1244-92-4 Usage
Uses
Used in Chemical Synthesis:
1(2H)-Naphthalenone, 4-methoxy-2-(4-methoxy-1-oxo-2(1H)-naphthalenylidene)is used as an intermediate in the chemical synthesis of various organic compounds. Its unique molecular structure allows for the creation of a wide range of derivatives with diverse applications.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1(2H)-Naphthalenone, 4-methoxy-2-(4-methoxy-1-oxo-2(1H)-naphthalenylidene)is used for research purposes. Its potential properties make it a candidate for further investigation into its possible applications in drug development. However, more research is required to fully understand its potential applications and effects in this field.
Used in Dye Manufacturing:
Given its yellow-colored appearance, 1(2H)-Naphthalenone, 4-methoxy-2-(4-methoxy-1-oxo-2(1H)-naphthalenylidene)may also find use in the dye manufacturing industry as a component in the production of various types of dyes and pigments.
Used in Material Science:
The unique molecular structure and properties of 1(2H)-Naphthalenone, 4-methoxy-2-(4-methoxy-1-oxo-2(1H)-naphthalenylidene)could potentially be applied in material science for the development of new materials with specific characteristics, such as improved stability or enhanced optical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 1244-92-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,4 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1244-92:
(6*1)+(5*2)+(4*4)+(3*4)+(2*9)+(1*2)=64
64 % 10 = 4
So 1244-92-4 is a valid CAS Registry Number.
1244-92-4Relevant academic research and scientific papers
Hypervalent iodine oxidation of naphthols: An efficient synthesis of 1,1-dialkoxynaphthalen-2(1H)-ones from 2-naphthol
Mallik, Uttam K,Mallik, Asok K
, p. 611 - 612 (2007/10/02)
Hypervalent iodide oxidation of 2-naphthol using (diacetoxyiodo)benzene in alcoholic medium gives 1,1-dialkoxynaphthalen-2(1H)-ones (3a and 3b) in very good yields.However, such an oxidation of 1-naphthol does not give the expected quinone monoketal (4).
Dimeric Naphthoquinones, XI. - Oxidation Products of Substituted Binaphthyls
Laatsch, Hartmut
, p. 1367 - 1381 (2007/10/02)
1',4,4'-Trimethoxy-2,2'-binaphthyl-1-ol (7a) is oxidized in high yield forming the quinone 8a or the cyclic acetal 22.Under acidic conditions, both compounds are easily transferred into substituted dinaphthofurans.
