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3-(1,1-dioxido-2-phenyl-1,4,2-dithiazolidin-3-ylidene)-1,1-dimethylthiourea, also known as N,N’-dimethyl-N,N’-(3,3-dioxo-1,4,2-dithiazolidine-2,5-diylidene) dithiourea, is a chemical compound with the molecular formula C10H12N4O2S3. It is a thiourea derivative featuring a dithiazolidinone ring, which endows it with a range of biological activities and antimicrobial properties. 3-(1,1-dioxido-2-phenyl-1,4,2-dithiazolidin-3-ylidene)-1,1-dimethylthiourea holds promise in various fields, including pharmaceuticals and agrochemicals, due to its potential applications in treating diseases and as a preservative.

64803-02-7

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64803-02-7 Usage

Uses

Used in Pharmaceutical Applications:
3-(1,1-dioxido-2-phenyl-1,4,2-dithiazolidin-3-ylidene)-1,1-dimethylthiourea is used as a potential therapeutic agent for various diseases, including cancer, due to its antimicrobial and biological activities. It may contribute to the development of new drugs by targeting specific pathways or mechanisms involved in disease progression.
Used in Agrochemical Applications:
In the agrochemical industry, 3-(1,1-dioxido-2-phenyl-1,4,2-dithiazolidin-3-ylidene)-1,1-dimethylthiourea is used as an antifungal and antibacterial agent to protect crops from microbial infections, thereby enhancing crop yield and quality.
Used as a Reversible Inhibitor of Metalloproteinases:
3-(1,1-dioxido-2-phenyl-1,4,2-dithiazolidin-3-ylidene)-1,1-dimethylthiourea is used as a reversible inhibitor of metalloproteinases, which are enzymes involved in various physiological and pathological processes. Its inhibitory effect on these enzymes may have potential applications in the treatment of diseases where metalloproteinases play a crucial role.
Used as a Food Preservative:
3-(1,1-dioxido-2-phenyl-1,4,2-dithiazolidin-3-ylidene)-1,1-dimethylthiourea may be used as a food preservative to extend the shelf life of perishable food products by inhibiting the growth of spoilage-causing microorganisms.
Further research is necessary to fully understand the potential uses and effects of 3-(1,1-dioxido-2-phenyl-1,4,2-dithiazolidin-3-ylidene)-1,1-dimethylthiourea, ensuring its safe and effective application in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 64803-02-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,8,0 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 64803-02:
(7*6)+(6*4)+(5*8)+(4*0)+(3*3)+(2*0)+(1*2)=117
117 % 10 = 7
So 64803-02-7 is a valid CAS Registry Number.

64803-02-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (3E)-3-(1,1-dioxo-2-phenyl-1,4,2-dithiazolidin-3-ylidene)-1,1-dimethylthiourea

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:64803-02-7 SDS

64803-02-7Downstream Products

64803-02-7Relevant academic research and scientific papers

Sultam thioureas: Synthesis and antiviral activity against west nile virus

Feeny, Rachel M.,Le, Diane N.,Parks, Joseph W.,Epstein, Mark G.,Pagano, Joseph V.,Abbene, Albert C.,Graham, Elaina B.,Farrell, Joanna R.,McGuire, Jason R.,Zoellner, Robert W.,Valente, Edward J.,Barklis, Eric,Wood, Warren J. L.

experimental part, p. 301 - 305 (2012/03/08)

The syntheses of eleven sultam thioureas, including nine new compounds, are described. These compounds were synthesized from thioureas and include the first sultam thioureas in which the two thiourea nitrogen groups are not identical. In addition, the first X-ray crystal structures of sultam thioureas and the antiviral activity of these compounds against West Nile virus (WNV) are reported. Georg Thieme Verlag Stuttgart New York.

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