129053-56-1 Usage
Description
<<(1-formyl-2-phenyl)oxy>methyl>benzonitrile is a complex organic compound characterized by the presence of a formyl group, a phenyl group, an oxy-methyl group, and a benzonitrile group. The formyl group features a carbon atom double-bonded to an oxygen atom and single-bonded to a hydrogen atom. The phenyl group consists of a ring of six carbon atoms with alternating double and single bonds. The oxy-methyl group contains an oxygen atom bonded to a carbon atom, which is further bonded to three hydrogen atoms. The benzonitrile group is composed of a benzene ring attached to a nitrile group, which has a carbon atom triple-bonded to a nitrogen atom. Given the variety of functional groups present, <<(1-formyl-2-phenyl)oxy>methyl>benzonitrile is expected to exhibit diverse chemical properties and potential applications.
Uses
Used in Pharmaceutical Industry:
<<(1-formyl-2-phenyl)oxy>methyl>benzonitrile is used as an intermediate compound for the synthesis of various pharmaceuticals due to its complex structure and the presence of multiple functional groups that can be further modified or reacted to produce desired medicinal compounds.
Used in Chemical Research:
In the field of chemical research, <<(1-formyl-2-phenyl)oxy>methyl>benzonitrile serves as a model compound for studying the reactivity and behavior of different functional groups in organic reactions. Its unique structure allows researchers to explore new reaction pathways and develop innovative synthetic methods.
Used in Material Science:
<<(1-formyl-2-phenyl)oxy>methyl>benzonitrile may also find applications in material science, particularly in the development of novel polymers and advanced materials. The presence of various functional groups in <<(1-formyl-2-phenyl)oxy>methyl>benzonitrile can be exploited to create new materials with specific properties, such as improved strength, flexibility, or chemical resistance.
Used in Dye and Pigment Industry:
Given the presence of a phenyl group and a nitrile group, <<(1-formyl-2-phenyl)oxy>methyl>benzonitrile could potentially be used as a starting material for the synthesis of dyes and pigments. <<(1-formyl-2-phenyl)oxy>methyl>benzonitrile's structural features may contribute to the development of new colorants with enhanced properties, such as improved lightfastness and stability.
Used in Agrochemical Industry:
<<(1-formyl-2-phenyl)oxy>methyl>benzonitrile's complex structure and functional groups may also make it a candidate for use in the agrochemical industry, where it could be employed as a building block for the development of new pesticides or other agricultural chemicals. The specific properties of <<(1-formyl-2-phenyl)oxy>methyl>benzonitrile may enable the creation of more effective and targeted products for crop protection and management.
Check Digit Verification of cas no
The CAS Registry Mumber 129053-56-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,0,5 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 129053-56:
(8*1)+(7*2)+(6*9)+(5*0)+(4*5)+(3*3)+(2*5)+(1*6)=121
121 % 10 = 1
So 129053-56-1 is a valid CAS Registry Number.
129053-56-1Relevant articles and documents
A New Alkaline Rearrangement of the Benzofuran Skeleton. One Step Transformation of 2-(2-Benzofuranyl)benzonitriles Into (Z)-Phenylmethyleneisoindolinones
Guillaumel, J.,Boccara, N.,Demerseman, P.,Royer, R.,Bideau, J. P.,et al.
, p. 605 - 614 (2007/10/02)
The alkaline hydrolysis of 2-(2-benzofuranyl)benzonitriles 2 by potassium hydroxide under reflux in ethanol stops at the corresponding amides 5.Using other solvents (ethylene glycol or methoxyethanol) at higher temperatures, one can obtain either the amides 5, the acids 1 or rearrangement products depending on the experimental conditions.The rearrangement products were identified as (Z)-phenylmethylenedihydroisoindolinones 6 resulting from opening of the furan ring.The structures of the compounds 6 were established by 1H nmr spectroscopy (nOe) and X-ray crystallography.
