CAS 5544-35-4

N-(Aminocarbonyl)-3-chloropropanamide

Description:

N-(Aminocarbonyl)-3-chloropropanamide, with the CAS number 5544-35-4, is an organic compound characterized by its amide functional group and a chlorinated propanamide structure. This compound features a carbonyl group (C=O) directly attached to a nitrogen atom, which is also linked to a 3-chloropropyl chain. The presence of the chlorine atom introduces unique reactivity and polarity, influencing its solubility and interaction with other chemical species. Typically, compounds of this nature exhibit moderate to high solubility in polar solvents due to their ability to form hydrogen bonds. They may also participate in various chemical reactions, including nucleophilic substitutions and acylation processes. The compound's biological activity can vary, making it of interest in pharmaceutical and agrochemical research. Safety data should be consulted for handling and storage, as halogenated compounds can pose specific health and environmental risks. Overall, N-(Aminocarbonyl)-3-chloropropanamide is a versatile compound with potential applications in synthetic chemistry and medicinal chemistry.

Formula: C₄H₇ClN₂O₂

InChI: InChI=1S/C4H7ClN2O2/c5-2-1-3(8)7-4(6)9/h1-2H2,(H3,6,7,8,9)

InChI key: InChIKey=HRYUUBFCDGPNLW-UHFFFAOYSA-N

SMILES: N(C(CCCl)=O)C(N)=O

Synonyms:

• (3-Chloropropanoyl)urea
• 1-(3-Chloropropionyl)urea
• N-(aminocarbonyl)-3-chloropropanamide
• Propanamide, N-(aminocarbonyl)-3-chloro-
• Urea, (3-chloropropionyl)-

(3-Chloropropanoyl)urea

CAS: 5544-35-4

3-Chloropropanoyl)urea is a urea derivative. It has been used as an intermediate in the synthesis of tranquilizers and reaction products. 3-Chloropropanoyl)urea has been shown to react with aliphatic hydrocarbons, cycloaliphatic compounds, piperidine, or acylurea. The resulting products are chlorinated or carboxylic acid derivatives.

Formula: C₄H₇ClN₂O₂

Purity: Min. 95%

Molecular weight: 150.56 g/mol

Ref: 3D-FAA54435