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5446-32-2

2-amino-4-(diethylsulfamoyl)butanoic acid is a chemical compound with the molecular formula C8H18N2O4S. It is an amino acid derivative featuring a diethylsulfamoyl group attached to the 4-position of a butanoic acid backbone. 2-amino-4-(diethylsulfamoyl)butanoic acid is known for its potential applications in pharmaceuticals, particularly as a building block for the synthesis of various drug molecules. Its structure allows for the formation of salts and derivatives, which can be further modified to create compounds with specific therapeutic properties. The compound's unique combination of functional groups, including the amino group, carboxylic acid, and sulfamoyl group, makes it a versatile intermediate in organic synthesis and medicinal chemistry.

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  • 5446-32-2 Structure

  • Basic information

    1. Product Name: 2-amino-4-(diethylsulfamoyl)butanoic acid
    2. Synonyms:
    3. CAS NO:5446-32-2
    4. Molecular Formula: C8H18N2O4S
    5. Molecular Weight: 238.3045
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 5446-32-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 408.2°C at 760 mmHg
    3. Flash Point: 200.6°C
    4. Appearance: N/A
    5. Density: 1.27g/cm3
    6. Vapor Pressure: 8.35E-08mmHg at 25°C
    7. Refractive Index: 1.52
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-amino-4-(diethylsulfamoyl)butanoic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-amino-4-(diethylsulfamoyl)butanoic acid(5446-32-2)
    12. EPA Substance Registry System: 2-amino-4-(diethylsulfamoyl)butanoic acid(5446-32-2)

  • 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: 5446-32-2(Hazardous Substances Data)

5446-32-2 Usage

General Description

2-amino-4-(diethylsulfamoyl)butanoic acid is a chemical compound with the molecular formula C10H21N3O4S. It is a derivative of butanoic acid and contains both an amino group and a sulfamoyl group. 2-amino-4-(diethylsulfamoyl)butanoic acid is commonly used as a diuretic and can aid in the treatment of edema and other conditions related to fluid retention. It works by inhibiting the reabsorption of sodium and chloride ions in the kidneys, leading to increased urine production. Additionally, it is also utilized in the research and development of pharmaceuticals and other industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 5446-32-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,4 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5446-32:
(6*5)+(5*4)+(4*4)+(3*6)+(2*3)+(1*2)=92
92 % 10 = 2
So 5446-32-2 is a valid CAS Registry Number.

5446-32-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-4-(diethylsulfamoyl)butanoic acid

1.2 Other means of identification

Product number -
Other names -

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:5446-32-2 SDS

5446-32-2Downstream Products

5446-32-2Relevant articles and documents

Investigation of mechanism of nitrogen transfer in glucosamine 6- phosphate synthase with the use of transition state analogs

Milewski, SlLawomir,Hoffmann, Maria,Andruszkiewicz, Ryszard,Borowski, Edward

, p. 283 - 296 (2007/10/03)

Several structural analogs of putative tetrahedral intermediates of the reaction catalyzed by the glutamine amide transfer domain of Candida albicans glucosamine 6-phosphate synthase have been designed and synthesized. Esters and amides of γ-phosphonic and γ-sulfonic analogs of glutamine and glutamic acid were tested as potential inhibitors of the enzyme. N-substituted amides 9 and 15 were found to be the strongest inhibitors in the series. Structure- activity relationship studies led to conclusions supporting the possibility of a direct nucleophilic attack of the glutamine amide nitrogen on an electrophilic site of the enzyme-bound fructose 6-phosphate as the most likely mechanism of nitrogen transfer in glucosamine 6-phosphate synthase.

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