7256-51-1 Usage
Uses
Used in Pharmaceutical Industry:
(5-PHENYL-1,3,4-OXADIAZOL-2-YL)ACETONITRILE is used as a potential drug candidate for the development of new medications due to its unique structure and properties. The oxadiazole ring in the compound makes it a promising candidate for the development of new drugs, as it can be modified and functionalized to create a variety of drug molecules with different therapeutic effects.
Used in Agrochemical Industry:
(5-PHENYL-1,3,4-OXADIAZOL-2-YL)ACETONITRILE is used as a potential active ingredient in the development of new agrochemicals, such as pesticides and herbicides. (5-PHENYL-1,3,4-OXADIAZOL-2-YL)ACETONITRILE's unique structure and properties may allow for the creation of novel agrochemicals with improved efficacy, selectivity, and environmental safety.
Used in Materials Science:
(5-PHENYL-1,3,4-OXADIAZOL-2-YL)ACETONITRILE is used as a precursor in the chemical synthesis of various materials, such as polymers and composites. The acetonitrile group in the compound can be utilized in the synthesis of new materials with specific properties, such as improved mechanical strength, thermal stability, or chemical resistance.
Used in Chemical Synthesis:
(5-PHENYL-1,3,4-OXADIAZOL-2-YL)ACETONITRILE is used as a versatile building block in the synthesis of various organic compounds. (5-PHENYL-1,3,4-OXADIAZOL-2-YL)ACETONITRILE's unique structure allows for further functionalization and modification, enabling the creation of a wide range of organic molecules with different applications in various industries, such as pharmaceuticals, agrochemicals, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 7256-51-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,5 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7256-51:
(6*7)+(5*2)+(4*5)+(3*6)+(2*5)+(1*1)=101
101 % 10 = 1
So 7256-51-1 is a valid CAS Registry Number.
7256-51-1Relevant academic research and scientific papers
Synthesis of new 1,2,3-triazolo[1,5-a]quinazolinones
Pokhodylo, Nazariy T.,Matiychuk, Vasyl S.
experimental part, p. 415 - 420 (2010/06/16)
(Chemical Equation Presented) Synthesis of novel 3-substituted-1,2,3- triazolo[1,5-a]quinazolinones in high yields was performed via anionic hetero-domino reaction of appropriate substituted 2-azidobenzoates prepared from isatines and acetonitriles activated by 1,3-thiazole, 1,3-benzothiazole, 1,3,4-oxadiazole, and 1,2,4-oxadiazole rings. It was shown that acetonitriles exhibited high reactivity and were convenient methylenic compounds for such reactions providing rapid structural variation.
Polynuclear nonfused bis(1,3,4-oxadiazole)-containing systems
Vereshchagin,Petrov,Kizhnyaev,Pokatilov,Smirnov
, p. 1049 - 1055 (2007/10/03)
Nonfused bis-1,3,4-oxadiazoles were synthesized by reaction of 5-substituted mono- and bis-tetrazoles with mono- and dicarboxylic acid chlorides. The results of kinetic studies showed that the transformation of tetrazoles into 1,3,4-oxadiazoles is accelerated by 1 to 2 orders of magnitude on addition of a catalytic amount of dimethylformamide, triethylamine, or pyridine. Pleiades Publishing, Inc., 2006.
Recyclization of 2-imino-2H-1-benzopyrans under the influence of nucleophilic reagents. 1. New approach to the synthesis of 3-(1,3,4-oxadi-, thiadi-, and triazolyl-2)coumarins
Kovalenko,Zubkov,Chernykh,Turov,Ivkov
, p. 163 - 168 (2007/10/03)
It has been found that under the action of hydrazides of carboxylic acids, 2-iminocoumarin-3-carboxamides are recydized to N(1)-acylamidrazones of coumarin-3-carboxylic acids. The use of N(1)-acylamidrazones is proposed as a simple and effective means of synthesizing 3-(1,3,4-oxadi-, thiodi-, and triazolyl-2)coumarins. The possibilities of alternate schemes of synthesis are discussed, and a mechanism is suggested for the recyclization. 1996 Plenum Publishing Corporation.
