propylenediamine (CHEBI:30630) - EMBL-EBI
A diamine that is propane substituted by amino groups at positions 1 and 2. Propylenediamine is commonly used as a bidentate ligand in the formation of coordination complexes. This entity has been manually annotated by the ChEBI Team. 1,2-Diaminopropane (propane-1,2-diamine) is organic compound with the formula CH3CH (NH2)CH2NH2.
1,3-Diaminopropane - Wikipedia
1,3-Diaminopropane, also known as trimethylenediamine, is a simple diamine with the formula H 2 N (CH 2) 3 NH 2. A colourless liquid with a fishy odor, it is soluble in water and many polar organic solvents. It is isomeric with 1,2-diaminopropane.
1,2-丙二胺 - 百度百科
1,2-丙二胺，是一种有机化合物，化学式为C3H10N2，用于有机合成、制药及合成染料，并用作溶纤剂、橡胶硫化促进剂等。
1,2-Diaminopropane - Wikipedia
1,2-Diaminopropane (propane-1,2-diamine) is organic compound with the formula CH 3 CH (NH 2)CH 2 NH 2. A colorless liquid, it is the simplest chiral diamine. It is used as a bidentate ligand in coordination chemistry. Industrially, this compound is synthesized by the ammonolysis of 1,2-dichloropropane: [1]
1,2-Diaminopropane | C3H10N2 | CID 6567 - PubChem
Propylenediamine is a diamine that is propane substituted by amino groups at positions 1 and 2. Propylenediamine is commonly used as a bidentate ligand in the formation of coordination complexes. It has a role as a ligand.
Propylene-1,2-diamine | C3H8N2 | CID 18986484 - PubChem
Propylene-1,2-diamine | C3H8N2 | CID 18986484 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.
1,2-Propylenediamine | CAS No.:78-90-0 - BASF
As a building block, 1,2-Propylenediamine is a raw material for the production of polyurethane resins (polyester polyol and polycarbonate diol). It provides a balance between hardness and flexibility, adhesion, weatherability and hydrolysis resistance. It is also used as a chain extender in the production of polyurethane dispersions.
Propylenediamine - an overview | ScienceDirect Topics
The N-substituted ethylenediamines and propylenediamines can be prepared, according to Goodwin and Lions, 1 by the reaction of the diamine with the appropriate aldehyde followed by the reduction of enamine by zinc dust, MBH 4 (M = Na, K), or hydrogen with Pt/C catalyst.
1,2-Propanediamine - NIST Chemistry WebBook
IUPAC Standard InChI: InChI=1S/C3H10N2/c1-3(5)2-4/h3H,2,4-5H2,1H3 Copy IUPAC Standard InChIKey: AOHJOMMDDJHIJH-UHFFFAOYSA-N Copy CAS Registry Number: 78-90-0 Chemical ...
1,2-Propanediamine - NIST Chemistry WebBook
Wincel, H.; Herman, J.A., Photoionization Study of Clustering Reactions in Diamines: Ethane-1,2-diamine, Propane-1,2-diamine and Propane-1,3-diamine, J. Chem. Soc. Faraday Trans., 1973, 69, 1797, https://doi.org/10.1039/f19736901797.