65538-54-7 Usage
Description
2-[(Diethylamino)methyl]-4-nitrophenol, with the chemical abstracts service number 65538-54-7, is an organic compound that plays a significant role in various chemical reactions and processes. Its unique molecular structure, featuring a nitro group and a diethylaminomethyl group attached to a phenol backbone, endows it with specific chemical properties that make it valuable in the field of organic synthesis.
Uses
Used in Organic Synthesis:
2-[(Diethylamino)methyl]-4-nitrophenol is used as a synthetic intermediate for the preparation of various organic compounds. Its presence in reactions can facilitate the formation of desired products through its reactivity and the influence it exerts on the reaction pathways. This makes it a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-[(Diethylamino)methyl]-4-nitrophenol is utilized as a key component in the synthesis of certain drugs. Its unique functional groups can be manipulated to create molecules with specific therapeutic properties, contributing to the development of new medications and treatments.
Used in Agrochemical Industry:
Similarly, in the agrochemical sector, 2-[(Diethylamino)methyl]-4-nitrophenol serves as a precursor in the synthesis of various agrochemicals. Its ability to be modified and incorporated into complex molecules makes it instrumental in the creation of pesticides, herbicides, and other agricultural products designed to protect crops and enhance yields.
Used in Specialty Chemicals:
2-[(Diethylamino)methyl]-4-nitrophenol also finds application in the production of specialty chemicals, which are often used in niche applications such as dyes, coatings, and advanced materials. Its versatility and reactivity make it a valuable component in the development of these high-value products.
Check Digit Verification of cas no
The CAS Registry Mumber 65538-54-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,5,3 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 65538-54:
(7*6)+(6*5)+(5*5)+(4*3)+(3*8)+(2*5)+(1*4)=147
147 % 10 = 7
So 65538-54-7 is a valid CAS Registry Number.
65538-54-7Relevant articles and documents
The influence of steric and polar effects on hydrogen bonding in 2-(N,N-diethylamino)-methyl-4-NO2-phenols
Filarowski,Koll,Glowiak
, p. 707 - 719 (1997)
Two crystal structures consisting of 2-(N,N-diethylamino)-methyl-4-NO2-phenol molecules were determined. In the triclinic crystals (with a = 9.527(2) A. b = 11.268(3) A c = 11.408(3) A, α = 87.80(3)°, β = 69.62(3)°, γ = 81.82(3)°, Z = 4, space group P1) asymmetric cyclic dimers were found, formed by two nonequivalent O-...H-N+ hydrogen bonds of 2.614(3) and 2.660(3) A lengths. In the complex of 2-(N,N-diethylamino)-methyl-4-NO2-phenol with 4-NO2-phenol (orthorhombic crystals with a = 20.732(4) A, b = 16.618(2) A, c = 10.452(2) A, Z = 8, space group Pbca) an intermolecular O-...H-O (2.525(2) A) hydrogen bond between 4-NO2-phenol and zwitterionic 2-(N,N-diethylamino)-methyl-4-NO2-phenol was found. In the latter molecule the intramolecular O-...-H-N+ (2.760(2) A) bridge is formed. The zwitterionic molecules form chains along the crystallographic b axis by NH+...O (3.105(2) A) hydrogen bridges. The N-H+ groups participate in bifurcated hydrogen bonds. The influence of the steric strain caused by N-alkyl chains and polar interactions of the NO2 group on the character of the hydrogen bond and the structure of cyclic dimers is discussed. The IR and UV spectra determined show the full agreement in description of the hydrogen bonding schemes, simultaneously demonstrating a drastic rearrangement of these schemes upon going to CCl4 solutions.
AN IMPROVED PROCEDURE FOR THE ISOLATION OF 2-(N,N-DIETHYLAMINOMETHYL)-4-NITROPHENOL
Souza, M. C. B. V. de,Bernardino, A. M. R.,Soares, M. C.,Retzlaff, M. G.
, p. 338 - 339 (2007/10/03)
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