16013-06-2 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 9 carbon (C), 8 hydrogen (H), 2 nitrogen (N), and 1 oxygen (O) atoms.
2. Heterocyclic organic compound
Explanation
A heterocyclic compound is a cyclic compound that contains atoms of at least two different elements. In this case, the compound has a five-membered ring structure with both oxygen and nitrogen atoms.
3. Five-membered ring structure
Explanation
The compound has a ring structure consisting of five atoms, which are connected to each other in a closed loop.
4. Contains both oxygen and nitrogen atoms
Explanation
The five-membered ring structure of the compound includes both oxygen and nitrogen atoms, making it a heterocyclic compound.
5. Stable compound
Explanation
1,2,4-Oxadiazole, 3-(4-methylphenyl)is known for its stability, which makes it suitable for use in various applications.
6. Highly versatile building block
Explanation
The compound is used as a building block in organic chemistry due to its ability to be easily modified and incorporated into more complex structures.
7. Used in the synthesis of pharmaceuticals and agrochemicals
Explanation
The compound serves as a key component in the development of various drugs and chemicals used in the pharmaceutical and agricultural industries.
8. Important precursor in drug development
Explanation
Its unique chemical properties make it a valuable starting material for the creation of new drugs and materials.
9. Potential applications in organic electronics and materials science
Explanation
The compound's electronic and structural properties make it a promising candidate for use in the development of new materials and devices in the fields of organic electronics and materials science.
10. 4-methylphenyl substitution
Explanation
The compound has a 4-methylphenyl group attached to the oxadiazole ring, which provides additional structural and chemical properties that can be exploited in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 16013-06-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,1 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 16013-06:
(7*1)+(6*6)+(5*0)+(4*1)+(3*3)+(2*0)+(1*6)=62
62 % 10 = 2
So 16013-06-2 is a valid CAS Registry Number.
16013-06-2Relevant articles and documents
An Efficient Synthesis of Functionalized 2 H -1,3,5-Oxadiazines via Metal-Carbenoid-Induced 1,2,4-Oxadiazole Ring Cleavage
Strelnikova, Julia O.,Rostovskii, Nikolai V.,Khoroshilova, Olesya V.,Khlebnikov, Alexander F.,Novikov, Mikhail S.
, p. 348 - 358 (2020/10/19)
A high-yielding method for the synthesis of 2 H -1,3,5-oxadiazines by rhodium(II)- or copper(II)-catalyzed reaction of 1,2,4-oxadiazoles with α-diazo esters has been developed. The reaction proceeds via attack of the metallocarbenoid on the oxadiazole N2 atom followed by ring opening/1,6-electrocyclization and enables the introduction of alkyl, aryl, oxy, and amino substituents into the 6-position and electron-withdrawing groups into the 2-position of 1,3,5-oxadiazine. The N2-attack and the N4-attack of the carbenoid cause different oxadiazole ring openings, which are controlled by the substitution at C5. The presence of a substituent at this position is a prerequisite for the N2-attack to occur, leading to the formation of 1,3,5-oxadiazines.
SYNTHESIS OF TRIAZOLES AND OXADIAZOLES FROM 2-ARYL-3-PHENYL-4-IMINO-5-CYANO-3,4-DIHYDROPYRIMIDINES
Robev, Stefan K.
, p. 2903 - 2906 (2007/10/02)
2-Aryl-3-phenyl-4-imino-5-cyano-3,4-dihydropyrimidines I were transformed to 1,2,4-triazoles II,IV and 1,2,4-oxadiazoles III by treatment with hydrazine, arylhydrazines or hydroxylamine in yields up to 90percent.
