
CAS 1188535-10-5
:1,3-PROPANEDIAMINE, N1-(3,4-DICHLOROPHENYL)-
Description:
1,3-Propanediamine, N1-(3,4-dichlorophenyl)- is an organic compound characterized by its amine functional groups and a dichlorophenyl substituent. This compound features a three-carbon straight-chain backbone with two amine (-NH2) groups located at the terminal positions, which contributes to its basicity and potential reactivity in various chemical reactions. The presence of the 3,4-dichlorophenyl group introduces significant steric and electronic effects, influencing the compound's solubility, reactivity, and potential applications in pharmaceuticals or agrochemicals. Typically, such compounds may exhibit properties like moderate to high polarity due to the amine groups, and they may participate in hydrogen bonding, affecting their physical state and interactions with other substances. Safety data sheets would indicate that handling requires caution due to potential toxicity or irritant effects associated with amines and halogenated compounds. Overall, this compound's unique structure makes it a subject of interest in synthetic organic chemistry and material science.
Formula:C9H12Cl2N2
Synonyms:- N1-(3,4-Dichlorophenyl)-1,3-propanediamine
- 1,3-PROPANEDIAMINE, N1-(3,4-DICHLOROPHENYL)-
- N1-
- dichlorophenyl)
- N'-(3,4-dichlorophenyl)propane-1,3-diamine
- - 1,
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N1-(3,4-Dichlorophenyl)-1,3-propanediamine
CAS:Controlled Product<p>Applications N1-(3,4-Dichlorophenyl)-1,3-propanediamine is a compound being used in the synthesis of novel amide-based biaryl complexes which can act as allosteric binding site antagonists of NR1A/NR2B NMDA receptors.<br>References Mosley, C.A., et al.: Bioorg. Med. Chem. Lett., 17, 6463-6480 (2009)<br></p>Formula:C9H12Cl2N2Color and Shape:NeatMolecular weight:219.111
