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METHYL 5-HYDROXY-2-NITROBENZOATE, a nitrobenzoate derivative with the molecular formula C8H7NO5, is a yellow solid chemical compound commonly utilized in organic synthesis and pharmaceutical research. It serves as an intermediate in the production of various drugs and active pharmaceutical ingredients, as well as in the manufacturing of dyes, pigments, and other organic compounds. Due to its potential hazards, it is crucial to handle METHYL 5-HYDROXY-2-NITROBENZOATE with care and adhere to proper safety protocols.

59216-77-2

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59216-77-2 Usage

Uses

Used in Pharmaceutical Industry:
METHYL 5-HYDROXY-2-NITROBENZOATE is used as an intermediate in the synthesis of various drugs and active pharmaceutical ingredients for its ability to contribute to the development of new medications.
Used in Chemical Industry:
METHYL 5-HYDROXY-2-NITROBENZOATE is used as a component in the manufacturing of dyes and pigments, playing a role in the production of colorants for different applications.
Used in Organic Synthesis:
METHYL 5-HYDROXY-2-NITROBENZOATE is used as a reagent in organic synthesis processes, facilitating the creation of a range of organic compounds for various purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 59216-77-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,2,1 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 59216-77:
(7*5)+(6*9)+(5*2)+(4*1)+(3*6)+(2*7)+(1*7)=142
142 % 10 = 2
So 59216-77-2 is a valid CAS Registry Number.

59216-77-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 5-hydroxy-2-nitrobenzoate

1.2 Other means of identification

Product number -
Other names Benzoic acid,5-hydroxy-2-nitro-,methyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:59216-77-2 SDS

59216-77-2Relevant academic research and scientific papers

Preparation technology of 6-hydroxy-bentazone

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Paragraph 0021-0022; 0037-0038; 0053-0054; 0085-0086, (2017/08/28)

The invention discloses a preparation technology of 6-hydroxy-3-isopropyl-1H-benzo[c][1,2,6]thiadiazine-4(3H)-keto-2,2-dioxide. The preparation technology includes subjecting 5-chloro-2-nitrobenzoic acid serving as a raw material to hydrolysis reaction an

HETEROCYCLIC COMPOUNDS, PROCESS FOR PREPARATION OF THE SAME AND USE THEREOF

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Paragraph 0330; 0333; 0334, (2017/07/15)

The present invention provides a heterocyclic compound represented by the formula (I), its stereoisomers, or a pharmaceutically acceptable salt thereof, pharmaceutical compositions thereof, and their use in preparing a medicament for the prevention and/or treatment of central nervous system disease.

Discovery and Structure-Activity Relationships of the Neoseptins: A New Class of Toll-like Receptor-4 (TLR4) Agonists

Morin, Matthew D.,Wang, Ying,Jones, Brian T.,Su, Lijing,Surakattula, Murali M. R. P.,Berger, Michael,Huang, Hua,Beutler, Elliot K.,Zhang, Hong,Beutler, Bruce,Boger, Dale L.

supporting information, p. 4812 - 4830 (2016/06/13)

Herein, we report studies leading to the discovery of the neoseptins and a comprehensive examination of the structure-activity relationships (SARs) of this new class of small-molecule mouse Toll-like receptor 4 (mTLR4) agonists. The compounds in this class, which emerged from screening an α-helix mimetic library, stimulate the immune response, act by a well-defined mechanism (mouse TLR4 agonist), are easy to produce and structurally manipulate, exhibit exquisite SARs, are nontoxic, and elicit improved and qualitatively different responses compared to lipopolysaccharide, even though they share the same receptor.

SUBSTITUTED TRIAZOLOBENZODIAZEPINES

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Paragraph 0042, (2015/09/22)

This invention relates to novel substituted triazolobenzodiazepines of the Formula (I), wherein each of the variables are defined herein and pharmaceutically acceptable salts thereof. This invention also provides compositions comprising a compound of this

NEOSEPTINS: SMALL MOLECULE ADJUVANTS

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Page/Page column 44-46, (2014/09/03)

A MD-2:TLR4 complex agonist compound is disclosed whose structure corresponds to Formula (I), as defined within. Also disclosed are a method of its preparation and use, as well as a pharmaceutical composition containing the same.

Anthranilic acid-based Thumb Pocket 2 HCV NS5B polymerase inhibitors with sub-micromolar potency in the cell-based replicon assay

Stammers, Timothy A.,Coulombe, Rene,Duplessis, Martin,Fazal, Gulrez,Gagnon, Alexandre,Garneau, Michel,Goulet, Sylvie,Jakalian, Araz,Laplante, Steven,Rancourt, Jean,Thavonekham, Bounkham,Wernic, Dominik,Kukolj, George,Beaulieu, Pierre L.

, p. 6879 - 6885 (2014/01/06)

Optimization efforts on the anthranilic acid-based Thumb Pocket 2 HCV NS5B polymerase inhibitors 1 and 2 resulted in the identification of multiple structural elements that contributed to improved cell culture potency. The additive effect of these elements resulted in compound 46, an inhibitor with enzymatic (IC50) and cell culture (EC50) potencies of less than 100 nanomolar.

QUINAZOLINONE DERIVATIVES AS VIRAL POLYMERASE INHIBITORS

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Page/Page column 78, (2011/04/19)

Compounds of formula I: (I) wherein X, R2, R3, R5 and R6 are defined herein, are useful as inhibitors of the hepatitis C virus NS5B polymerase.

HOMOGENEOUS TIME RESOLVED FLUORESCENCE BASED TEST SYSTEM

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Page/Page column 36-37, (2010/12/29)

The present invention concerns a fluorescence resonance energy transfer based high throughput test system to measure the formation of the HIV gp41 six-helix bundle. In a first embodiment the current invention relates to a homogeneous time resolved fluorescence-based test system comprising a first helical polypeptide consisting essentially of the sequence of IQN36 (SEQ ID NO:1); a second helical polypeptide consisting essentially of the sequence of C34 (SEQ ID NO: 2) wherein said IQN36 is labeled with a light emitting fluorophore and said C34 is labeled with an ultra-violet excitable fluorophore.

VIRAL POLYMERASE INHIBITORS

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Page/Page column 82-83, (2010/04/27)

The present application provides compounds of formula I wherein X, Y, R2, n, R5 and R6 are defined herein, useful as inhibitors of the hepatitis C virus NS5B polymerase The present application also provides pharmaceutical

VIRAL POLYMERASE INHIBITORS

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Page/Page column 60, (2009/04/25)

Compounds of formula I: wherein X, R2, R3, R5 and R6 are defined herein, are useful as inhibitors of the hepatitis C virus NS5B polymerase.

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