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121347-31-7

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121347-31-7 Usage

Description

1-(2,5-Dimethoxyphenyl)-2-oximino-1-propanone is a chemical compound with the molecular formula C12H17NO3. It belongs to the class of oximino ketones and contains a phenyl ring with two methoxy groups and an oximino group attached to a propanone backbone. 1-(2,5-Dimethoxyphenyl)-2-oximino-1-propanone is known for its potential use in the synthesis of various organic compounds and pharmaceuticals. It has been studied for its pharmacological properties and has shown promising potential as an antifungal and antibacterial agent. Additionally, it may also have applications in drug discovery and development as a building block for more complex chemical compounds.

Uses

Used in Pharmaceutical Industry:
1-(2,5-Dimethoxyphenyl)-2-oximino-1-propanone is used as an intermediate for the synthesis of various pharmaceuticals due to its unique chemical structure and potential pharmacological properties.
Used in Organic Synthesis:
1-(2,5-Dimethoxyphenyl)-2-oximino-1-propanone is used as a building block for the synthesis of more complex chemical compounds, contributing to the development of new materials and products.
Used in Antifungal Applications:
1-(2,5-Dimethoxyphenyl)-2-oximino-1-propanone is used as an antifungal agent for its potential to combat fungal infections, providing a valuable alternative in the treatment of various fungal diseases.
Used in Antibacterial Applications:
1-(2,5-Dimethoxyphenyl)-2-oximino-1-propanone is used as an antibacterial agent for its potential to fight bacterial infections, offering a promising option in the development of new antibiotics to combat drug-resistant bacteria.
Used in Drug Discovery and Development:
1-(2,5-Dimethoxyphenyl)-2-oximino-1-propanone is used as a starting material in drug discovery and development, with its unique structure and properties making it a valuable candidate for the creation of new therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 121347-31-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,3,4 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 121347-31:
(8*1)+(7*2)+(6*1)+(5*3)+(4*4)+(3*7)+(2*3)+(1*1)=87
87 % 10 = 7
So 121347-31-7 is a valid CAS Registry Number.

121347-31-7SDS

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 1-(2,5-dimethoxyphenyl)-2-hydroxyiminopropan-1-one

1.2 Other means of identification

Product number -
Other names 2-Hydroxyimino-1-(2.5-dimethoxy-phenyl)-propanon-(1)

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:121347-31-7 SDS

121347-31-7Relevant articles and documents

Preparation method of methoxamine hydrochloride degradation impurities

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Paragraph 0014; 0026-0027, (2021/05/08)

The invention discloses a preparation method of a methoxamine hydrochloride degradation impurity, and the method comprises the following steps: 1, adding a methoxamine hydrochloride impurity into a reaction flask, and adding a hydrolysis reagent, an alkylation reagent, a protective agent, a deprotection reagent and a nitric acid reagent; 2, performing reacting at 40-60 DEG C for 1-3 hours, and adding 100ml of extracting agent for extracting; 3, carrying out the organic layer concentration drying and column chromatography, and obtaining the treated impurities. According to the preparation method, 2-hydroxy-5-methoxyacetone is taken as a raw material and is subjected to multiple process treatments of alkylation, acylation, oximation and hydrolysis, so that the stability of an intermediate of the obtained methoxamine hydrochloride is improved, and impurities of the methoxamine hydrochloride can be degraded.

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