67886-69-5 Usage
Description
Naphthalene, 2-iodo-6-methoxy(9CI), also known as 2-Iodo-6-methoxy-naphthalene, is a chemical compound with the molecular formula C11H9IO. It is a derivative of naphthalene, a polycyclic aromatic hydrocarbon. Naphthalene, 2-iodo-6-methoxy(9CI) is characterized by the presence of an iodine atom at the 2nd position and a methoxy group at the 6th position on the naphthalene ring.
Uses
Used in Organic Synthesis:
Naphthalene, 2-iodo-6-methoxy(9CI) is used as a building block in organic synthesis for the preparation of various compounds. Its unique structure allows for the formation of new chemical bonds and the creation of diverse molecules with potential applications in various fields.
Used in Pharmaceutical Research:
In the pharmaceutical industry, Naphthalene, 2-iodo-6-methoxy(9CI) is utilized as a key intermediate in the synthesis of biologically active molecules and pharmaceutical intermediates. Its presence in these molecules can contribute to their therapeutic properties and potential use in treating various diseases and conditions.
Used in Drug Development:
Naphthalene, 2-iodo-6-methoxy(9CI) has potential applications in the development of new drugs and therapeutic agents. Its unique chemical structure can be leveraged to design and create novel compounds with improved pharmacological properties, such as increased potency, selectivity, and reduced side effects.
Used as a Reference Standard:
In analytical testing and research, Naphthalene, 2-iodo-6-methoxy(9CI) may also be used as a reference standard. This allows for the accurate identification, quantification, and quality control of related compounds and substances in various applications, ensuring the reliability and validity of experimental results.
Check Digit Verification of cas no
The CAS Registry Mumber 67886-69-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,8,8 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 67886-69:
(7*6)+(6*7)+(5*8)+(4*8)+(3*6)+(2*6)+(1*9)=195
195 % 10 = 5
So 67886-69-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H9IO/c1-13-11-5-3-8-6-10(12)4-2-9(8)7-11/h2-7H,1H3
67886-69-5Relevant articles and documents
N6-arylation of 2′-deoxyadenosine via copper-catalyzed direct coupling with aryl halides
Ran, Chongzhao,Dai, Qing,Harvey, Ronald G.
, p. 3724 - 3726 (2005)
(Chemical Equation Presented) A general method for efficient N 6-arylation of 2′-deoxyadenosine via copper-catalyzed direct coupling with aryl iodides and bromides is described. The method is useful for aryl halides with either electron-donatin
REACTIVE MESOGENIC COMPOUNDS AND MIXTURES
-
, (2011/08/04)
The invention relates to new reactive mesogenic compounds (RM), polymerisable liquid crystal (LC) mixtures and polymers comprising them, and the use of the compounds, mixtures and polymers in optical, electrooptical, electronic, semiconducting or luminescent components or devices, in decorative, security or cosmetic applications, especially for use in polymer films having high optical dispersion.
Lipase-mediated asymmetric construction of 2-arylpropionic acids: Enantiocontrolled syntheses of S-naproxen and S-ibuprofen
Bando, Toshikazu,Namba, Yukiko,Shishido, Kozo
, p. 2159 - 2165 (2007/10/03)
A general and enantiocontrolled synthetic route to 2-arylpropionic acids, represented by non-steroidal anti-inflammatory drugs S-naproxen 1a and S-ibuprofen 1b, has been developed by employing the lipase-mediated asymmetric acetylation of prochiral 2-aryl-1,3-propanediol 3, which has been derived via a Heck reaction, as the key step.
