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1H-Imidazolium, 1,1'-methylenebis[3-(1,1-dimethylethyl)-, dibromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

247902-48-3

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247902-48-3 Usage

Composition

Two 1,1'-methylenebis[3-(1,1-dimethylethyl)-1H-Imidazolium units.

Central structure

Each unit contains a central imidazole ring.

Dibromide

Contains two bromine atoms.

Application

Used as a reactant in organic synthesis.

Antimicrobial properties

Useful in pharmaceutical and medical applications.

Potential as an ionic liquid

Studied for use as a solvent or electrolyte in chemical processes.

Versatility

Valuable component in various industrial and scientific fields.

1H-Imidazolium

Refers to the central imidazole ring structure in each unit.

Methylene bridge

Connects the two 1H-Imidazolium units via a methylene group (-CH2-).

1,1-Dimethylethyl group

A bulky alkyl group (C8H17) attached to the 3-position of the imidazole ring.

Dibromide functionality

Two bromine atoms (Br) attached to the 3-position of the imidazole ring, enhancing the compound's reactivity and properties.

Organic synthesis

The compound can be used as a building block or intermediate in the synthesis of more complex organic molecules.

Pharmaceutical and medical applications

The antimicrobial properties make it suitable for use in disinfectants, antibiotics, or other medical treatments.

Ionic liquid research

The compound's potential as an ionic liquid is being explored for its use as a green solvent or electrolyte in various chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 247902-48-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,7,9,0 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 247902-48:
(8*2)+(7*4)+(6*7)+(5*9)+(4*0)+(3*2)+(2*4)+(1*8)=153
153 % 10 = 3
So 247902-48-3 is a valid CAS Registry Number.

247902-48-3 Well-known Company Product Price

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  • TCI America

  • (M2790)  3,3'-Methylenebis(1-tert-butyl-3-imidazolium Bromide)  >98.0%(N)

  • 247902-48-3

  • 1g

  • 350.00CNY

  • Detail
  • TCI America

  • (M2790)  3,3'-Methylenebis(1-tert-butyl-3-imidazolium Bromide)  >98.0%(N)

  • 247902-48-3

  • 5g

  • 1,390.00CNY

  • Detail

247902-48-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3'-Methylenebis(1-tert-butyl-3-imidazolium Bromide)

1.2 Other means of identification

Product number -
Other names Isothiocyanic Acid Benzyl Ester

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:247902-48-3 SDS

247902-48-3Downstream Products

247902-48-3Relevant academic research and scientific papers

Organoplatinum(ii) complexes containing chelating or bridging bis(N-heterocyclic carbene) ligands: Formation of a platinum(ii) carbonate complex by aerial CO2 fixation

Jamali, Sirous,Milic, Dalibor,Kia, Reza,Mazloomi, Zahra,Abdolahi, Hallimeh

, p. 9362 - 9365 (2011)

The preparation of two new bis(N-heterocyclic carbene) platinum(ii) complexes, in which NHC rings are joined by a CH2 linker group, is described. While, the chelate complex [PtMe2(bis-NHC1)], 1, was formed with large tert-butyl wingtips, the iso-propyl N-substituent analogue favors formation of the cluster complex [Pt2Me4(μ- SMe2)(μ-bis-NHC2)]2(μ-Ag2Br2), 2, in which two binuclear platinum(ii) complexes are linked together by an Ag2Br2 unit. The chelating platinum complex 1 undergoes aerial CO2 fixation and forms platinum(ii) carbonate complex [Pt(CO3)(bis-NHC1)], 3.

Carbene-anchored/pendent-imidazolium species as precursors to di-N-heterocyclic carbene-bridged mixed-metal complexes

Zamora, Matthew T.,Ferguson, Michael J.,McDonald, Robert,Cowie, Martin

, p. 7269 - 7287 (2009)

