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36432-31-2

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36432-31-2 Usage

Type of compound

Ionic liquid

Composition

Composed entirely of ions

Melting point

Low melting point

Common use

Catalyst in organic synthesis reactions

Preparation

Used in the preparation of other ionic liquids

Application

Studied for potential applications in electrochemistry

Property

Exhibits high ionic conductivity

Fields of interest

Materials science and pharmaceuticals

Reason for interest

Unique properties and versatility

Check Digit Verification of cas no

The CAS Registry Mumber 36432-31-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,4,3 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 36432-31:
(7*3)+(6*6)+(5*4)+(4*3)+(3*2)+(2*3)+(1*1)=102
102 % 10 = 2
So 36432-31-2 is a valid CAS Registry Number.

36432-31-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3-trimethylimidazol-1-ium,iodide

1.2 Other means of identification

Product number -
Other names 1,2,3-trimethylimidazolinium iodide

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:36432-31-2 SDS

36432-31-2Relevant articles and documents

Effect of methyl groups onto imidazolium cation ring on liquid crystallinity and ionic conductivity of amphiphilic ionic liquids

Mukai, Tomohiro,Yoshio, Masafumi,Kato, Takashi,Ohno, Hiroyuki

, p. 1630 - 1631 (2004)

Phase transition behavior of imidazolium dodecylsulfonate was considerably affected by the introduction of methyl groups onto the imidazolium cation ring. Methyl group on the 2-position eliminated the liquid crystallinity. That on the 4-position was effective to suppress the crystallization. Copyright

Twisted Push-Pull Alkenes Bearing Geminal Cyclicdiamino and Difluoroaryl Substituents

Kundu, Abhinanda,Chandra, Shubhadeep,Mandal, Debdeep,Neuman, Nicolás I.,Mahata, Alok,Anga, Srinivas,Rawat, Hemant,Pal, Sudip,Schulzke, Carola,Sarkar, Biprajit,Chandrasekhar, Vadapalli,Jana, Anukul

, p. 12683 - 12692 (2021/09/18)

The systematic combination of N-heterocyclic olefins (NHOs) with fluoroarenes resulted in twisted push-pull alkenes. These alkenes carry electron-donating cyclicdiamino substituents and two electron-withdrawing fluoroaryl substituents in the geminal posit

Synthesis of new hetero-arylidene-9(10H)-anthrone derivatives and their biological evaluation

Baptista, Pedro V.,Branco, Paula S.,Fernandes, Alexandra R.,Malta, Gabriela,Peixoto, Daniela,Roma-Rodrigues, Catarina,Ferreira, Luísa M.

, (2020/04/22)

New hetero-arylidene-9(10H)-anthrone derivatives (1) were synthesized from reaction of 1,2-dimethyl-3-alkyl imidazolium salts (2) and 9-anthracenecarboxaldehyde. Ion exchange of the anion with dioctyl sulfosuccinate and lithium bis(trifluoromethanesulfonyl)imide led to the preparation of other derivatives. The antiproliferative effect of the compounds was evaluated in human ovarian (A2780) and colorectal (HCT116) carcinoma cell lines and in normal primary human fibroblasts. Compound 1 presented an antiproliferative effect related to the imidazolium pattern of substitution with compounds having a decyl group at the R-position (1c and 3c) showing the highest cytotoxic activities in all cell lines independently of the counter ion. Compounds 1b and 1c internalize A2780 cancer cells via a passive or an active transport, respectively, inducing A2780 cell death via an extrinsic apoptosis (1b) or intrinsic apoptosis and oncosis (1c). The localization of both compounds in the cytoplasm coupled to the absence of reactive oxygen species (ROS) induction suggest that the mechanisms of toxicity might be different than those of other anthracyclines currently used in chemotherapy.

N-Heterocyclic olefins as efficient phase-transfer catalysts for base-promoted alkylation reactions

Blümel, Marcus,Crocker, Reece D.,Harper, Jason B.,Enders, Dieter,Nguyen, Thanh V.

supporting information, p. 7958 - 7961 (2016/07/06)

N-Heterocyclic olefins (NHOs) have very recently emerged as efficient promoters for several chemical reactions due to their strong Br?nsted/Lewis basicities. Here we report the novel application of NHOs as efficient phase-transfer organocatalysts for synt

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