Phenylisocyanide | C7H5N | CID 13606 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety ...

2024年4月29日 · Phenyl isocyanate - cas 103-71-9, synthesis, structure, density, melting point, boiling point

Temperature (K) A B C Reference Comment; 285. to 438. 4.56096: 1800.567-42.985: Stull, 1947: Coefficents calculated by NIST from author's data.

Phenyl isocyanide is a compound that plays a key role in coordination chemistry, particularly in the formation of carbene complexes with specific ligands, depending on the metal fragment attached. You might find these chapters and articles relevant to this topic.

Chemical Entities of Biological Interest (ChEBI) is a freely available dictionary of molecular entities focused on 'small' chemical compounds.

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Phenyl isocyanate is an organic compound typically abbreviated PhNCO. The molecule consists of a phenyl ring attached to the isocyanate functional group. It is a colourless liquid that reacts with water. Phenyl isocyanate has a strong odor and tearing vapours, therefore it has to be handled with care.

An isocyanide (also called isonitrile or carbylamine) is an organic compound with the functional group – N + ≡C −.It is the isomer of the related nitrile (–C≡N), hence the prefix is isocyano. [1] The organic fragment is connected to the isocyanide group through the nitrogen atom, not via the carbon.They are used as building blocks for the synthesis of other compounds.

Phenyl isocyanide, also known as benzonitrile, is a colorless liquid with a sharp, unpleasant odor resembling that of bitter almonds. It is highly volatile and can be easily detected by its distinctive smell.

ChemSpider record containing structure, synonyms, properties, vendors and database links for Isocyanobenzene, 931-54-4, RCIBIGQXGCBBCT-UHFFFAOYSA-N