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1,2,5-Thiadiazole-3-carboximidic acid, 4-amino, hydrazide is a complex organic compound with the chemical formula C2H4N6S. It is a derivative of 1,2,5-thiadiazole, a five-membered heterocyclic ring containing sulfur, nitrogen, and carbon atoms. The compound features an amidic acid group at the 3-position, an amino group at the 4-position, and a hydrazide group attached to the nitrogen atom. This molecule is known for its potential applications in pharmaceuticals and agrochemicals, particularly as a building block for the synthesis of various biologically active compounds. Its unique structure allows for the formation of diverse chemical entities, making it a valuable intermediate in the development of new drugs and pesticides.

7254-01-5

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7254-01-5 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 2 carbon (C), 4 hydrogen (H), 6 nitrogen (N), and 1 sulfur (S) atoms.

Explanation

This structure consists of a thiadiazole ring fused with a carboximidic acid group at position 3, an amino group at position 4, and a hydrazide group attached to the amino group.

Explanation

Due to its unique structure and versatile reactivity, 1,2,5-Thiadiazole-3-carboximidic acid, 4-amino-, hydrazide is used as a starting material for creating new drug molecules in the pharmaceutical industry.

Explanation

Studies have shown that 1,2,5-Thiadiazole-3-carboximidic acid, 4-amino-, hydrazide exhibits potential antibacterial and antifungal activities, making it a promising candidate for the development of treatments for infectious diseases.

Explanation

The compound's structure and reactivity allow for the creation of new bioactive molecules with potential therapeutic applications in medicine.

Explanation

As a chemically important compound, 1,2,5-Thiadiazole-3-carboximidic acid, 4-amino-, hydrazide serves as a key building block for the synthesis of various bioactive molecules with potential applications in the medical field.

Chemical Structure

1,2,5-Thiadiazole-3-carboximidic acid, 4-amino-, hydrazide

Pharmaceutical Industry Application

Building block for synthesis of potential drug candidates

Biological Activities

Antibacterial and antifungal properties

Potential Medicinal Applications

Development of novel bioactive molecules

Chemical Importance

Valuable precursor in the development of bioactive molecules

Check Digit Verification of cas no

The CAS Registry Mumber 7254-01-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,5 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7254-01:
(6*7)+(5*2)+(4*5)+(3*4)+(2*0)+(1*1)=85
85 % 10 = 5
So 7254-01-5 is a valid CAS Registry Number.
InChI:InChI=1/C3H6N6S/c4-2(7-6)1-3(5)9-10-8-1/h6H2,(H2,4,7)(H2,5,9)

7254-01-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N',4-diamino-1,2,5-thiadiazole-3-carboximidamide

1.2 Other means of identification

Product number -
Other names 1,2,5-Thiadiazole-3-carboximidic acid,4-amino-,hydrazide

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:7254-01-5 SDS

7254-01-5Upstream product

7254-01-5Downstream Products

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