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

104290-55-3

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104290-55-3 Usage

General Description

1H-Imidazole, 1-methyl-, monobenzoate is a chemical compound with the molecular formula C10H10N2O2. It is a derivative of 1-methylimidazole that is in the form of a monobenzoate salt. 1H-Imidazole, 1-methyl-, monobenzoate is often used as a building block in the synthesis of pharmaceutical drugs and other organic compounds. It has been found to possess antifungal and antibacterial properties, and as a result, it has potential applications in the development of new medications. Additionally, 1H-Imidazole, 1-methyl-, monobenzoate is used in the synthesis of conjugated polymers and other materials with electronic and optical properties. Overall, 1H-Imidazole, 1-methyl-, monobenzoate has diverse applications in the fields of medicine, materials science, and organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 104290-55-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,2,9 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 104290-55:
(8*1)+(7*0)+(6*4)+(5*2)+(4*9)+(3*0)+(2*5)+(1*5)=93
93 % 10 = 3
So 104290-55-3 is a valid CAS Registry Number.

104290-55-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name benzoic acid,1-methylimidazole

1.2 Other means of identification

Product number -
Other names 1H-Imidazole,1-methyl-,monobenzoate

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:104290-55-3 SDS

104290-55-3Downstream Products

104290-55-3Relevant academic research and scientific papers

METHODS OF RING OPENING POLYMERIZATION AND CATALYSTS THEREFOR

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Page/Page column 15, (2012/03/10)

A salt catalyst comprises an ionic complex of i) a nitrogen base comprising one or more guanidine and/or amidine functional groups, and ii) an oxoacid comprising one or more active acid groups, the active acid groups independently comprising a carbonyl group (C═O), sulfoxide group (S═O), and/or a phosphonyl group (P═O) bonded to one or more active hydroxy groups; wherein a ratio of moles of the active hydroxy groups to moles of the guanidine and/or amidine functional groups is greater than 0 and less than 2.0. The salt catalysts are capable of catalyzing ring opening polymerization of cyclic carbonyl compounds.

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