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24309-97-5

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24309-97-5 Usage

Description

N-(2-Hydroxyethyl)acetoacetamide is an organic compound that serves as an intermediate in the synthesis of various organic chemicals, such as quinoxaline derivatives. It is characterized by its yellow to brownish solidified melt appearance.

Uses

Used in Chemical Synthesis:
N-(2-Hydroxyethyl)acetoacetamide is used as an intermediate for the synthesis of different organic chemicals, including quinoxaline derivatives. Its role in the synthesis process is crucial for the production of these chemicals, which have various applications in the chemical industry.
Used in Pharmaceutical Industry:
N-(2-Hydroxyethyl)acetoacetamide is used as a building block in the development of pharmaceutical compounds. Its unique chemical structure allows it to be a valuable component in the creation of new drugs with potential therapeutic applications.
Used in Research and Development:
In the field of research and development, N-(2-Hydroxyethyl)acetoacetamide is utilized for studying the properties and reactions of organic compounds. It can be employed in various experiments to better understand the behavior of similar molecules and their potential uses in various industries.
Used in Dye and Pigment Industry:
N-(2-Hydroxyethyl)acetoacetamide can be used as a starting material for the production of dyes and pigments. Its chemical properties make it suitable for the synthesis of colorants that can be used in various applications, such as textiles, plastics, and printing inks.
Used in Cosmetics Industry:
In the cosmetics industry, N-(2-Hydroxyethyl)acetoacetamide may be used as an ingredient in the formulation of various cosmetic products. Its properties can contribute to the development of products with improved performance and enhanced benefits for the end user.

Check Digit Verification of cas no

The CAS Registry Mumber 24309-97-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,0 and 9 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 24309-97:
(7*2)+(6*4)+(5*3)+(4*0)+(3*9)+(2*9)+(1*7)=105
105 % 10 = 5
So 24309-97-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H11NO3/c1-5(9)4-6(10)7-2-3-8/h8H,2-4H2,1H3,(H,7,10)

24309-97-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-hydroxyethyl)acetoacetamide

1.2 Other means of identification

Product number -
Other names N-(2-Hydroxyethyl)acetoacetamid

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:24309-97-5 SDS

24309-97-5Relevant articles and documents

Fe(III) Complex Compounds For The Treatment And Prophylaxis Of Iron Deficiency Symptoms And Iron Deficiency Anemias

-

Paragraph 0394; 0395; 0396; 0397; 0398; 0399, (2013/05/09)

The invention relates to iron(III) complex compounds and pharmaceutical compositions comprising them for the use as medicaments, in particular for the treatment and/or prophylaxis of iron deficiency symptoms and iron deficiency anemias.

6-FLUORO-7-(1-PIPERAZINYL)QUINOXALINE 1,4-DIOXIDES. PART I. 2-(N-2-HYDROXYALKYLCARBAMOYL) DERIVATIVES

El-Abadelah, Mustafa M.,Nazer, Musa Z.,El-Abadla, Naser S.,Meier, Herbert

, p. 2203 - 2220 (2007/10/03)

A series of N--β-aminoalkanol 1,4-dioxides (12a-h) have been synthesized for bioassay via the Beirut reaction of 5(6)-fluoro-6(5)-(4-methyl-1-piperazinyl)benzofuroxan (9) with the appropriate N-acetoacetyl-β-aminoalkanol in the presence of triethylamine.Preliminary in vitro investigations have indicated that none of the title compounds exhibits any significant antibacterial potency at concentrations /= 200 μg/ml.

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