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METHYL 5-HYDROXY-1-NAPHTHOATE, also known as Hydroxyquinoline, is a chemical compound with the molecular formula C12H10O3 and a molecular weight of 202.21 g/mol. It is an aromatic ester formed by the formal condensation of the acid group of hydroxyquinoline with methanol. This less commonly known compound does not have widespread industrial uses and is primarily utilized in scientific research, with potential applications in the field of organic chemistry. The toxicity and environmental impact of METHYL 5-HYDROXY-1-NAPHTHOATE have not been extensively studied.

91307-40-3

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91307-40-3 Usage

Uses

Used in Scientific Research:
METHYL 5-HYDROXY-1-NAPHTHOATE is used as a research compound for its unique chemical properties and potential applications in organic chemistry. It serves as a valuable tool for scientists to explore new chemical reactions and syntheses, contributing to the advancement of chemical knowledge and innovation.
Used in Organic Chemistry:
In the field of organic chemistry, METHYL 5-HYDROXY-1-NAPHTHOATE is used as a precursor or intermediate in the synthesis of various organic compounds. Its aromatic ester structure allows for further functionalization and modification, enabling the development of new molecules with specific properties and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 91307-40-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,3,0 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 91307-40:
(7*9)+(6*1)+(5*3)+(4*0)+(3*7)+(2*4)+(1*0)=113
113 % 10 = 3
So 91307-40-3 is a valid CAS Registry Number.

91307-40-3Downstream Products

91307-40-3Relevant academic research and scientific papers

Novel 8-substituted dipyridodiazepinone inhibitors with a broad-spectrum of activity against HIV-1 strains resistant to non-nucleoside reverse transcriptase inhibitors

O'Meara, Jeff A.,Yoakim, Christiane,Bonneau, Pierre R.,B?s, Michael,Cordingley, Michael G.,Déziel, Robert,Doyon, Louise,Duan, Jianmin,Garneau, Michel,Guse, Ingrid,Landry, Serge,Malenfant, Eric,Naud, Julie,Ogilvie, William W.,Thavonekham, Bounkham,Simoneau, Bruno

, p. 5580 - 5588 (2007/10/03)

A series of novel 8-substituted dipyridodiazepinone-based inhibitors were investigated for their antiviral activity against wild type human immunodeficiency virus (HIV-1) and the clinically prevalent K103N/Y181C mutant virus. Our efforts have resulted in a series of benzoic acid analogues that are potent inhibitors of HIV-1 replication against a panel of HIV-1 strains resistant to non-nucleoside reverse transcriptase inhibitors (NNRTIs). Furthermore, the combination of good antiviral potency, a broad spectrum of activity, and an excellent pharmacokinetic profile provides strong justification for the further development of compound 7 as a potential treatment for wild type and NNRT1-resistant HIV-1 infection.

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