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175135-19-0

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175135-19-0 Usage

General Description

5-Morpholino-2-nitrophenol is a chemical that belongs to the class of nitrophenols. It is derived from the combination of a morpholine ring and a nitrophenol group. 5-MORPHOLINO-2-NITROPHENOL has been studied for its potential use as a UV absorber in sunscreen formulations, as well as in the production of dyes and pharmaceuticals. Its unique structure and properties make it a valuable intermediate for organic synthesis. Additionally, 5-Morpholino-2-nitrophenol has shown potential as an inhibitor of enzymes involved in the biosynthesis of bacterial cell walls, making it a target for the development of new antimicrobial agents. However, it is important to note that this chemical should be handled with caution due to its toxic and irritant properties.

Check Digit Verification of cas no

The CAS Registry Mumber 175135-19-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,1,3 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 175135-19:
(8*1)+(7*7)+(6*5)+(5*1)+(4*3)+(3*5)+(2*1)+(1*9)=130
130 % 10 = 0
So 175135-19-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H12N2O4/c13-10-7-8(1-2-9(10)12(14)15)11-3-5-16-6-4-11/h1-2,7,13H,3-6H2/p-1

175135-19-0 Well-known Company Product Price

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  • Alfa Aesar

  • (B24950)  5-(4-Morpholinyl)-2-nitrophenol, 97%   

  • 175135-19-0

  • 1g

  • 193.0CNY

  • Detail
  • Alfa Aesar

  • (B24950)  5-(4-Morpholinyl)-2-nitrophenol, 97%   

  • 175135-19-0

  • 5g

  • 761.0CNY

  • Detail
  • Alfa Aesar

  • (B24950)  5-(4-Morpholinyl)-2-nitrophenol, 97%   

  • 175135-19-0

  • 25g

  • 3095.0CNY

  • Detail

175135-19-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-morpholin-4-yl-2-nitrophenol

1.2 Other means of identification

Product number -
Other names 5-(morpholin-4-yl)-2-nitrophenol

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:175135-19-0 SDS

175135-19-0Relevant articles and documents

Nucleophilic substitution of halogens with amines in 2- and 4-nitrophenols

Wrobel, Zbigniew,Kwast, Andrzej

, p. 259 - 262 (2007)

Fluorine and chlorine in halonitrophenols are efficiently replaced with alkylamines in acetonitrile or in an excess of the amine at elevated temperature. Georg Thieme Verlag Stuttgart.

ANTIBIOTIC COMPOUNDS

-

Page/Page column 198; 199, (2018/03/25)

The present invention relates to antibiotic compounds of formula (I), to compositions containing these compounds and to methods of treating bacterial diseases and infections using the compounds. The compounds find application in the treatment of infection with, and diseases caused by, Gram-positive and/or Gram-negative bacteria, and in particular in the treatment of infection with, and diseases caused by, Neisseria gonorrhoeae.

2-Aminobenzoxazole ligands of the hepatitis C virus internal ribosome entry site

Rynearson, Kevin D.,Charrette, Brian,Gabriel, Christopher,Moreno, Jesus,Boerneke, Mark A.,Dibrov, Sergey M.,Hermann, Thomas

supporting information, p. 3521 - 3525 (2014/07/22)

2-Aminobenzoxazoles have been synthesized as ligands for the hepatitis C virus (HCV) internal ribosome entry site (IRES) RNA. The compounds were designed to explore the less basic benzoxazole system as a replacement for the core scaffold in previously discovered benzimidazole viral translation inhibitors. Structure-activity relationships in the target binding of substituted benzoxazole ligands were investigated.

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