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CAS

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109060-64-2

5-(3-methylphenyl)-1,3,4-oxadiazol-2-amine(SALTDATA: FREE) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 109060-64-2 Structure

  • Basic information

    1. Product Name: 5-(3-methylphenyl)-1,3,4-oxadiazol-2-amine(SALTDATA: FREE)
    2. Synonyms: 5-(3-methylphenyl)-1,3,4-oxadiazol-2-amine(SALTDATA: FREE);5-(m-tolyl)-1,3,4-oxadiazol-2-amine
    3. CAS NO:109060-64-2
    4. Molecular Formula: C9H9N3O
    5. Molecular Weight: 175.19
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 109060-64-2.mol

  • Chemical Properties

    1. Melting Point: 74-75 °C
    2. Boiling Point: 353.2°C at 760 mmHg
    3. Flash Point: 167.4°C
    4. Appearance: /
    5. Density: 1.229g/cm3
    6. Vapor Pressure: 3.64E-05mmHg at 25°C
    7. Refractive Index: 1.594
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: -1.11±0.26(Predicted)
    11. CAS DataBase Reference: 5-(3-methylphenyl)-1,3,4-oxadiazol-2-amine(SALTDATA: FREE)(CAS DataBase Reference)
    12. NIST Chemistry Reference: 5-(3-methylphenyl)-1,3,4-oxadiazol-2-amine(SALTDATA: FREE)(109060-64-2)
    13. EPA Substance Registry System: 5-(3-methylphenyl)-1,3,4-oxadiazol-2-amine(SALTDATA: FREE)(109060-64-2)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 109060-64-2(Hazardous Substances Data)

109060-64-2 Usage

Uses

Used in Pharmaceutical Research and Drug Development:
5-(3-methylphenyl)-1,3,4-oxadiazol-2-amine (SALTDATA: FREE) is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure and properties may contribute to the development of new drugs with novel therapeutic effects.
Used in Analytical Chemistry:
In the field of analytical chemistry, 5-(3-methylphenyl)-1,3,4-oxadiazol-2-amine (SALTDATA: FREE) may be employed as a reagent or a component in the development of analytical methods for detecting and quantifying specific substances.
Used in Organic Synthesis:
5-(3-methylphenyl)-1,3,4-oxadiazol-2-amine (SALTDATA: FREE) is used as a building block in organic synthesis, enabling the creation of complex organic molecules with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.
Further research and testing are necessary to fully understand the potential uses and effects of 5-(3-methylphenyl)-1,3,4-oxadiazol-2-amine (SALTDATA: FREE) in these and other applications.

Check Digit Verification of cas no

The CAS Registry Mumber 109060-64-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,0,6 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 109060-64:
(8*1)+(7*0)+(6*9)+(5*0)+(4*6)+(3*0)+(2*6)+(1*4)=102
102 % 10 = 2
So 109060-64-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H9N3O/c1-6-3-2-4-7(5-6)8-11-12-9(10)13-8/h2-5H,1H3,(H2,10,12)

109060-64-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(3-Methylphenyl)-1,3,4-oxadiazol-2-amine

1.2 Other means of identification

Product number -
Other names F2182-0005

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:109060-64-2 SDS

109060-64-2Relevant articles and documents

Synthesis of N-pyrimidin[1,3,4]oxadiazoles and N-pyrimidin[1,3,4]-thiadiazoles from 1,3,4-oxadiazol-2-amines and 1,3,4-thiadiazol-2-amines via Pd-catalyzed heteroarylamination

Yan, Longjia,Deng, Minggao,Chen, Anchao,Li, Yongliang,Zhang, Wanzheng,Du, Zhi-yun,Dong, Chang-zhi,Meunier, Bernard,Chen, Huixiong

, p. 1359 - 1362 (2019)

An efficient and practical procedure was developed to prepare various N-pyrimidin[1,3,4]oxadiazole and thiadiazole scaffolds using a Buchwald-type coupling. The products of this reaction are otherwise difficult to access and could be used as building bloc

Synthesis, telomerase inhibitory and anticancer activity of new 2-phenyl-4H-chromone derivatives containing 1,3,4-oxadiazole moiety

Han, Xu,Liu, Xin Hua,Ma, Duo,Yu, Yun Long,Zhang, Zhao Yan

, p. 344 - 360 (2021/01/06)

Based on previous studies, 66 2-phenyl-4H-chromone derivatives containing amide and 1,3,4-oxadiazole moieties were prepared as potential telomerase inhibitors. The results showed most of the title compounds exhibited significantly inhibitory activity on telomerase. Among them, some compounds demonstrated the most potent telomerase inhibitory activity (IC50 50 = 6.41 μM). In addition, clear structure–activity relationships were summarised, indicating that the substitution of the methoxy group and the position, type and number of the substituents on the phenyl ring had significant effects on telomerase activity. Among them, compound A33 showed considerable inhibition against telomerase. Flow cytometric analysis showed that compound A33 could arrest MGC-803 cell cycle at G2/M phase and induce apoptosis in a concentration-dependent way. Meanwhile, Western blotting revealed that this compound could reduce the expression of dyskerin, which is a fragment of telomerase.

Discovery and biophysical characterization of 2-amino-oxadiazoles as novel antagonists of PqsR, an important regulator of Pseudomonas aeruginosa virulence

Zender, Michael,Klein, Tobias,Henn, Claudia,Kirsch, Benjamin,Maurer, Christine K.,Kail, Dagmar,Ritter, Christiane,Dolezal, Olan,Steinbach, Anke,Hartmann, Rolf W.

, p. 6761 - 6774 (2013/10/01)

The human pathogen Pseudomonas aeruginosa employs alkyl quinolones for cell-to-cell communication. The Pseudomonas quinolone signal (PQS) regulates various virulence factors via interaction with the transcriptional regulator PqsR. Therefore, we consider t

Anodic synthesis, spectral characterization and antimicrobial activity of novel 2-amino-5-substituted-1,3,4-oxadiazoles

Kumar, Sanjeev

experimental part, p. 126 - 129 (2010/08/22)

Synthesis of 2-amino-5-substituted-1,3,4-oxadiazoles through the electrochemical oxidation of semicarbazone was carried out at platinum anode at room temperature under controlled potential electrolysis in an undivided cell assembly. The electrolysis were

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