898289-64-0 Usage
Molecular structure
2-(5-methyl-1,3,4-oxadiazol-2-yl)benzoic acid is a compound that consists of a benzene ring fused with an oxadiazole ring, with a carboxyl group (-COOH) attached to the 2nd position of the benzene ring.
Methyl group position
The compound contains a methyl group attached to the 5th position of the oxadiazole ring, which can affect its biological activity and chemical properties.
Class
MBOA belongs to the class of benzoic acids, which are organic compounds that contain a carboxyl group attached to a benzene ring.
Potential use as a herbicide
MBOA has been studied for its ability to inhibit the growth of certain plants by interfering with their hormonal pathways, making it a potential candidate for use as a herbicide.
Plant defense mechanisms
MBOA has been investigated for its potential role in plant defense mechanisms, as it may have allelopathic properties that could be useful in controlling the growth of unwanted plants.
Natural occurrence
MBOA is a naturally occurring compound that has been found in certain plants, suggesting that it may have a role in their defense against herbivores or other environmental stressors.
Further research
The unique structure and biological activities of MBOA make it an interesting compound for further research and potential applications in agriculture.
Check Digit Verification of cas no
The CAS Registry Mumber 898289-64-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,8,2,8 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 898289-64:
(8*8)+(7*9)+(6*8)+(5*2)+(4*8)+(3*9)+(2*6)+(1*4)=260
260 % 10 = 0
So 898289-64-0 is a valid CAS Registry Number.
898289-64-0Relevant academic research and scientific papers
Gutov, Oleksii V.
, p. 3953 - 3957 (2013)
A series of new 1,3,4-oxadiazoles containing carboxylic and halogen groups and a double bond have been synthesized in good yields and a multigram scale. This was achieved at room temperature from readily available 1,2-diacylhydrazines using a cheap conden
