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6-(Hydroxymethyl)naphthalene-2-carboxylic acid is an organic compound with the molecular formula C12H10O3. It is a white crystalline solid that is soluble in water and various organic solvents. This chemical is characterized by a naphthalene ring system, with a carboxylic acid group at the 2-position and a hydroxymethyl group at the 6-position. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. The compound can be synthesized through various methods, including the condensation of salicylaldehyde with formaldehyde in the presence of an acid catalyst. Due to its reactivity and structural diversity, 6-(hydroxymethyl)naphthalene-2-carboxylic acid is a valuable building block in organic chemistry and has potential applications in the development of new materials and compounds.

5859-95-0

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5859-95-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5859-95-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,5 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5859-95:
(6*5)+(5*8)+(4*5)+(3*9)+(2*9)+(1*5)=140
140 % 10 = 0
So 5859-95-0 is a valid CAS Registry Number.

5859-95-0Relevant academic research and scientific papers

Elongated multiple electronic cascade and cyclization spacer systems in activatible anticancer prodrugs for enhanced drug release

De Groot,Loos,Koekkoek,Van Berkom,Busscher,Seelen,Albrecht,De Bruijn,Scheeren

, p. 8815 - 8830 (2007/10/03)

The design and synthesis of several novel elongated self-elimination spacer systems for application in prodrugs is described. These elongated spacer systems can be incorporated between a cleavable specifier and the parent drug. Naphthalene- and biphenyl-containing spacers were synthesized but did not eliminate. Prodrugs of the anticancer agents doxorubicin and paclitaxel are reported that contain two or three electronic cascade spacers. A novel catalytic application of HOBt was found for the synthesis of N-aryl carbamates through reacting a 4-nitrophenyl carbonate with an aniline derivative, to connect the 1,6-elimination spacers via a carbamate linkage. In addition, a double spacer-containing paclitaxel prodrug was synthesized, comprising a 1,6-elimination spacer and a bis-amine linker connected to paclitaxel via a 2′-carbamate linkage. Prodrugs in which the novel spacer systems were incorporated between a specific tripeptide specifier and the parent drug doxorubicin or paclitaxel proved to be significantly faster activated by plasmin in comparison with prodrugs containing conventional spacer systems. It is expected that the generally applicable novel spacer systems reported herein will contribute to future development of improved enzymatically activated prodrugs.

NOVEL CHOLINE DERIVATIVE AND METHOD FOR DETERMINING SERUM CHOLINESTERASE ACTIVITY USING THE SAME

-

, (2008/06/13)

A novel compound, 6-acetoxymethyl-2-naphthoylcholine halide, is very stable to nonenzymatic hydrolysis and react specifically with cholinesterase in serum. A UV method for determining cholinesterase activity in serum which uses the novel compound as a substrate permits very accurate and highly reproducible determination of cholinesterase activity in serum, and therefor is very useful for clinical examination.

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