74262-35-4 Usage
Uses
Used in Pharmaceutical Industry:
Cyclohexanecarboxamide, N-phenyl-1-(phenylamino)is utilized as an intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs due to its unique chemical structure and reactivity.
Used in Agrochemical Industry:
Similarly, in the agrochemical sector, Cyclohexanecarboxamide, N-phenyl-1-(phenylamino)- serves as an intermediate in the production of various agrochemicals, playing a role in the synthesis of substances that help protect crops and enhance agricultural productivity.
Used in Material Science:
Cyclohexanecarboxamide, N-phenyl-1-(phenylamino)may also find applications in material science, where it could be instrumental in the development of new materials owing to its structural and chemical properties.
Used in Biochemical Research:
Furthermore, Cyclohexanecarboxamide, N-phenyl-1-(phenylamino)- holds potential as a research tool in biochemical studies, where it can be employed to explore and understand various biological and chemical processes due to its reactive groups and structural features.
Check Digit Verification of cas no
The CAS Registry Mumber 74262-35-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,2,6 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 74262-35:
(7*7)+(6*4)+(5*2)+(4*6)+(3*2)+(2*3)+(1*5)=124
124 % 10 = 4
So 74262-35-4 is a valid CAS Registry Number.
74262-35-4Relevant academic research and scientific papers
Convenient synthesis of α-amino amides using low-valent tantalum prepared from TaCl5 and Zn
Shimizu, Haruka,Kobayashi, Shu
, p. 7593 - 7595 (2007/10/03)
We have developed a general preparation method of α-amino amides from imines and isocyanates using low-valent tantalum prepared from TaCl5 and Zn in situ. This method was successfully applied to various imines derived from benzaldehyde derivati
Hindered Amines. Synthesis of Hindered Acyclic α-Aminoacetamides
Lai, John T.
, p. 3671 - 3673 (2007/10/02)
Hindered amines and their nitroxyl radicals are useful in spin-label studies as nonnucleophilic bases and as stabilizers for polymers against UV degradation.Hindered acyclic α-aminoacetamides (3, R5 = aryl, tert-butyl; R6 = H) can be synthesized from amines, ketones, and chloroform with 50percent sodium hydroxide solution in phase-transfer-catalyzed reactions.Nucleophilic secondary amines will undergo the same reactions while bulky ones fail.Mixed 3 can be prepared from different amines according to their nucleophilicities. 1,1-Dialkyl-2,2-dichlorooxirane (5) is believedto be the reactive intermediate.Imines are sometimes formed as byproducts through the opening of a carbon-carbon bond in the oxirane ring by amines.Thus, tert-butylcyclohexylamine (7) is obtained in 62percent yield after hydrogenation of the crude imine from tert-butylamine, cyclohexanone, and chloroform.
