612
- Cooperative Chemisorption-Induced Physisorption of CO2 Molecules by Metal-Organic Chains. | Feng, M., et al. 2015. ACS Nano. 9: 12124-36. PMID: 26548479
- Nanostructuring of Au(111) during the Adsorption of an Aromatic Isocyanide from Solution. | Ghalgaoui, A., et al. 2017. Langmuir. 33: 91-99. PMID: 27996271
- Bimetallic Au@M (M = Ag, Pd, Fe, and Cu) Nanoarchitectures Mediated by 1,4-Phenylene Diisocyanide Functionalization. | Kang, JS., et al. 2018. Langmuir. 34: 2849-2855. PMID: 29400974
- Chemical self-assembly strategies for designing molecular electronic circuits. | Olson, D., et al. 2019. Chem Commun (Camb). 55: 13872-13875. PMID: 31674624
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
1,4-Phenylene diisocyanide, 1 g | sc-223061 | 1 g | $315.00 |