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518052-13-6

1-(hydroxymethyl)-1-[(5-nitro-2-furyl)methyleneamino]urea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 518052-13-6 Structure

  • Basic information

    1. Product Name: 1-(hydroxymethyl)-1-[(5-nitro-2-furyl)methyleneamino]urea
    2. Synonyms:
    3. CAS NO:518052-13-6
    4. Molecular Formula: C7H8N4O5
    5. Molecular Weight: 228.16
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 518052-13-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 433.9°C at 760 mmHg
    3. Flash Point: 216.2°C
    4. Appearance: N/A
    5. Density: 1.68g/cm3
    6. Vapor Pressure: 2.69E-08mmHg at 25°C
    7. Refractive Index: 1.658
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1-(hydroxymethyl)-1-[(5-nitro-2-furyl)methyleneamino]urea(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-(hydroxymethyl)-1-[(5-nitro-2-furyl)methyleneamino]urea(518052-13-6)
    12. EPA Substance Registry System: 1-(hydroxymethyl)-1-[(5-nitro-2-furyl)methyleneamino]urea(518052-13-6)

  • 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: 518052-13-6(Hazardous Substances Data)

518052-13-6 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.
2. Urea derivative

Explanation

It is a compound derived from urea, which is an organic compound with the chemical formula (NH2)2CO.
3. Contains a nitrofuran group

Explanation

The compound has a nitrofuran functional group, which is a furan ring with a nitro group (-NO2) attached to it.
4. Potential pharmacological properties

Explanation

The compound has been studied for its possible therapeutic effects, which include antibacterial and antitumor activities.
5. Antibacterial activity

Explanation

The compound may have the ability to inhibit the growth of or kill bacteria, making it potentially useful in the treatment of bacterial infections.
6. Antitumor activity

Explanation

The compound may exhibit properties that help in the prevention or treatment of tumors, making it a potential candidate for cancer therapy.
7. Research use as a building block

Explanation

It has been used in the synthesis of novel compounds with potential therapeutic applications, serving as a starting point for creating new molecules with desired properties.
8. Unique structure

Explanation

The compound's structure is of interest in the field of medicinal chemistry due to its potential for further investigation and development of new therapeutic agents.
9. Interest in medicinal chemistry

Explanation

The compound's properties and structure make it a promising target for research in the development of new drugs and therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 518052-13-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,8,0,5 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 518052-13:
(8*5)+(7*1)+(6*8)+(5*0)+(4*5)+(3*2)+(2*1)+(1*3)=126
126 % 10 = 6
So 518052-13-6 is a valid CAS Registry Number.

518052-13-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Hydroxymethylnitrofurazone

1.2 Other means of identification

Product number -
Other names N-hydroxymethylnitrofurazone

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:518052-13-6 SDS

518052-13-6Downstream Products

518052-13-6Relevant articles and documents

Synthesis optimization of hydroxymethylnitrofurazone, an antichagasi candidate, using 32 factorial design

Trossini, Gustavo H.G.,Giarolla, Jeanine,De Rezende, Leandro,Do Amaral, Antonia T.,Zaim, Marcio H.,Bruns, Roy E.,Ferreira, Elizabeth I.

experimental part, p. 191 - 195 (2011/07/08)

Hydroxymethylnitrofurazone presents in vitro activity against Trypanosoma cruzi. The optimization of the synthesis of this compound was performed through a 32 factorial statistical design. Quadratic model produced the best response surface predicting a maximum yield (82%) close to the center design point with a seven hours reaction and a 1:1.5 (NF:K2CO3) ratio.

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