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1H-1,2,4-Triazol-5-amine, 1-[2-amino-4-(trifluoromethyl)phenyl]-3-(methylthio)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88722-50-3

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88722-50-3 Usage

Structure

Contains a 1,2,4-triazol-5-amine ring, a 2-amino-4-(trifluoromethyl)phenyl group, and a 3-(methylthio) group

Biological activity

Exhibits potential antimicrobial and antifungal properties

Synthesis

May be used as a building block in the synthesis of various heterocyclic compounds and pharmaceutical drugs

Molecular weight

267.2 g/mol

Physical state

Solid

Appearance

Pale yellow or white crystalline solid

Solubility

Soluble in DMSO, slightly soluble in ethanol and methanol, and practically insoluble in water

Melting point

160-162°C

Purity

Typically >95% by HPLC

Storage

Store in a cool, dry place in a sealed container

Safety

Handle with care as potentially harmful, follow safety precautions in the workplace.

Check Digit Verification of cas no

The CAS Registry Mumber 88722-50-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,7,2 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 88722-50:
(7*8)+(6*8)+(5*7)+(4*2)+(3*2)+(2*5)+(1*0)=163
163 % 10 = 3
So 88722-50-3 is a valid CAS Registry Number.

88722-50-3Relevant academic research and scientific papers

On Triazoles. VII. . Synthesis of Novel Tri- and Tetracyclic Ring Systems.

Reiter, Jozsef,Pongo, Laszlo,Krajcsi, Peter,Esses-Reiter, Klara,Sohar, Pal,et al.

, p. 927 - 930 (2007/10/02)

The ring-closure of the 5-amino-1-(2-aminophenyl)-3-methylthio-1H-1,2,4-triazole derivatives 3 and 4 with different simple and cyclic C1 components lead to the formation of 1,2,4-triazolo-1,3,5-benzotriazepines 5-6, their 4,5-dihydro- 7, different 5-spiro-homocyclic 8-13, and spiro-heterocyclic 14-15 analogues.The structure of the compounds obtained was proved with the use of their ir, uv, 1H-nmr and 13C-nmr spectra.

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