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OXAZOLE, 4-(CHLOROMETHYL)-2-METHYL-, also known as 4-(chloromethyl)-2-methyl-oxazole, is a heterocyclic compound characterized by a five-membered ring containing both oxygen and nitrogen atoms. This versatile chemical intermediate is widely utilized in the synthesis of pharmaceuticals, agrochemicals, and dyes, and has been recognized for its antimicrobial and antifungal properties, which contribute to its potential in the development of new drugs and materials.

141399-53-3

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141399-53-3 Usage

Uses

Used in Pharmaceutical Industry:
OXAZOLE, 4-(CHLOROMETHYL)-2-METHYLis used as a chemical intermediate for the synthesis of various pharmaceuticals, leveraging its unique structure and reactivity to facilitate the development of new drugs with diverse therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, OXAZOLE, 4-(CHLOROMETHYL)-2-METHYLserves as a key intermediate in the production of agrochemicals, including pesticides and herbicides, due to its potential to enhance the effectiveness and selectivity of these compounds in controlling pests and unwanted plant growth.
Used in Dye Industry:
OXAZOLE, 4-(CHLOROMETHYL)-2-METHYLis utilized as a building block in the synthesis of dyes, contributing to the creation of a wide range of colorants used in various industries, such as textiles, plastics, and printing inks.
Used in Material and Additive Production:
This chemical is also employed in the production of various materials and additives, where its properties can be harnessed to improve the performance or characteristics of the final products.
Used in Antimicrobial and Antifungal Applications:
OXAZOLE, 4-(CHLOROMETHYL)-2-METHYLis used as an antimicrobial and antifungal agent in the development of new drugs, thanks to its inherent properties that can combat a variety of microbial pathogens, offering potential therapeutic benefits in treating infections.
It is crucial to handle OXAZOLE, 4-(CHLOROMETHYL)-2-METHYLwith care, as it can pose hazards if not used or stored properly, underscoring the importance of safety measures in its application across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 141399-53-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,3,9 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 141399-53:
(8*1)+(7*4)+(6*1)+(5*3)+(4*9)+(3*9)+(2*5)+(1*3)=133
133 % 10 = 3
So 141399-53-3 is a valid CAS Registry Number.

141399-53-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(Chloromethyl)-2-methyl-1,3-oxazole

1.2 Other means of identification

Product number -
Other names 4-(CHLOROMETHYL)-2-METHYLOXAZOLE

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:141399-53-3 SDS

141399-53-3Relevant academic research and scientific papers

SUBSTITUTED OXOPYRIDINE DERIVATIVES

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Paragraph 0958-0961, (2017/11/07)

The invention relates to substituted oxopyridine derivatives and to processes for preparation thereof, and also to the use thereof for production of medicaments for treatment and/or prophylaxis of diseases, especially of cardiovascular disorders, preferably thrombotic or thromboembolic disorders, and oedemas, and also ophthalmic disorders.

SUBSTITUTED OXOPYRIDINE DERIVATIVES

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Paragraph 0830; 0831; 0832; 0833, (2017/10/27)

The invention relates to substituted oxopyridine derivatives and to processes for preparation thereof, and also to the use thereof for production of medicaments for treatment and/or prophylaxis of diseases, especially of cardiovascular disorders, preferably thrombotic or thromboembolic disorders, and oedemas, and also ophthalmic disorders.

SUBSTITUTED PYRIMIDINONE-PHENYL-PYRIMIDINYL COMPOUNDS

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Paragraph 0271, (2013/06/26)

The present disclosure provides pyrimidinone-phenyl-pyrimidinyl compounds useful in the treatment of p38 kinase mediated diseases, such as lymphoma and inflammatory disease, having the structure of Formula (I): wherein R1, R2, R3, R4 and R5 are as defined in the detailed description; pharmaceutical compositions comprising at least one of the compounds; and methods for treating p38 kinase mediated diseases using the compound.

OXADIAZOLE COMPOUNDS WHICH INHIBIT BETA-SECRETASE ACTIVITY AND METHODS OF USE THEREOF

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Page/Page column 84-85, (2012/05/05)

The invention provides novel beta-secretase inhibitors and methods for their including methods of treating Alzheimer's disease.

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