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1H-Imidazole-2-methanol, 1-methyl-, monohydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

718642-27-4

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718642-27-4 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

The structure refers to the arrangement of atoms in the compound, with the imidazole ring having a methyl group at the 1st position and a hydroxyl group at the 2nd position.

Explanation

Imidazole is a type of aromatic heterocycle, which means it has a ring structure with alternating single and double bonds and contains two nitrogen atoms that are not adjacent to each other.

Explanation

The addition of a hydrochloride group to the imidazole ring results in the formation of the monohydrochloride salt, which is the compound in question.

Explanation

1H-Imidazole-2-methanol, 1-methyl-, monohydrochloride serves as an intermediate in the production of various pharmaceutical drugs, meaning it is a precursor or building block in the synthesis process.

Explanation

The compound is used as a reagent in organic synthesis, which involves the formation or manipulation of carbon-containing compounds.

Explanation

The compound is also used in biochemical research, which focuses on the chemical processes and substances occurring within living organisms.

Explanation

Due to the presence of the hydroxyl and hydrochloride groups, the compound is soluble in water and other polar solvents.

Explanation

The compound is considered stable when stored and handled properly, meaning it does not readily decompose or react with other substances under typical conditions.

Explanation

The compound is typically found in a crystalline or solid form, which is a common state for many organic compounds.

Structure

1H-Imidazole-2-methanol, 1-methyl

Aromatic Heterocycle

Five-membered ring with two non-adjacent nitrogen atoms

Hydrochloride Salt

Contains a hydrochloride (HCl) group

Pharmaceutical Intermediate

Used in the synthesis of pharmaceutical drugs

Reagent in Organic Synthesis

Utilized in various organic reactions

Biochemical Research

Employed in biochemical studies

Solubility

Soluble in water and polar solvents

Stability

Relatively stable under normal conditions

Appearance

Crystalline or solid form

Check Digit Verification of cas no

The CAS Registry Mumber 718642-27-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,1,8,6,4 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 718642-27:
(8*7)+(7*1)+(6*8)+(5*6)+(4*4)+(3*2)+(2*2)+(1*7)=174
174 % 10 = 4
So 718642-27-4 is a valid CAS Registry Number.

718642-27-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxymethyl-1-methylimidazole hydrochloride

1.2 Other means of identification

Product number -
Other names N-methyl-2 -hydroxymethylimidazole hydrochloride

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:718642-27-4 SDS

718642-27-4Upstream product

718642-27-4Downstream Products

718642-27-4Relevant academic research and scientific papers

Substituted thiazoles as immunoregulants

-

, (2008/06/13)

Thiazole derivatives have been made, for example, by reacting a 2-aryl-2,2-dialkoxyethylamine with an appropriately substituted aryl acetyl halide followed by treating the resulting amide with diphosphoryl pentasulfide. The thiazole derivatives are found to be effective immunoregulants.

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