610-57-1 Usage
Uses
Used in Organic Synthesis:
2,4-Dinitrobenzyl chloride is used as a protecting group in organic synthesis for the purpose of preventing unwanted reactions or side reactions involving alcohols and amines. This ensures that the desired products are obtained without the interference of undesired byproducts, thereby enhancing the efficiency and selectivity of the synthesis process.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2,4-dinitrobenzyl chloride is utilized as a key intermediate in the synthesis of various drugs. Its ability to protect functional groups during chemical reactions allows for the creation of complex molecular structures with greater precision and control, ultimately leading to the development of more effective and safer medications.
Used in Dye Manufacturing:
2,4-DINITROBENZYL CHLORIDE also finds application in the production of dyes, where it is employed as a protecting group to facilitate the synthesis of colorants with specific properties. By preventing unwanted reactions during the dye synthesis process, 2,4-dinitrobenzyl chloride contributes to the production of dyes with improved colorfastness, stability, and performance in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 610-57-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 610-57:
(5*6)+(4*1)+(3*0)+(2*5)+(1*7)=51
51 % 10 = 1
So 610-57-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H5ClN2O4/c8-4-5-1-2-6(9(11)12)3-7(5)10(13)14/h1-3H,4H2
610-57-1Relevant articles and documents
Vicarious Nucleophilic Chloromethylation of Nitroaromatics
Khutorianskyi, Viktor V.,Klepetá?ová, Blanka,Beier
supporting information, p. 5443 - 5446 (2019/07/03)
Nitroaromatics substituted with electron-acceptor or electron-donor groups undergo vicarious nucleophilic substitution with the lithium salt of dichloromethane to provide chloromethyl-substituted nitroaromatics in good to high yields. The methodology represents a new strategy for the synthesis of benzyl chlorides.
Highly efficient dinitration of aromatic compounds in fluorous media using ytterbium perfluorooctanesulfonate and perfluorooctanesulfonic acid as catalysts
Yi, Wen-Bin,Cai, Chun
, p. 2957 - 2961 (2007/10/03)
Ytterbium perfluorooctanesulfonate [Yb(OPf)3] and perfluorooctanesulfonic acid [PfOH] catalyze the highly efficient dinitration of toluene, benzene, benzyl chloride, and chlorobenzene in fluorous media. Notably the process produces almost no waste acid, as opposed to the traditional case. The fluorous phase-containing catalyst could be easily and efficiently recovered for reuse by simple phase separation. Copyright Taylor & Francis Group, LLC.
