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87587-77-7

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87587-77-7 Usage

Components

1-ethyl-3-methylimidazolium chloride and aluminum chloride
The kit includes these reagents, which react to form the ionic liquid.

Type of ionic liquid

1-ethyl-3-methylimidazolium cations and chloroaluminate anions
Consisting of these charged species, the ionic liquid is formed.

Applications

Organic synthesis, electrochemistry, and biotechnology
The ionic liquid is commonly used as a catalyst or solvent in these fields.

Properties

Non-volatility
The ionic liquid does not easily vaporize or evaporate, making it suitable for use in various chemical processes.

Properties

Thermal stability
The ionic liquid can withstand high temperatures without decomposing, allowing for its use in a range of applications.

Properties

High ionic conductivity
The ionic liquid allows for the efficient movement of ions, making it useful in electrochemical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 87587-77-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,5,8 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 87587-77:
(7*8)+(6*7)+(5*5)+(4*8)+(3*7)+(2*7)+(1*7)=197
197 % 10 = 7
So 87587-77-7 is a valid CAS Registry Number.

87587-77-7SDS

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 1-ethyl-3-methyl-2H-imidazole

1.2 Other means of identification

Product number -
Other names EMIM[Al2Cl7]

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:87587-77-7 SDS

87587-77-7Downstream Products

87587-77-7Relevant articles and documents

Liquid coordination complexes: A new class of Lewis acids as safer alternatives to BF3 in synthesis of polyalphaolefins

Hogg, James M.,Coleman, Fergal,Ferrer-Ugalde, Albert,Atkins, Martin P.,Swad?ba-Kwas?ny, Ma?gorzata

, p. 1831 - 1841 (2015)

Liquid coordination complexes (LCCs) are a new class of liquid Lewis acids, prepared by combining an excess of a metal halide (e.g. GaCl3) with a basic donor molecule (e.g. amides, amines or phosphines). LCCs were used to catalyse oligomerisation of 1-decene to polyalphaolefins (PAOs). Molecular weight distribution and physical properties of the produced oils were compliant with those required for low viscosity synthetic (Group IV) lubricant base oils. Kinematic viscosities at 100 °C of ca. 4 or 6 cSt were obtained, along with viscosity indexes above 120 and pour points below-57 °C. In industry, to achieve similar properties, BF3 gas is used as a catalyst. LCCs are proposed as a safer and economically attractive alternative to BF3 gas for the production of polyalphaolefins. This journal is

Synthesis of adamantane by ionic liquid-promoted isomerization of tricyclo[5.2.1.02,6]decane and H2SO4-mediated hydroisomerization of pentacyclo[4.4.0.02,4.03,7.08,10]decane

Aminov,Ramazanov,Khusnutdinov

, p. 102 - 106 (2022/02/17)

Adamantane was synthesized by skeletal isomerization of endo- and exo-tricyclo[5.2.1.02,6]-decanes in the presence of ionic liquid [Et3NH]+[Al2Cl7]?—CuSO4. A new method to synthesize adamantane in 75% yield by H2SO4-mediated hydroisomerization of its new precursor, pentacyclo[4.4.0.02,4.03,7.08,10]decane, was developed.

PROCESS FOR THE PREPARATION OF M-SUBSTITUTED ALKYLTOLUENES BY ISOMERIZATION WITH IONIC LIQUIDS AS CATALYSTS

-

Page/Page column 3, (2011/08/22)

The invention relates to a process for the preparation of m-substituted alkyltoluenes of the formula (I) in which R1 is C1-C5-alkyl, wherein a p-substituted alkyltoluene of the formula (II) in which R1 has the meaning given under formula (I), is isomerized in the presence of ionic liquids to give an m-substituted alkyltoluene of the formula (I). The m-substituted alkyltoluenes obtainable according to the invention are starting compounds for the preparation of fragrances and aroma substances.

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