69628-98-4 Usage
Description
1-(2-methoxyethyl)-4-nitrobenzene is an organic compound with the molecular formula C8H10NO3. It is characterized by the presence of a nitro group (-NO2) at the 4-position and a 2-methoxyethyl group (-OCH2CH3) attached to the 1-position of the benzene ring. 1-(2-methoxyethyl)-4-nitrobenzene is known for its versatile chemical properties and potential applications in various industries.
Uses
1. Used in Pharmaceutical Industry:
1-(2-methoxyethyl)-4-nitrobenzene is used as an intermediate for the synthesis of oxodihydropyridopyrimidines, which are c-fms kinase inhibitors. These inhibitors play a crucial role in the treatment of various diseases by targeting specific enzymes involved in disease progression.
2. Used in Chemical Synthesis:
Due to its unique structure, 1-(2-methoxyethyl)-4-nitrobenzene can be utilized as a building block in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals. Its reactivity and functional groups make it a valuable component in the development of new molecules with desired properties.
3. Used in Research and Development:
1-(2-methoxyethyl)-4-nitrobenzene can be employed as a model compound in academic and industrial research to study the effects of different functional groups on the chemical and physical properties of benzene derivatives. This knowledge can be applied to design and develop new molecules with specific applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 69628-98-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,6,2 and 8 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 69628-98:
(7*6)+(6*9)+(5*6)+(4*2)+(3*8)+(2*9)+(1*8)=184
184 % 10 = 4
So 69628-98-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO3/c1-13-7-6-8-2-4-9(5-3-8)10(11)12/h2-5H,6-7H2,1H3
69628-98-4Relevant articles and documents
Easy eco-friendly phenonium ion production from phenethyl alcohols in dimethyl carbonate
Barontini,Proietti Silvestri,Nardi,Bovicelli,Pari,Gallucci,Spezia,Righi
supporting information, p. 5004 - 5006 (2013/08/28)
An efficient and simple one-pot procedure for selective etherification of 2-aryl-ethylalcohols has been achieved through Amberlyst 15-catalyzed reaction in dimethyl carbonate (DMC). Moreover, the polymer catalyst could be recovered and reused with no effect on its activity. The reaction mechanism involves the formation of phenonium ion which has been demonstrated by a C-C bond forming reaction. Theoretical studies are in agreement with and thus explain experimental results.
HALOETHYL UREA COMPOUNDS AND THEIR USE TO ATTENUATE, INHIBIT OR PREVENT NON-CANCEROUS PATHOGENIC CELLULAR PROLIFERATION AND DISEASES ASSOCIATED THEREWITH
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Page 62, (2010/02/09)
The present invention provides haloethyl urea compounds as described in Formula (I) and their use as anti-proliferative agent in the attenuation, inhibition, or prevention of non-cancerous cellular proliferation. These compounds are also provided for use as a therapeutic agent in the treatment of a disease or disorder, wherein pathogenesis of said disease or disorder is associated with non-cancerous pathogenic cellular proliferation.
Reduction of carboxylic esters to ethers with triethyl silane in the combined use of titanium tetrachloride and trimethylsilyl trifluoromethanesulfonate
Yato,Homma,Ishida
, p. 5353 - 5359 (2007/10/03)
Aliphatic acyclic and cyclic ethers are prepared on treatment of their corresponding carboxylic esters and lactones with triethylsilane in the presence of titanium tetrachloride and trimethylsilyl trifluoromethanesulfonate.
