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2-Sulfanyl-N'-(sulfanylacetyl)acetohydrazide is a hydrazide derivative characterized by its molecular formula C4H10N2O2S3. It features an acetylacetohydrazide core with two thiol (sulfhydryl) groups attached, which endows it with unique structural and functional properties. This chemical compound holds potential in the realm of medicinal chemistry, particularly for the development of pharmaceuticals and biologically active molecules. The versatility of its thiol groups makes it a valuable compound for organic synthesis and chemical reactions, attracting interest for further study and potential applications across various scientific and industrial fields.

62-48-6

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62-48-6 Usage

Uses

Used in Medicinal Chemistry:
2-Sulfanyl-N'-(sulfanylacetyl)acetohydrazide is used as a building block in the synthesis of pharmaceuticals for its ability to form stable complexes with metal ions and participate in various chemical reactions due to its thiol groups.
Used in Organic Synthesis:
In the field of organic synthesis, 2-Sulfanyl-N'-(sulfanylacetyl)acetohydrazide is used as a versatile intermediate for the creation of a wide range of biologically active molecules, leveraging its reactivity and the potential for forming covalent bonds with other molecules.
Used in Chemical Reactions:
2-Sulfanyl-N'-(sulfanylacetyl)acetohydrazide is utilized as a reactant in various chemical reactions, taking advantage of the nucleophilic properties of its thiol groups to form new compounds with desired properties.
Used in Drug Development:
In the pharmaceutical industry, 2-Sulfanyl-N'-(sulfanylacetyl)acetohydrazide is used as a precursor in the development of new drugs, particularly those targeting metalloenzymes or requiring the formation of disulfide bonds for stability and activity.
Used in Biochemical Research:
2-Sulfanyl-N'-(sulfanylacetyl)acetohydrazide serves as a research tool in biochemical studies, where its interaction with proteins and other biomolecules can provide insights into the mechanisms of action and potential therapeutic applications.
Each of these applications highlights the diverse utility of 2-Sulfanyl-N'-(sulfanylacetyl)acetohydrazide, underpinned by its unique chemical structure and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 62-48-6 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 6 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 62-48:
(4*6)+(3*2)+(2*4)+(1*8)=46
46 % 10 = 6
So 62-48-6 is a valid CAS Registry Number.

62-48-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-sulfanyl-N'-(2-sulfanylacetyl)acetohydrazide

1.2 Other means of identification

Product number -
Other names Acetic acid, mercapto-, 2-(mercaptoacetyl)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:62-48-6 SDS

62-48-6Upstream product

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