Welcome to LookChem.com Sign In|Join Free

CAS

  • or

10138-46-2

N-Ethylacetoacetamide, also known as N-Ethyl-3-oxobutanamide, is an organic compound commonly utilized as a reagent in the chemical and pharmaceutical industries. It is characterized by its amide functional group and ethyl substituent, which contribute to its reactivity and versatility in various chemical reactions.

10138-46-2 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 10138-46-2 Structure

  • Basic information

    1. Product Name: N-Ethylacetoacetamide
    2. Synonyms: N-Ethylacetoacetamide;Acetoacetyl ethanolamine;N-Ethylacetylacetamide;N-ethylaceoacetamine
    3. CAS NO:10138-46-2
    4. Molecular Formula: C6H11NO2
    5. Molecular Weight: 129.15704
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 10138-46-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 282.1°C at 760 mmHg
    3. Flash Point: 135.3°C
    4. Appearance: /
    5. Density: 0.988g/cm3
    6. Vapor Pressure: 0.00342mmHg at 25°C
    7. Refractive Index: 1.426
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: N-Ethylacetoacetamide(CAS DataBase Reference)
    11. NIST Chemistry Reference: N-Ethylacetoacetamide(10138-46-2)
    12. EPA Substance Registry System: N-Ethylacetoacetamide(10138-46-2)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 10138-46-2(Hazardous Substances Data)

10138-46-2 Usage

Uses

Used in Pharmaceutical Industry:
N-Ethylacetoacetamide is used as a reagent for the preparation of selective A3 Adenosine receptor antagonists. These antagonists are important in the development of drugs targeting various conditions, such as chronic obstructive pulmonary disease (COPD), asthma, and other inflammatory disorders. The compound's unique structure allows it to participate in the synthesis of these therapeutic agents, potentially leading to improved treatment options for patients.

Check Digit Verification of cas no

The CAS Registry Mumber 10138-46-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,3 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10138-46:
(7*1)+(6*0)+(5*1)+(4*3)+(3*8)+(2*4)+(1*6)=62
62 % 10 = 2
So 10138-46-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H11NO2/c1-3-7-6(9)4-5(2)8/h3-4H2,1-2H3,(H,7,9)

10138-46-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-ethyl-3-oxobutanamide

1.2 Other means of identification

Product number -
Other names Acetessigsaeure-aethylamid

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:10138-46-2 SDS

10138-46-2Relevant articles and documents

Facile eco-friendly synthesis of novel chromeno[4,3-b]pyridine-2,5-diones and evaluation of their antimicrobial and antioxidant properties

Jaggavarapu, Satyanarayana Reddy,Kamalakaran, Anand Solomon,Jalli, Ventkata Prasad,Gangisetty, Sravan Kumar,Ganesh, Munusswamy Ramanujam,Gaddamanugu, Gopikrishna

, p. 187 - 195 (2014/04/03)

Rapid and facileaccess to novel chromeno[4,3-b]pyridine-2,5-dione derivatives was achieved by a mild base catalysed reaction of 4-chloro-3-formylcoumarin and acetoacetamides in PEG-300 as recyclable solvent. The compounds were evaluated for their antimicrobial activities against 3 Gram-positive and 3 Gram-negative bacteria (Staphylococcus epidermis, Vibrio parahaemolyticus, Bacillus subtilis, Escherichia coli, Staphylococcus aureus and Klebsiella pneumonia) with Cefotaxime control. They were further subjected to antioxidant studies using DPPH test with ascorbic acid control. While compounds 5d and 5k showed promising broad spectrum antibacterial properties against all the evaluated bacteria, compound 5g exhibited good antioxidant properties. Indian Academy of Sciences.

Facile eco-friendly synthesis of novel chromeno[4,3-b]pyridine-2,5-diones and evaluation of their antimicrobial and antioxidant properties

Jaggavarapu, Satyanarayana Reddy,Kamalakaran, Anand Solomon,Jalli, Ventkata Prasad,Gangisetty, Sravan Kumar,Ganesh, Munusswamy Ramanujam,Gaddamanugu, Gopikrishna

, p. 187 - 195 (2016/02/26)

Rapid and facile access to novel chromeno[4,3-b]pyridine-2,5-dione derivatives was achieved by a mild base catalysed reaction of 4-chloro-3-formylcoumarin and acetoacetamides in PEG-300 as recyclable solvent. The compounds were evaluated for their antimicrobial activities against 3 Gram-positive and 3 Gram-negative bacteria (Staphylococcus epidermis, Vibrio parahaemolyticus, Bacillus subtilis, Escherichia coli, Staphylococcus aureus and Klebsiella pneumonia) with Cefotaxime control. They were further subjected to antioxidant studies using DPPH test with ascorbic acid control. While compounds 5d and 5k showed promising broad spectrum antibacterial properties against all the evaluated bacteria, compound 5g exhibited good antioxidant properties. [Figure not available: see fulltext.]

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 10138-46-2