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1,2,4-Thiadiazol-3(2H)-one, 5-(4-chlorophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75444-53-0

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75444-53-0 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 8 carbon atoms, 5 hydrogen atoms, 1 chlorine atom, 2 nitrogen atoms, 1 oxygen atom, and 1 sulfur atom.

Explanation

Heterocyclic compounds are organic compounds containing a ring of atoms with at least one heteroatom, which is an atom other than carbon. In this case, the compound has a five-membered ring with two nitrogen atoms, one sulfur atom, and one oxygen atom.

Explanation

The compound has a ring structure consisting of five atoms, which is common in heterocyclic compounds.

Explanation

The compound has been studied for its potential to inhibit the growth of fungi and bacteria, making it a candidate for use in pharmaceuticals to treat infections.

Explanation

Due to its potential therapeutic properties, the compound may be used in the development of treatments for a range of diseases, although specific applications have not been mentioned in the provided material.

Explanation

The compound can be used as a starting material or intermediate in the synthesis of other organic compounds, which may have various applications in the pharmaceutical, chemical, or materials science industries.

Explanation

The compound is commonly used in pharmaceutical research and development due to its potential therapeutic properties and applications in the treatment of various diseases.

Class

Heterocyclic organic compounds

Structure

Five-membered ring

Therapeutic properties

Potential antifungal and antibacterial agent

Application

Treatment of various diseases

Use as an intermediate

Synthesis of other organic compounds

Research and development

Pharmaceutical industry

Check Digit Verification of cas no

The CAS Registry Mumber 75444-53-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,4,4 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 75444-53:
(7*7)+(6*5)+(5*4)+(4*4)+(3*4)+(2*5)+(1*3)=140
140 % 10 = 0
So 75444-53-0 is a valid CAS Registry Number.

75444-53-0Downstream Products

75444-53-0Relevant academic research and scientific papers

Reactions of Trimethylsilyl Azide with Heterocumulenes

Tsuge, Otohiko,Urano, Satoshi,Oe, Koji

, p. 5130 - 5136 (2007/10/02)

Trimethylsilyl azide (TMSA) reacted with aryl isocyanates to give arylcarbamoyl azides, 1-aryl-5(4H)-tetrazolinones, and / or 1-aryl-4-(arylcarbamoyl)-5(4H)-tetrazolinones, whose yields were dependent on the reaction conditions.The reaction between TMSA and benzoyl or thiobenzoyl isocyanates provides a facile method for the preparation of 5-aryl-3-hydroxy-1,2,4-oxadiazoles or -1,2,4-thiadiazoles, respectively.However, with phenyl or benzoyl isothiocyanate, 1-anilino-1,2,3,4-thiatriazole or benzoylcyanamide was obtained in low yield, respectively.TMSA reacted with carbodiimides to afford the corresponding 5-aminotetrazoles.Tetraphenylsuccinimide, N-(diphenylacetyl)tetraphenylsuccinimide, 1,3-bis(diphenylmethyl)urea, and / or benziloylamide were obtained from the reaction of TMSA with diphenyl ketene.The pathways for the formation of the above products are also described.

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