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4-METHYL-OXAZOLE-5-CARBOXYLIC ACID AMIDE, also known as 4-methyl-5-oxazolcarboxamide, is a white solid chemical compound with the molecular formula C5H6N2O2. It is widely used in the pharmaceutical and agrochemical industries as a building block in the synthesis of organic compounds. This versatile compound has been studied for its potential biological activities, such as anticonvulsant and anti-inflammatory properties, making it an important chemical with a range of applications.

4866-00-6

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4866-00-6 Usage

Uses

Used in Pharmaceutical Industry:
4-METHYL-OXAZOLE-5-CARBOXYLIC ACID AMIDE is used as a building block for the synthesis of various organic compounds, contributing to the development of new pharmaceutical products. Its potential biological activities, such as anticonvulsant and anti-inflammatory properties, make it a valuable component in the formulation of medications for treating various health conditions.
Used in Agrochemical Industry:
In the agrochemical industry, 4-METHYL-OXAZOLE-5-CARBOXYLIC ACID AMIDE is utilized as a key component in the synthesis of agrochemicals, including pesticides and herbicides. Its versatility and potential biological activities contribute to the development of effective and environmentally friendly solutions for agricultural applications.
Overall, 4-METHYL-OXAZOLE-5-CARBOXYLIC ACID AMIDE is a crucial chemical compound with diverse applications in both the pharmaceutical and agrochemical industries, offering potential benefits in the development of new products and formulations.

Check Digit Verification of cas no

The CAS Registry Mumber 4866-00-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,6 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4866-00:
(6*4)+(5*8)+(4*6)+(3*6)+(2*0)+(1*0)=106
106 % 10 = 6
So 4866-00-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H6N2O2/c1-3-4(5(6)8)9-2-7-3/h2H,1H3,(H2,6,8)

4866-00-6SDS

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 4-methyl-1,3-oxazole-5-carboxamide

1.2 Other means of identification

Product number -
Other names 4-methyl-oxazole-5-carboxamide

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:4866-00-6 SDS

4866-00-6Relevant academic research and scientific papers

PROCESS FOR SYNTHESIS OF 4-METHYLOXAZOLE-5-CARBOXAMIDE

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Page/Page column 6, (2013/11/18)

The present invention provides a novel process for synthesis of 4-methyl-oxazole-5- carboxamide (OXA) which comprises reacting a compound of formula (I) with a high concentration of aqueous ammonia: (I) Wherein R1 is H or C1-10 alkyl.

PROCESS FOR 4-METHYLOXAZOLE-5-CARBOXAMIDE

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Page/Page column 6, (2013/02/28)

A process for the preparation of 4-methyl-oxazole-5-carboxamide, an intermediate in the synthesis of pyridoxine, by reacting lower alkyl 4-methyl-oxazole-5-carboxy-late with a molar excess of anhydrous, liquid ammonia.

Process for the manufacture of 5-cyano-4-lower alkyl-oxazoles

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, (2008/06/13)

A process for the manufacture of a 5-cyano-4-lower alkyl-oxazole by the dehydration of a 5-carbamoyl-4-lower alkyl-oxazole is disclosed. The reaction is carried out by dehydrating the oxazole with silicon tetrachloride in the presence of an amine in an aprotic organic solvent. 5-Carbamoyl-4-methyl-oxazole may be dehydrated by the process in accordance with the invention to obtain 5-cyano-4-methyl-oxazole, which is a valuable intermediate in the synthesis of pyridoxine.

Production of pyridoxine intermediates from diketene

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, (2008/06/13)

A process for the preparation of oxazoles, particularly 4-lower alkyl-5-cyanooxazoles, from diketene is disclosed.

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