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1,3-Bis(1-adamantyl)-4,5-dihydroimidazolium chloride, min. 97%, is a high-purity imidazolium salt compound characterized by its chloride ion and 1,3-Bis(1-adamantyl)-4,5-dihydroimidazolium cation. With a molecular formula of C21H34ClN and a molecular weight of 339.94 g/mol, this chemical is renowned for its exceptional stability and catalytic efficiency in a range of organic synthesis processes, establishing its utility in the domain of organic chemistry.

871126-33-9

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871126-33-9 Usage

Uses

Used in Organic Synthesis:
1,3-Bis(1-adamantyl)-4,5-dihydroimidazolium chloride, min. 97% is utilized as a catalyst in various organic synthesis applications due to its high stability and efficiency in facilitating synthetic reactions. Its unique structure and properties allow it to effectively catalyze a wide array of chemical transformations, enhancing the yield and selectivity of the reactions it is involved in.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 1,3-Bis(1-adamantyl)-4,5-dihydroimidazolium chloride, min. 97% is employed as a catalyst for the synthesis of complex organic molecules, including those used in the development of new drugs. Its ability to accelerate reaction rates and improve product yields makes it a valuable asset in the production of pharmaceutical compounds.
Used in Chemical Research:
1,3-Bis(1-adamantyl)-4,5-dihydroimidazolium chloride, min. 97% is also used in academic and industrial research settings as a catalyst for exploring new synthetic pathways and developing innovative chemical processes. Its versatility and reliability in catalyzing reactions make it an essential tool for advancing the frontiers of chemical science.
Used in Material Science:
In the field of material science, 1,3-Bis(1-adamantyl)-4,5-dihydroimidazolium chloride, min. 97% is applied as a catalyst in the synthesis of novel materials with specific properties. Its role in facilitating the formation of these materials can lead to advancements in areas such as polymer chemistry, nanotechnology, and the development of new materials with tailored characteristics for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 871126-33-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,1,1,2 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 871126-33:
(8*8)+(7*7)+(6*1)+(5*1)+(4*2)+(3*6)+(2*3)+(1*3)=159
159 % 10 = 9
So 871126-33-9 is a valid CAS Registry Number.

871126-33-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-Imidazolium, 4,5-dihydro-1,3-bis(tricyclo[3.3.1.13,7]dec-1-yl)-, chloride

1.2 Other means of identification

Product number -
Other names 1,3-BIS(1-ADAMANTYL)-4,5-DIHYDROIMIDAZOLIUM CHLORIDE

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:871126-33-9 SDS

871126-33-9Downstream Products

871126-33-9Relevant academic research and scientific papers

1,3-bi-adamantane-4,5-glyoxalidine cuprous chloride salt and preparation method thereof

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, (2019/10/02)

The invention discloses 1,3-bi-adamantane-4,5-glyoxalidine cuprous chloride salt and a preparation method thereof. 1,3-bi-adamantane-4,5-glyoxalidine is dissolved in a THF solution; a certain quantity of potassium tert-butoxide is added as alkali; cuprous chloride is selected as a metal precursor; the metal precursor is slowly added; after the addition is completed, stirring is performed for more than 12h for preparing the 1,3-bi-adamantane-4,5-glyoxalidine cuprous chloride salt. Two side walls of the used ligand of glyoxalidine salt are adamantine alkyl groups with high electron donating capability and low polarity; the stability of ligand and metal complexation reaction and the lipid solubility of catalysts are favorably improved; the ligand and the metal generate a target product through simple symbiotic reaction; the preparation method is simple and convenient; the implementation is easy; the target product is applicable to aerobic oxidation reaction of alcohol; high yield can be obtained under the mild reaction conditions.

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