104286-03-5 Usage
General Description
2-(1,3-benzoxazol-2-yl)benzoic acid is a chemical compound with a molecular formula C15H9NO3. It is a derivative of benzoxazole and benzoic acid, and is commonly used in research and pharmaceutical applications as a fluorescent probe for the detection of metal ions and other analytes. 2-(1,3-benzoxazol-2-yl)benzoic acid has also shown potential as a therapeutic agent for various diseases due to its ability to target specific biological pathways. Additionally, 2-(1,3-benzoxazol-2-yl)benzoic acid has been investigated for its antimicrobial and anti-inflammatory properties, further highlighting its potential applications in various fields of chemistry and medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 104286-03-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,2,8 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 104286-03:
(8*1)+(7*0)+(6*4)+(5*2)+(4*8)+(3*6)+(2*0)+(1*3)=95
95 % 10 = 5
So 104286-03-5 is a valid CAS Registry Number.
104286-03-5Relevant articles and documents
Microwave-assisted direct synthesis of 2-substituted benzoxazoles from carboxylic acids under catalyst and solvent-free conditions
Kumar, Raj,Selvam,Kaur, Gurmeet,Chakraborti, Asit K.
, p. 1401 - 1404 (2007/10/03)
A direct coupling of carboxylic acids with 2-aminophenol under microwave irradiation has been achieved leading to the synthesis of 2-substituted benzoxazoles under metal and solvent-free conditions. Aliphatic, aromatic and heteroaromatic carboxylic acids provide good yields. Benzoxazole formation takes place in the presence of chloro, methoxy, phenoxy, thiophenoxy, and α,β-unsaturated functionalities. In the case of dicarboxylic acids, the reaction proceeds via the formation of the corresponding anhydride with predominant formation of the mono-benzoxazole. Georg Thieme Verlag Stuttgart.
