Welcome to LookChem.com Sign In|Join Free
  • or
1,3-Bis(1-imidazolyl)propane, also known as TRIP, is a tridentate ligand with the chemical formula C11H14N4. It is a versatile molecule that can bind to metal ions in three places, making it a valuable component in coordination chemistry. TRIP is widely used in organic synthesis and catalysis, particularly for the formation of C–C and C–N bonds. Its applications extend to the preparation of metal complexes for use in photophysics and material science, as well as potential pharmaceutical applications, including antibacterial and antiviral properties.

69506-85-0

Post Buying Request

69506-85-0 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

69506-85-0 Usage

Uses

Used in Coordination Chemistry:
1,3-BIS(1-IMIDAZOLYL)PROPANE is used as a tridentate ligand for binding to metal ions in coordination chemistry, facilitating the formation of stable metal complexes.
Used in Organic Synthesis:
1,3-BIS(1-IMIDAZOLYL)PROPANE is used as a catalyst in organic synthesis for the formation of C–C and C–N bonds, enhancing the efficiency and selectivity of various chemical reactions.
Used in Photophysics:
1,3-BIS(1-IMIDAZOLYL)PROPANE is used in the preparation of metal complexes for photophysical applications, such as luminescent materials and sensors, due to its ability to influence the electronic properties of the complexes.
Used in Material Science:
1,3-BIS(1-IMIDAZOLYL)PROPANE is used in the development of metal complexes for material science applications, including the creation of new materials with unique properties and functions.
Used in Pharmaceutical Applications:
1,3-BIS(1-IMIDAZOLYL)PROPANE is used as a potential pharmaceutical candidate for its antibacterial and antiviral properties, offering new avenues for the development of therapeutic agents.
Used in Antibacterial Applications:
1,3-BIS(1-IMIDAZOLYL)PROPANE is used as an antibacterial agent, targeting and inhibiting the growth of various bacteria, providing a potential alternative to conventional antibiotics.
Used in Antiviral Applications:
1,3-BIS(1-IMIDAZOLYL)PROPANE is used as an antiviral agent, exhibiting activity against a range of viruses, offering potential therapeutic benefits in the treatment of viral infections.

Check Digit Verification of cas no

The CAS Registry Mumber 69506-85-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,5,0 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 69506-85:
(7*6)+(6*9)+(5*5)+(4*0)+(3*6)+(2*8)+(1*5)=160
160 % 10 = 0
So 69506-85-0 is a valid CAS Registry Number.

69506-85-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[3-(1H-imidazol-1-yl)propyl]-1H-imidazole

1.2 Other means of identification

Product number -
Other names 1,1'-(1,3-propanediyl)bis(imidazole)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:69506-85-0 SDS

69506-85-0Relevant academic research and scientific papers

Tetrakis(imidazolium) macrocyclic receptors for anion binding

Wong, Wallace W. H.,Vickers, Matthew S.,Cowley, Andrew R.,Paul, Rowena L.,Beer, Paul D.

, p. 4201 - 4208 (2005)

New (tetrakis)imidazolium macrocyclic receptor systems of variable cavity size have been synthesised by stepwise alkylation reactions of bis(imidazolium) precursor compounds. Proton NMR titration studies reveal the macrocycles to strongly bind halide and benzoate anions, with two receptor systems displaying notable selectivity for fluoride in competitive acetonitrile-water (9:1) solvent media. The Royal Society of Chemistry 2005.

Syntheses and structural characterization of Cu(II) and Mn(II) coordination polymers with the neutral flexible bidentate N-donor ligands

Lalegani, Arash,Khaledi Sardashti, Mohammad,Khalaj, Mehdi,Gajda, Roman,Wo?niak, Krzysztof

, p. 136 - 144 (2017)

Four new coordination polymers of [Cu(μ-bip)2(N3)2·2H2O]n(1), [Cu(μ-bbd)2(μ4-N3)4]n(2), [Mn(μ-bip)2(NCS)2]n(3) and [Mn(μ-bip)2(N3)2]n(4) were prepared by using the neutral N-donor ligands 1,3-bis(imidazolyl)propane (bip) and 1,4-bis(3,5-dimethylpyrazolyl)butane (bbd), mono-anionic NCS?or N3?ligands and appropriate metal salts of Cu(II) and Mn(II) ions. The results of the X-ray measurements demonstrate that in the crystal structure of 1, 3 and 4 the metal ions adopts MN6(M = Cu, Mn) an octahedral geometry while, in the structure of 2, the copper(II) ion forms CuN5trigonal bipyramides. In the polymer 1, 3 and 4 the N3?or NCS?groups are terminally bonded to the metal center and each bip ligand with anti-gauche conformation acts as bridging ligand connecting two metal ions to form a one-dimensional zig-zag chain. Whereas in the polymer 2, the N3groups adopt so called End-on mode of connection with metal center and the each bbd with anti-anti-anti conformation acts as bridging connecting two copper(II) ions to form a two-dimensional network with a hcb [point symbol (36)] topology. Compounds 1, 3 and 4 are isostructural with each other.

Homoleptic crown N-heterocyclic carbene complexes

McKie, Ross,Murphy, John A.,Park, Stuart R.,Spicer, Mark D.,Zhou, Sheng-Ze

, p. 6525 - 6528 (2007)

(Figure Presented) Two ways about it: The first metal N-heterocyclic carbene complexes derived from a cyclic tetraimidazolium salt show a remarkable versatility of ligand conformation and coordination geometry. With Pd II, a mononuclear square-planar complex is obtained, but with Cu I and AgI, an unprecedented dinuclear motif with a short metal-metal interaction is observed (see structure; N blue, C white ellipsoids, H white circles).

