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122222-10-0

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122222-10-0 Usage

Molecular weight

192.22 g/mol

Structure

A five-membered imidazole ring with a carboxylic acid group at position 5, two methyl groups at positions 1 and 2, and a methyl ester group attached to the carboxylic acid.

Appearance

White or off-white crystalline solid

Solubility

Slightly soluble in water, soluble in common organic solvents such as ethanol, methanol, and acetone.

Stability

Stable under normal temperature and pressure, but may decompose upon exposure to high temperatures or strong acids and bases.

Uses

Synthesis of pharmaceuticals and organic compounds, production of pesticides and herbicides, potential applications in medicinal chemistry for drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 122222-10-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,2,2 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 122222-10:
(8*1)+(7*2)+(6*2)+(5*2)+(4*2)+(3*2)+(2*1)+(1*0)=60
60 % 10 = 0
So 122222-10-0 is a valid CAS Registry Number.

122222-10-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2,3-dimethylimidazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names methyl 1,2-dimethylimidazole-5-carboxylate

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:122222-10-0 SDS

122222-10-0Upstream product

122222-10-0Downstream Products

122222-10-0Relevant articles and documents

Preparation of 1-alkylimidazoles

-

, (2008/06/13)

Process for the preparation of 1-alkylimidazoles of the general formula (I) STR1 where R1 is alkyl, R2 and R3 are hydrogen, alkyl, aryl, arylalkyl, or alkylaryl, R4 is carboxy, alkoxycarbonyl R5 OCC--, carbamoyl, or cyano, and R5 is an alkyl of from 1 to 8 carbon atoms--by the reaction of imidazoles of the general formula (II) STR2 with dialkyl sulfates of the general formula (III) at elevated temperatures in the presence of a carboxylic acid or anhydride or of both acid and anhydride.

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