Apr 29, 2024 · butanoyl chloride - cas 141-75-3, synthesis, structure, density, melting point, boiling point

Butanol (also called butyl alcohol) is a four-carbon alcohol with a formula of C 4 H 9 OH, which occurs in five isomeric structures (four structural isomers), from a straight-chain primary alcohol to a branched-chain tertiary alcohol; [1] all are a butyl or isobutyl group linked to a hydroxyl group (sometimes represented as BuOH, sec-BuOH, i-BuO...

Butyryl chloride is an organic compound with the chemical formula CH 3 CH 2 CH 2 C (O)Cl. It is a colorless liquid with a unpleasant odor. Butyryl chloride is soluble in organic solvents, but it reacts readily with water and alcohols. It is usually produced by chlorination of butyric acid. [1]

IUPAC Standard InChI: InChI=1S/C4H7ClO/c1-2-3-4(5)6/h2-3H2,1H3 Copy IUPAC Standard InChIKey: DVECBJCOGJRVPX-UHFFFAOYSA-N Copy CAS Registry Number: 141-75-3 Chemical ...

Butyryl chloride appears as a clear colorless liquid with a sharp odor. Slightly denser than water. Flash point near 20 °F. Severely irritates skin, eyes, and mucous membranes. Used to make other chemicals. butanoyl chloride. Computed by Lexichem TK 2.7.0 (PubChem release 2021.10.14) InChI=1S/C4H7ClO/c1-2-3-4 (5)6/h2-3H2,1H3.

May 7, 2021 · (111C)butanoyl chloride | C4H7ClO | CID 451289 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.

Butanoyl chloride, 2-methyl- | C5H9ClO | CID 93697 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.

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Butyryl chloride is a colorless to light yellow liquid with a strong pungent odor. It undergoes vigorous hydrolysis with water; decomposes in water; soluble in almost aprotic organic solvents. It is used as an intermediate for organic synthesis for the preparation of pharmaceuticals, agrochemicals, dyes, cellulose esters, and peroxide compounds.

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