Reactivity of Ruthenium(II) Complexes Bearing Bis-NHC Ligands

Dutschke, Patrick D.,Hahn, F. Ekkehardt,Hepp, Alexander,Lübbering, Tobias

supporting information, p. 3775 - 3784 (2021/11/17)

Bis-imidazolium salts bearing N-2-fluorobenzyl substituents and methylene, ethylene, or propylene linkers ([H2-4]Br2-[H2-6]Br2) and the bis-imidazolium salt [H2-8]Br2 featuring an ethylene linker and N-3-fluorophenyl substituents have been prepared. Salts [H2-5]Br2 and [H2-6]Br2 react with [RuCl2(CO)2]n to give the bis-NHC chelate complexes [9] and [10]. Chloride substitution in [10] for the 2-nitrophenyl isocyanide ligand 11 yielded the complex [12]PF6. The nitro group of the isocyanide in [12]PF6 could not be reduced. Salts [H2-4]Br2 and [H2-5]Br2 yield with [RuCp*(MeCN)3]PF6 the chelate complexes [13]PF6 and [14]PF6, respectively. The propylene-bridged bis-imidazolium salt [H2-6]Br2 reacts with [RuCp*(MeCN)3]PF6 to give, via an oxidative addition of a C-H bond of the central methylene group of the linker, the seven-coordinate RuIV complex [15]PF6 bearing a tridentate CNHCCalkylCNHC ligand and a hydrido ligand. Introduction of a nitrophenyl isocyanide ligand to [14]PF6 and reduction of the nitro group to the primary amine was also possible. Finally, [H2-8]Br2 reacts with [RuCp*(MeCN)3]PF6 to give, after intramolecular oxidative addition of a Caryl-H bond followed by reductive elimination of an imidazolium group, the complex [20]PF6 bearing a unique tridentate CarylCNHCC=Cimidazolium chelate ligand.

Catalytic assay of Schiff base Co(II), Ni(II), Cu(II) and Zn(II) complexes for N-alkylation of heterocycles with 1,3-dibromopropane

Chavan, Sanjay,Gaikwad, Gautam,Hegade, Sujit,Jadhav, Yuvraj,Mulik, Ganpatrao

, (2020/08/06)

Abstract: N-alkylation of heterocycles with 1,3-dibromopropane using Schiff base Co(II), Ni(II), Cu(II) and Zn(II) transition metal complexes as a catalyst was studied in 1:1 and 2:1 coupling ratios under mild conditions. It was observed that all the complexes worked as efficient catalyst with product yield 78–92percent for coupling ratio 1:1 and product yield 63–78percent for coupling ratio 2:1. N-alkylation of heterocycles with 1,3-dibromopropane in 1:1 coupling ratio is easier with higher yields as compared with N-alkylation in 2:1 coupling ratio. Graphic abstract: N-Alkylation of heterocycles with 1,3-dibromopropane[Figure not available: see fulltext.]

A amino-containing double-nuclear alkaline ionic liquid and its preparation method and application

-

Paragraph 0035; 0036; 0037, (2017/09/26)

The invention discloses a novel amino-containing dual-core basic ionic liquid and a preparation method and an application thereof. The structure formula of the ionic liquid is as shown in the description, wherein n is 2, 3, 4, 5 or 6. The ionic liquid disclosed by the invention reacts with a bromine salt by virtue of a dual-core substance; the obtained substance contains a plurality of amino groups, is relatively high in alkalinity and relatively good in effect on carbon dioxide absorption, and can be repeatedly used for a plurality of times.

Synthesis and properties of dicationic ionic liquids containing a siloxane structural moiety

Glukhov,Krasovskiy,Chernikova,Kapustin,Kustov,Koroteev

, p. 2204 - 2209 (2015/11/17)

Five new ionic liquids formed by doubly charged cations containing a siloxane moiety and bis(trifluoromethylsulfonyl) imide anion are synthesized and characterized. Their thermal stability is studied by means of TGA; melting points (glass transition temperatures) and densities are measured. The temperature dependences of kinematic viscosity of the obtained ionic liquids are presented along with their approximations by the Vogel-Tammann-Fulcher equation.

Synthesis and antitubercular screening of imidazole derivatives

Pandey, Jyoti,Tiwari, Vinod K.,Verma, Shyam S.,Chaturvedi, Vinita,Bhatnagar,Sinha,Gaikwad,Tripathi, Rama P.

experimental part, p. 3350 - 3355 (2009/12/01)

A series of imidazole based compounds were synthesized by reacting simple imidazoles with alkyl halides or alkyl halocarboxylate in presence of tetrabutylammonium bromide (TBAB). The compounds bearing carbethoxy group undergo amidation with different amines in the presence of DBU to give respective carboxamides. The synthesized compounds were screened against Mycobacterium tuberculosis where compound 17 exhibited very good in vitro antitubercular activity and may serve as a lead for further optimization.

Size selective recognition of anions by a tetracationic imidazoliophane

Sato, Kiyoshi,Onitake, Tomomi,Arai, Sadao,Yamagishi, Takamichi

, p. 779 - 784 (2007/10/03)

The reaction of 1:1 mixture of 1,3-bis(1-imidazolyl)propane and 1,4-bis(chloromethyl)durene gives a new tetracationic heterophane (2), which forms a 1:1 inclusion complex with halides and oxoanions in DMSO-d6 in the order of HSO4- > Br- > H2PO4- > Cl- > I- > ClO4- depending on the size of anions.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 69506-85-0