41018-62-6 Usage
Uses
Used in Organic Synthesis:
1-(4-methylphenyl)-1-phenylhydrazine is used as a reagent for the synthesis of various organic compounds, such as pharmaceuticals, pesticides, and dyes, due to its versatile chemical properties and ability to participate in a wide range of chemical reactions.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1-(4-methylphenyl)-1-phenylhydrazine is used as a building block in the development of new drugs, contributing to the creation of novel medicinal compounds with potential therapeutic applications.
Used in Agrochemicals:
1-(4-methylphenyl)-1-phenylhydrazine is also utilized in the agrochemical industry for the synthesis of pesticides, showcasing its versatility in different chemical domains.
Used in Material Science:
1-(4-methylphenyl)-1-phenylhydrazine finds application in material science, where it is employed in the production of heterocyclic compounds and other organic substances, contributing to the development of new materials with specific properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 41018-62-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,0,1 and 8 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 41018-62:
(7*4)+(6*1)+(5*0)+(4*1)+(3*8)+(2*6)+(1*2)=76
76 % 10 = 6
So 41018-62-6 is a valid CAS Registry Number.
41018-62-6Relevant academic research and scientific papers
Palladium-catalyzed monoarylation of arylhydrazines with aryl tosylates
Huang, Yange,Choy, Pui Ying,Wang, Junya,Tse, Man-Kin,Raymond Wai-Yin Sun,Albert Sun-Chi Chan,Kwong, Fuk Yee
, p. 14664 - 14673 (2020/12/29)
A palladium-catalyzed C-N bond coupling reaction between arylhydrazines and aryl tosylates for facile synthesis of unsymmetrical N,N-diarylhydrazines has been developed. Employing the catalyst system of Pd(TFA)2 associated with newly developed phosphine ligand L1, the monoarylation of arylhydrazine proceeds smoothly to afford desired products in good-to-excellent yields (up to 95%) with good functional group compatibility. This method provides an alternative synthetic pathway for accessing structurally diversified N,N-diarylhydrazines from simple and easily accessible coupling components.
