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5036-48-6 | 1-(3-Aminopropyl)imidazole
CAS No: 5036-48-6 Catalog No: AG0035AE MDL No:MFCD00009819
Product Description
Catalog Number:
AG0035AE
Chemical Name:
1-(3-Aminopropyl)imidazole
CAS Number:
5036-48-6
Molecular Formula:
C6H11N3
Molecular Weight:
125.1716
MDL Number:
MFCD00009819
IUPAC Name:
3-imidazol-1-ylpropan-1-amine
InChI:
InChI=1S/C6H11N3/c7-2-1-4-9-5-3-8-6-9/h3,5-6H,1-2,4,7H2
InChI Key:
KDHWOCLBMVSZPG-UHFFFAOYSA-N
SMILES:
NCCCn1cncc1
EC Number:
225-730-9
Properties
Complexity:
74.7
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
125.095g/mol
Formal Charge:
0
Heavy Atom Count:
9
Hydrogen Bond Acceptor Count:
2
Hydrogen Bond Donor Count:
1
Isotope Atom Count:
0
Molecular Weight:
125.175g/mol
Monoisotopic Mass:
125.095g/mol
Rotatable Bond Count:
3
Topological Polar Surface Area:
43.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-0.6
Literature
| Title | Journal |
|---|---|
| Synthesis and DNA binding properties of 1-(3-aminopropyl)-imidazole-containing triamide f-Im*PyIm: a novel diamino polyamide designed to target 5'-ACGCGT-3'. | Bioorganic & medicinal chemistry letters 20120915 |
| Paclitaxel loaded nano-aggregates based on pH sensitive polyaspartamide amphiphilic graft copolymers. | International journal of pharmaceutics 20120315 |
| Spectral, biological screening of metal chelates of chalcone based Schiff bases of N-(3-aminopropyl) imidazole. | Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20120215 |
| pH-Sensitive micelles with cross-linked cores formed from polyaspartamide derivatives for drug delivery. | Langmuir : the ACS journal of surfaces and colloids 20111004 |
| Bioreducible polymers with cell penetrating and endosome buffering functionality for gene delivery systems. | Journal of controlled release : official journal of the Controlled Release Society 20110530 |
| Application of molecular topology for the prediction of reaction yields and anti-inflammatory activity of heterocyclic amidine derivatives. | International journal of molecular sciences 20110101 |
| Effect of hydrophobic octadecyl groups on pH-sensitive aggregation behavior of imidazole-containing polyaspartammide derivatives. | Journal of nanoscience and nanotechnology 20101001 |
| Conventional and microwave assisted synthesis of small molecule based biologically active heterocyclic amidine derivatives. | European journal of medicinal chemistry 20100301 |
| One pot synthesis of pyrimidine and bispyrimidine derivatives and their evaluation for anti-inflammatory and analgesic activities. | Bioorganic & medicinal chemistry 20070515 |
| Phase transition behavior of novel pH-sensitive polyaspartamide derivatives grafted with 1-(3-aminopropyl)imidazole. | Macromolecular bioscience 20060915 |
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