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5-Isoxazolecarboxaldehyde,3-methyl-4-nitro-(7CI,8CI,9CI) is a heterocyclic chemical compound with the molecular formula C6H5N3O3. It features an isoxazole ring, which is a five-membered ring containing both nitrogen and oxygen atoms, along with a methyl and a nitro group attached to the ring. 5-Isoxazolecarboxaldehyde,3-methyl-4-nitro-(7CI,8CI,9CI) serves as a versatile intermediate in the synthesis of various chemical products.

6436-64-2

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6436-64-2 Usage

Uses

Used in Pharmaceutical Industry:
5-Isoxazolecarboxaldehyde,3-methyl-4-nitro-(7CI,8CI,9CI) is used as a synthetic intermediate for the development of pharmaceuticals. Its unique structure allows it to be a key component in the creation of new drugs, potentially contributing to the treatment of various medical conditions.
Used in Agrochemical Industry:
In the agrochemical sector, 5-Isoxazolecarboxaldehyde,3-methyl-4-nitro-(7CI,8CI,9CI) is utilized as an intermediate in the synthesis of pesticides and other agrochemicals. Its incorporation can enhance the effectiveness of these products in protecting crops and managing pests.
Used in Dye Production:
5-Isoxazolecarboxaldehyde,3-methyl-4-nitro-(7CI,8CI,9CI) is also used in the production of organic dyes. Its chemical properties make it suitable for creating a range of colors used in various industries, including textiles and printing.
Used in Research and Development:
5-Isoxazolecarboxaldehyde,3-methyl-4-nitro-(7CI,8CI,9CI) holds potential for research and development in the fields of chemistry and pharmacology. It can be employed in experimental procedures to explore new reactions, syntheses, and the discovery of novel chemical entities with potential applications in medicine and other areas.
Used in Fine Chemicals Production:
5-Isoxazolecarboxaldehyde,3-methyl-4-nitro-(7CI,8CI,9CI) is utilized in the manufacturing of fine chemicals, which are high-purity chemicals used in various specialized applications, such as in the fragrance, flavor, and cosmetics industries. Its unique structure and properties make it valuable in these high-specification chemical syntheses.

Check Digit Verification of cas no

The CAS Registry Mumber 6436-64-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,3 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6436-64:
(6*6)+(5*4)+(4*3)+(3*6)+(2*6)+(1*4)=102
102 % 10 = 2
So 6436-64-2 is a valid CAS Registry Number.

6436-64-2SDS

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 3-Methyl-4-nitroisoxazole-5-carbaldehyde

1.2 Other means of identification

Product number -
Other names 3-methyl-4-nitro-1,2-oxazole-5-carbaldehyde

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:6436-64-2 SDS

6436-64-2Downstream Products

6436-64-2Relevant academic research and scientific papers

A MILD METHOD FOR THE CONVERSION OF ACTIVATED ARYL METHYL GROUPS TO CARBOXALDEHYDES VIA THE UNCATALYZED PERIODATE CLEAVAGE OF ANAMINES

Vetelino, Michael G.,Coe, Jotham W.

, p. 219 - 222 (2007/10/02)

A mild procedure for the oxidative cleavage of aryl enamines to aryl aldehydes by periodate without the need for transition metal catalysis is presented.

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