Reaction of a series of linked diimidazolium dibromide salts with one-half equivalent of [Rh(μ-OAc)(COD)]2 under reflux conditions generates a series of carbene-anchored/pendent-imidazolium complexes, [RhBr(COD)( RC(H)-η1-Ceth)][Br] (MeC(H)- η1-Ceth = ethylene[(N-methyl)imidazolium][(N-methyl) imidazole-2-ylidene] and tBuC(H)-η1-Ceth = ethylene[(N-tert-butyl)imidazolium][(N-tert-butyl)imidazole-2-ylidene]) via deprotonation of one end of the diimidazolium salt and coordination of the resulting carbene to Rh. Reaction of these complexes with carbon monoxide or the appropriate diphosphine yields either [RhBr(CO)2( RC(H)-η1-Ceth)][Br] (R = Me, tBu) or [RhBr(P∩P)(MeC(H)- η1-Ceth)][Br] (P∩P = Ph 2PCH2PPh2, Ph2PCH2CH 2PPh2, Et2PCH2PEt2), respectively. The resulting diphosphine complexes readily decompose in solution. A series of palladium complexes [PdI3-n(PR3) n(L)][I]n (n = 1,2) and [PdI(P∩P)(L)][I] 2 (L = tBuC(H)-η1-Cmeth, tBuC(H)-η1-Ceth; tBuC(H)- η1-Cmeth = methylene[(N-tert-butyl)imidazolium][(N- tert-butyl)imidazole-2-ylidene]), containing the linked NHC-imidazolium moiety, have also been prepared by reacting the triiodo complexes, [PdI 3(tBuC(H)-η1-Cmeth)] and [PdI3(tBuC(H)-η1-Ceth)] with several mono- and diphosphines. Attempts to generate mixed Rh/Pd complexes using Pd(OAc)2 to deprotonate the pendent arm of several of the above carbene-anchored/pendent-imidazolium complexes of Rh have proven unsuccessful. However, a targeted di-NHC-bridged heterobimetallic complex [PdI 2(PEt3)(μ-tBuCCmeth)RhI(COD)] (tBu CCmeth = 1,1′-methylene-3,3′-di-tert- butyldiimidazol-2,2′-diylidene) can be generated by deprotonation of the imidazolium group in [PdI2(PEt3)(tBuC(H)- η1-Cmeth)][I] using half an equivalent of [Rh(μ-OAc)(COD)]2. The X-ray structure determination of this Pd/Rh complex confirms the dicarbene-bridged formulation and shows a metal-metal separation of approximately 6.2 A. Reaction of this Rh/Pd complex with CO yields the corresponding dicarbonyl product [PdI2(PEt 3)(μ-tBuCCmeth)RhI(CO)2] via replacement of the COD ligand. The related dicarbene-bridged Ir/Rh complex [IrBr(COD)(μ-tBuCCmeth)RhBr(COD)] can be generated by reaction of [IrBr(COD)(tBuC(H)-η1-Cmeth)] [Br] with [Rh(μ-OAc)(COD)]2, while the Pd/Ir complexes [PdI 2(PR3)(μ-tBuCCmeth)IrI(COD)] (PR3 = PPh3, PMe2Ph) can be generated by reaction of the monometallic [PdI2(PR3)( tBuC(H)-η1-Cmeth)][I] species with K[N(SiMe3)2] in the presence of [Ir(μ-Cl)(COD)] 2. The carbonyl analogues, [PdI2(PR3)(μ- tBuCCmeth)IrI(CO)2], can be generated via a gentle purge of CO gas. These di-NHC-bridged heterobimetallic species represent some of the first examples of this class and are the first involving palladium.

Bis-NHC chelate complexes of nickel(0) and platinum(0)

Brendel, Matthias,Braun, Carolin,Rominger, Frank,Hofmann, Peter

, p. 8741 - 8745 (2014)

For a long time d10-ML2 fragments have been known for their potential to activate unreactive bonds by oxidative addition. In the development of more active species, two approaches have proven successful: the use of strong σ-donating

USE OF PT-AND PD-BIS-AND TETRA-CARBON COMPLEXES WITH BRIDGED CARBON LIGANDS IN OLEDS

-

Page/Page column 10; 11, (2010/01/31)

The use of Pt- and Pd-bis- and tetracarbene complexes with bridged carbene ligands in organic light-emitting diodes, organic light-emitting diodes comprising at least one aforementioned Pt- or Pd-carbene complex, at least one transition metal-carbene comp

Bridged imidazolium salts used as precursors for chelating carbene complexes of palladium in the Mizoroki-Heck reaction

Scherg, Tobias,Schneider, Sabine K.,Frey, Guido D.,Schwarz, Jürgen,Herdtweck, Eberhardt,Herrmann, Wolfgang A.

, p. 2894 - 2907 (2008/03/13)

A variety of chiral and achiral imidazolium salts is synthesized. Methylene-, ethylene-, propylene- and pyridinyl-bridged bis(imidazolium) halides are used to generate the respective free chelating carbenes. The synthesis of palladium complexes of general formula [cis-CH2{NC(H)=C(H)N(R)C} 2PdX2] with these chelating N-heterocyclic carbene ligands is reported. Structural proofs of complexes 28 and 46 are represented by X-ray diffraction studies. Catalytic applications in the Mizoroki-Heck reaction are presented. Georg Thieme Verlag Stuttgart.

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