6085-93-4 Usage
Uses
Used in Organic Synthesis:
(2-Chloro-4-nitro-phenyl)-ethyl-amine is used as a building block for the synthesis of other organic compounds, contributing to the development of new chemical entities.
Used in Pharmaceutical Research:
In pharmaceutical research, (2-Chloro-4-nitro-phenyl)-ethyl-amine serves as a precursor for the development of new drugs and pharmaceuticals, potentially leading to advancements in medicinal chemistry.
Used in Agrochemical Production:
(2-Chloro-4-nitro-phenyl)-ethyl-amine is used as a chemical intermediate in the production of agrochemicals, playing a role in the creation of pesticides and other agricultural products.
Used in Specialty Chemicals Production:
(2-Chloro-4-nitro-phenyl)-ethyl-amine also finds use in the production of specialty chemicals, where it may contribute to the development of unique chemical products for specific industries.
Check Digit Verification of cas no
The CAS Registry Mumber 6085-93-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,8 and 5 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6085-93:
(6*6)+(5*0)+(4*8)+(3*5)+(2*9)+(1*3)=104
104 % 10 = 4
So 6085-93-4 is a valid CAS Registry Number.
6085-93-4Relevant academic research and scientific papers
Regioselective nitration of N,N-dialkylanilines using cerium(IV) ammonium nitrate in acetonitrile
Yang, Xianghua,Xi, Chanjuan,Jiang, Yanfeng
, p. 8781 - 8783 (2007/10/03)
A highly regioselective and inexpensive nitration of N,N-dialkylanilines by cerium(IV) ammonium nitrate (CAN) in acetonitrile under room temperature to yield p-nitryl-N,N-dialkylanilines in good yields was reported.
Alkylaminonitrobenzenes by Vicarious Nucleophilic Amination with 4-(Alkylamino)-1,2,4-triazoles
Katritzky, Alan R.,Laurenzo, Kathleen S.
, p. 3978 - 3982 (2007/10/02)
A series of 4-(alkylamino)-1,2,4-triazoles transfer the alkylamino group to the 4-position of nitrobenzene and various 3-substituted nitrobenzenes, with no detectable ortho substitution.By contrast 2-nitrothiophene reacts in the 3-position and 2-nitronaphthalene in the 1-position; 1-nitronaphthalene gives a mixture of products derived from dominant 2- with some 4-substitution.The orientations are discussed and rationalized.
