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2-(2-CHLORO-5-METHYLPHENOXY)ACETOHYDRAZIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

588680-02-8

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588680-02-8 Usage

Compound type

Hydrazide derivative

Phenoxy group

Contains a chlorine and methyl substitution

Functional group

Acetohydrazide

Potential applications

Pharmaceutical industry (development of new drugs and medications)

Additional uses

Research and organic synthesis

Safety concerns

Potential toxicity and reactivity, requires cautious handling and compliance with safety protocols

Check Digit Verification of cas no

The CAS Registry Mumber 588680-02-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,8,8,6,8 and 0 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 588680-02:
(8*5)+(7*8)+(6*8)+(5*6)+(4*8)+(3*0)+(2*0)+(1*2)=208
208 % 10 = 8
So 588680-02-8 is a valid CAS Registry Number.

588680-02-8Downstream Products

588680-02-8Relevant academic research and scientific papers

Synthesis and in-vitro antimicrobial activity of new 1,2,4-triazoles

Bhat,Bhat,Shenoy

, p. 267 - 272 (2001)

We have described the synthesis of new 1,2,4-triazoles and have evaluated their antimicrobial profile. Antitubercular activity was determined in triplicate using the Lowenstein-Jensen medium. A loopful of Mycobacterium tuberculosis suspension was inoculated on the surface of each Lowenstein-Jensen media containing the test compounds (100, 10 or 1 μg mL-1). To evaluate in-vitro antibacterial activity, compounds (50, 5 or 0.5 μg) were evaluated against B. subtilis, Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus and Staphylococcus typhi by the disc diffusion method. To evaluate antifungal activity Sabourauds Dextrose agar medium was used. Some of the compounds (5, 0.5 or 0.05 μg mL-1) were screened for activity against Aspergillus niger 88 and Aspergillus niger 90 and others were screened for activity against T. rubrum TR1, T. rubrum R6, T. rubrum R7 and T. mentagrophyte M1, using the cup plate method. Our results show that the triazoles with a pyrazine moiety at position 3 were more active as antitubercular and antifungal agents compared with the triazoles which had a pyrazine moiety at position 4 of the molecule.

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