2-(Diisopropylamino)ethylthiourea is an organic compound characterized by the presence of a thiourea functional group, which consists of a carbon atom double-bonded to sulfur and single-bonded to an amine group. This compound features a diisopropylamino substituent, indicating that it has two isopropyl groups attached to a nitrogen atom, contributing to its steric bulk and potentially influencing its reactivity and solubility. The ethyl chain connects the thiourea moiety to the diisopropylamino group, providing a flexible structure that may facilitate interactions with biological targets or other chemical species. Typically, compounds like this can exhibit properties such as moderate to high solubility in organic solvents, and they may participate in hydrogen bonding due to the presence of the thiourea and amine functionalities. The compound's unique structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals or agrochemicals, although specific biological activities would require further investigation. Safety and handling precautions should be observed, as with any chemical substance, due to potential toxicity or reactivity.

2-(diisopropylamino)ethylthiourea

886363-52-6: 2-(Diisopropylamino)ethylthiourea is an organic compound characterized by the presence of a thiourea functional group, which consists of a carbon atom double-bonded to sulfur and single-bonded to an amine group. This compound features a diisopropylamino substituent, indicating that it has two isopropyl groups attached to a nitrogen atom, contributing to its steric bulk and potentially influencing its reactivity and solubility. The ethyl chain connects the thiourea moiety to the diisopropylamino group, providing a flexible structure that may facilitate interactions with biological targets or other chemical species. Typically, compounds like this can exhibit properties such as moderate to high solubility in organic solvents, and they may participate in hydrogen bonding due to the presence of the thiourea and amine functionalities. The compound's unique structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals or agrochemicals, although specific biological activities would require further investigation. Safety and handling precautions should be observed, as with any chemical substance, due to potential toxicity or reactivity.

CAS 886363-52-6

2-(diisopropylamino)ethylthiourea

Thiourea,N-[2-[bis(1-methylethyl)amino]ethyl]-

Ref: IN-DA004AP1

(2-Diisopropylamino-ethyl)-thiourea

Ref: 10-F040545