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METHYL 6-NITRO-1,2-BENZISOXAZOLE-3-CARBOXYLATE is an organic chemical compound with a complex structure that belongs to the class of organic compounds known as benzisoxazoles. It is characterized by its molecular formula C9H6N2O5 and is known to appear as a light yellowish powder or crystal. As an aromatic compound, its molecular structure includes a benzene ring, a nitrogen-oxygen (NO2) group, and a carboxylate functional group. Due to its reactivity, it must be handled with care under controlled conditions to prevent any inadvertent reactions.

5453-86-1

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5453-86-1 Usage

Uses

Used in Chemical Research:
METHYL 6-NITRO-1,2-BENZISOXAZOLE-3-CARBOXYLATE is used as a research compound for studying its chemical properties and potential applications in various fields.
Used in Industrial Applications:
METHYL 6-NITRO-1,2-BENZISOXAZOLE-3-CARBOXYLATE is used as an intermediate in certain chemical reactions, contributing to the synthesis of more complex molecules and compounds.
Used in Pharmaceutical Industry:
METHYL 6-NITRO-1,2-BENZISOXAZOLE-3-CARBOXYLATE is used as a building block in the development of new pharmaceutical compounds, potentially leading to the creation of novel drugs with various therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 5453-86-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,5 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5453-86:
(6*5)+(5*4)+(4*5)+(3*3)+(2*8)+(1*6)=101
101 % 10 = 1
So 5453-86-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H6N2O5/c1-15-9(12)8-6-3-2-5(11(13)14)4-7(6)16-10-8/h2-4H,1H3

5453-86-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 6-nitro-1,2-benzoxazole-3-carboxylate

1.2 Other means of identification

Product number -
Other names methyl 6-nitro-1,2-benzisoxazole-3-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:5453-86-1 SDS

5453-86-1Relevant academic research and scientific papers

Supramolecular kinetic effects by pillararenes: The synergism between spatiotemporal and preorganization concepts in decarboxylation reactions

Vieira Silveira, Eduardo,Montecinos, Rodrigo,Scorsin, Leandro,Garcia-Rio, Luis,Medeiros, Michelle,Nascimento, Vanessa,Nome, Faruk,Affeldt, Ricardo F.,Micke, Gustavo A.

, p. 6486 - 6494 (2021/04/16)

A study about spontaneous decarboxylation reactions of 3-carboxy-1,2-benzisoxazole (CBI) nitrated derivatives (6-NitroCBI and 5,6-DinitroCBI) compared with supramolecular kinetic effects promoted by two cationic pillararenes (P5A and P6A) has been carried

Synthesis and binding affinities of a series of 1,2-benzisoxazole-3-carboxamides to dopamine and serotonin receptors

Nuhrich,Varache-Lembege,Vercauteren,Dokhan,Renard,Devaux

, p. 957 - 964 (2007/10/03)

A series of 1,2-benzisoxazole-3-carboxamides derived from tertiary cycloalkylamines was synthesized and evaluated for affinity for serotonergic (5-HT3 and 5-HT4) and dopaminergic (D2) receptors using radioligand binding as

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