21864-89-1 Usage
Uses
Used in Organic Synthesis:
(2Z)-(ethylimino)(phenyl)ethanenitrile is utilized as a key building block in the organic synthesis industry. Its unique structure allows for the creation of a variety of pharmaceutical compounds and other organic substances, making it a valuable component in the development of new molecules and materials.
Used in Pharmaceutical Industries:
In the pharmaceutical sector, (2Z)-(ethylimino)(phenyl)ethanenitrile serves as an essential intermediate for the synthesis of various drugs. Its presence in the molecular structure can influence the pharmacological properties of the final product, contributing to the development of novel medications with improved efficacy and safety profiles.
Used in Biological and Pharmacological Research:
(2Z)-(ethylimino)(phenyl)ethanenitrile has also been investigated for its potential biological and pharmacological properties. Researchers are exploring its interactions with biological systems and its potential applications in therapeutic areas, which could lead to the discovery of new treatments and advancements in medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 21864-89-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,8,6 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 21864-89:
(7*2)+(6*1)+(5*8)+(4*6)+(3*4)+(2*8)+(1*9)=121
121 % 10 = 1
So 21864-89-1 is a valid CAS Registry Number.
21864-89-1Relevant academic research and scientific papers
RuO4-mediated oxidation of secondary amines. Part 1. Are hydroxylamines the main intermediates?
Florea, Cristina A.,Petride, Horia
, p. 475 - 486 (2016/07/20)
The RuO4-catalyzed oxidation of secondary amines Bn-NH-CH2R (1a and b; R=H, Me) gave mainly amides, but minute amounts of nitrones PhCH=N(O)-CH2R (9a and b) and traces of Bn-N(OH)-CH2R (R=H, 4a) were also detect
Une nouvelle methode de transformation des aldehydes aromatiques en α-iminonitriles Ar-C(CN)=N-R
Pochat, Francis
, p. 955 - 956 (2007/10/02)
The reaction with amines of bromoderivates Ar-CBr(SEt)-CN, easily obtained in high yields from aldehydes, provides a convinient route to C-aryl N-alkyl (or aryl) α-iminonitriles.
