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6-Nitro-2-methoxynaphthalene is an organic compound characterized by a naphthalene ring system, which consists of two fused benzene rings. This particular compound has a nitro group (-NO2) attached at the 6th position and a methoxy group (-OCH3) at the 2nd position of the naphthalene core. The nitro group introduces a strong electron-withdrawing effect, while the methoxy group acts as an electron-donating group. This combination of functional groups imparts unique chemical and physical properties to the molecule, making it a potential candidate for various applications in the fields of chemistry and materials science, such as in the synthesis of dyes, pharmaceuticals, or as intermediates in organic synthesis.

4900-67-8

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4900-67-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4900-67-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,0 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4900-67:
(6*4)+(5*9)+(4*0)+(3*0)+(2*6)+(1*7)=88
88 % 10 = 8
So 4900-67-8 is a valid CAS Registry Number.

4900-67-8Relevant academic research and scientific papers

Aromatic nitration in liquid Ag0.51K0.42Na 0.07NO3

Mascal, Mark,Yin, Lunxiang,Edwards, Ross,Jarosh, Michael

, p. 6148 - 6151 (2008/12/22)

(Figure Presented) Aromatic molecules have a strong affinity for silver(I) and dissolve to a limited extent in Ag0.51K0.42Na 0.07NO3, a low-melting eutectic mixture of silver, potassium, and sodium nitrates. Aromatic nitration in this inorganic ionic liquid leads to products which arise from nonelectrophilic substitution pathways.

Oxidative Derivatisation of Aromatic Ethers

Chawla, H. Mohindra,Mittal, Ram S.

, p. 539 - 542 (2007/10/02)

Reaction of cerium(IV) ammonium nitrate with some naphthyl ethers has been studied as a substitute to traditionally used hydrolytic cleavage method for their identification.One-pot, one-step synthesis of 2,2'-dinitro-1,1'-diethoxy-4,4'-bisnaphthalene; 2,2'-diethoxy-8-nitro-4,4'-bisnaphthalene; 1,8-dinitro-2-methoxynaphthalene; 2-methoxy-8-nitronaphthalene; 1-methoxy-4-nitronaphthalene; 1-ethoxy-4-nitronaphthalene; 4-nitro-1-naphthylbenzoate; 2-methoxy-6-nitronaphthalene; 1-nitro-2-naphthylbenzoate are described.

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