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1,3,4-Thiadiazol-2(3H)-one,5-amino-3-ethyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

211388-15-7

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211388-15-7 Usage

Explanation

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

Explanation

The compound belongs to the thiadiazole family, which is a group of five-membered heterocyclic compounds containing one sulfur and two nitrogen atoms.

Explanation

The compound has a five-membered ring structure with one sulfur and two nitrogen atoms, along with other carbon and hydrogen atoms.

Explanation

The compound is used as a building block or intermediate in the production of different pharmaceutical drugs due to its unique chemical properties.

Explanation

The compound is also used in the agricultural industry as an intermediate in the synthesis of various agrochemicals, such as pesticides and fertilizers.

Explanation

Research has been conducted to explore the compound's ability to reduce inflammation, which could lead to the development of new anti-inflammatory drugs.

Explanation

The compound has been investigated for its ability to inhibit bacterial growth, which could result in the development of new anti-bacterial treatments.

Explanation

Scientists continue to study the compound to better understand its properties and potential applications in various fields, including medicine and agriculture.

Family

Thiadiazole

Structure

Five-membered heterocyclic ring

Pharmaceutical Applications

Intermediate in the synthesis of various pharmaceutical drugs

Agricultural Applications

Intermediate in the synthesis of various agrochemicals

Anti-inflammatory Potential

Studied for its potential as an anti-inflammatory agent

Anti-bacterial Potential

Studied for its potential as an anti-bacterial agent

Ongoing Research

Expanding knowledge of its chemical and biological properties

Check Digit Verification of cas no

The CAS Registry Mumber 211388-15-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,1,3,8 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 211388-15:
(8*2)+(7*1)+(6*1)+(5*3)+(4*8)+(3*8)+(2*1)+(1*5)=107
107 % 10 = 7
So 211388-15-7 is a valid CAS Registry Number.

211388-15-7Downstream Products

211388-15-7Relevant academic research and scientific papers

Mass spectrometric studies of 3-substituted-5-amino-1,3,4-thiadiazolin-2-ones

Lee, Un Chul,Lee, Won,Kim, Yun Je,Park, Song Ja,Ra, Do Young,Cho, Nam Sook

, p. 231 - 241 (1998)

Fragment pathways of 3-alkyl and acyl-5-amino-1,3,4-thiadiazolin-2-ones were completely assigned by mass analyzed kinetic energy spectra (MIKE), collisional activated dissociation (CAD) spectra and high resolution mass spectra. [NH2CS]+ and [S=C=O]+ ions were directly formed from molecular ion of the 3-alkyl compounds and from 5-amino-3H-1,3,4 -thiadiazolin-2-one ion (1) which was produced by McLafferty rearrangement from molecular ion of 3-acyl compounds. A loss of neutral SCO was only detected from 3-alkyl substituted molecular ions.

Mass Spectrometric Studies of 3-Substituted-5-amino-1,3,4-thiadiazolin-2-ones

Lee, Un Chul,Lee, Won,Kim, Yun Je,Park, Song Ja,Ra, Do Young,Cho, Nam Sook

, p. 201 - 210 (2007/10/03)

Fragment pathways of 3-alkyl and acyl-5-amino-1,3,4-thiadiazolin-2-ones were completely assigned by mass analyzed kinetic energy spectra (MIKE), collisional activated dissociation (CAD) spectra and high resolution mass spectra. + and + ions were directly formed from molecular ion of the 3-alkyl compounds and from 5-amino-3H-1,3,4-thiadiazolin-2-one ion (1) which was produced by McLafferty rearrangement from molecular ion of 3-acyl compounds.A loss of neutral SCO was only detected from 3-alkyl substituted molecular ions. - Keywords: 3-substituted-5-amino-1,3,4-thiadiazolin-2-ones; MIKE and CAD spetra

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