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5-Nitrobenzoxazole-2-amine, also known as 5-nitro-1,3-benzoxazole-2-amine, is a chemical compound with the molecular formula C7H5N3O3. It is a nitroaromatic compound that contains a benzoxazole ring with a nitro group and an amine group attached to it. 5-Nitrobenzoxazole-2-amine is utilized in various fields, including organic synthesis, medicinal chemistry, and the development of pharmaceuticals and agrochemicals.

64037-16-7

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64037-16-7 Usage

Uses

Used in Pharmaceutical and Agrochemical Development:
5-Nitrobenzoxazole-2-amine is used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals for its potential therapeutic and pesticidal properties.
Used in Antimicrobial Applications:
5-Nitrobenzoxazole-2-amine is used as an antimicrobial agent, leveraging its ability to combat various microorganisms, thereby serving in the development of antibiotics and antifungal agents.
Used in Antitumor Applications:
In the field of oncology, 5-Nitrobenzoxazole-2-amine is used as an antitumor agent, showing promise in the mitigation of tumor growth and potentially contributing to cancer treatment strategies.
Used in Antiviral Applications:
5-Nitrobenzoxazole-2-amine is utilized as an antiviral agent, indicating its potential to inhibit viral replication and activity, which is crucial in developing treatments for viral infections.
Used as a Building Block in Organic Synthesis:
5-Nitrobenzoxazole-2-amine is used as a building block in the synthesis of various bioactive molecules, contributing to the creation of new compounds with potential applications in medicine and other industries.
Used in Fluorescent Probe Development:
Leveraging its fluorescent properties, 5-Nitrobenzoxazole-2-amine is used in the development of fluorescent probes for biological imaging and sensing applications, aiding in the advancement of diagnostic tools and research methodologies.

Check Digit Verification of cas no

The CAS Registry Mumber 64037-16-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,0,3 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 64037-16:
(7*6)+(6*4)+(5*0)+(4*3)+(3*7)+(2*1)+(1*6)=107
107 % 10 = 7
So 64037-16-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H5N3O3/c8-7-9-5-3-4(10(11)12)1-2-6(5)13-7/h1-3H,(H2,8,9)

64037-16-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-nitro-1,3-benzoxazol-2-amine

1.2 Other means of identification

Product number -
Other names 2-Amino-5-nitrobenzoxazole

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:64037-16-7 SDS

64037-16-7Relevant academic research and scientific papers

INHIBITORS OF HEPATITIS C VIRUS REPLICATION

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Paragraph 0912-0913, (2019/05/15)

The present invention relates to compounds of formula (I) that are useful as hepatitis C virus (HCV) NS5A inhibitors, the synthesis of such compounds, and the use of such compounds for inhibiting HCV NS5A activity, for treating or preventing HCV infections and for inhibiting HCV viral replication and/or viral production in a cell-based system.

Cyanoguanidine as a versatile, eco-friendly and inexpensive reagent for the synthesis of 2-aminobenzoxazoles and 2-guanidinobenzoxazoles

Grytsai, Oleksandr,Druzhenko, Tetiana,Demange, Luc,Ronco, Cyril,Benhida, Rachid

supporting information, p. 1642 - 1645 (2018/03/29)

An effective, easy-to-handle, safe and inexpensive protocol is reported for the synthesis of 2-aminobenzoxazoles under Lewis acid activation, utilising cyanoguanidine as the cyanating reagent. An optimized procedure for the synthesis of 2-guanidinobenzoxazole and novel derivatives is also described.

INHIBITORS OF HEPATITIS C VIRUS REPLICATION

-

Page/Page column 149, (2010/11/04)

The present invention relates to compounds of formula (I) that are useful as hepatitis C virus (HCV) NS5A inhibitors, the synthesis of such compounds, and the use of such compounds for inhibiting HCV NS5A activity, for treating or preventing HCV infections and for inhibiting HCV viral replication and/or viral production in a cell-based system.

Formation of nitrogen-containing heterocycles using di(imidazole-1-yl)methanimine

Wu, Yong-Qian,Limburg, David C.,Wilkinson, Douglas E.,Hamilton, Gregory S.

, p. 191 - 193 (2007/10/03)

A mild and efficient synthesis of five- and six-membered nitrogen containing heterocyclic compounds, in which di(imidazole-1-yl)methanimine serves as a one-carbon source, is reported.

Approach to the synthesis of (+)-ifforestine. Model studies directed at the tetracyclic framework

Roos, Gregory H. P.,Dastlik, Kim A.

, p. 2023 - 2044 (2007/10/03)

In order to design an effective asymmetric synthesis of (+)-ifforestine, model approaches to the construction of the tetracyclic ring system have been investigated. These studies have identified two key synthons, a functionalized isatoic anhydride and a p

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