1-[4-(Propan-2-yl)phenyl]-3-prop-2-en-1-ylthiourea, with the CAS number 889221-30-1, is an organic compound characterized by its thiourea functional group, which is known for its diverse biological activities. This compound features a substituted phenyl ring, specifically a para-isopropyl group, contributing to its hydrophobic properties and potential interactions in biological systems. The presence of the prop-2-en-1-yl group introduces a double bond, which may enhance its reactivity and ability to participate in various chemical reactions, such as nucleophilic additions or polymerization processes. The thiourea moiety is often associated with applications in medicinal chemistry, as it can exhibit antitumor, antifungal, and antibacterial properties. Additionally, the compound's structural features suggest potential for use in agrochemicals or as a building block in organic synthesis. Its solubility, stability, and reactivity would depend on the specific conditions, including solvent and temperature, making it a subject of interest for further research in both synthetic and applied chemistry.

1-[4-(propan-2-yl)phenyl]-3-prop-2-en-1-ylthiourea

889221-30-1: 1-[4-(Propan-2-yl)phenyl]-3-prop-2-en-1-ylthiourea, with the CAS number 889221-30-1, is an organic compound characterized by its thiourea functional group, which is known for its diverse biological activities. This compound features a substituted phenyl ring, specifically a para-isopropyl group, contributing to its hydrophobic properties and potential interactions in biological systems. The presence of the prop-2-en-1-yl group introduces a double bond, which may enhance its reactivity and ability to participate in various chemical reactions, such as nucleophilic additions or polymerization processes. The thiourea moiety is often associated with applications in medicinal chemistry, as it can exhibit antitumor, antifungal, and antibacterial properties. Additionally, the compound's structural features suggest potential for use in agrochemicals or as a building block in organic synthesis. Its solubility, stability, and reactivity would depend on the specific conditions, including solvent and temperature, making it a subject of interest for further research in both synthetic and applied chemistry.

CAS 889221-30-1

1-[4-(propan-2-yl)phenyl]-3-prop-2-en-1-ylthiourea

3-(prop-2-en-1-yl)-1-[4-(propan-2-yl)phenyl]thiourea

Ref: IN-DA00GTXJ

1-Allyl-3-(4-isopropylphenyl)thiourea

Ref: 54-OR89756

1-Allyl-3-(4-isopropylphenyl)thiourea

Ref: 10-F787751