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2-((4-Methoxy-2-nitrophenyl)aMino)acetic acid, also known as 4-Methoxy-2-nitroaniline-2-carboxylic acid, is a chemical compound with a molecular formula C9H10N2O6. It is a yellow crystalline solid that is soluble in organic solvents such as ethanol and dimethyl sulfoxide. 2-((4-Methoxy-2-nitrophenyl)aMino)acetic acid is a derivative of 4-methoxy-2-nitroaniline and is commonly used in the synthesis of various pharmaceuticals and dyes. It is known for its ability to form stable complexes with metal ions and has been studied for its potential applications in the field of medicinal chemistry, making it an important intermediate in the production of various organic compounds.

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  • 55687-28-0 Structure
  • Basic information

    1. Product Name: 2-((4-Methoxy-2-nitrophenyl)aMino)acetic acid
    2. Synonyms: 2-((4-Methoxy-2-nitrophenyl)aMino)acetic acid;N-(4-Methoxy-2-nitrophenyl)glycine
    3. CAS NO:55687-28-0
    4. Molecular Formula: C9H10N2O5
    5. Molecular Weight: 226.1861
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 55687-28-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 492.2°C at 760 mmHg
    3. Flash Point: 251.5°C
    4. Appearance: /
    5. Density: 1.451g/cm3
    6. Vapor Pressure: 1.67E-10mmHg at 25°C
    7. Refractive Index: 1.627
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-((4-Methoxy-2-nitrophenyl)aMino)acetic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-((4-Methoxy-2-nitrophenyl)aMino)acetic acid(55687-28-0)
    12. EPA Substance Registry System: 2-((4-Methoxy-2-nitrophenyl)aMino)acetic acid(55687-28-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 55687-28-0(Hazardous Substances Data)

55687-28-0 Usage

Uses

Used in Pharmaceutical Industry:
2-((4-Methoxy-2-nitrophenyl)aMino)acetic acid is used as an intermediate in the synthesis of various pharmaceuticals for its ability to form stable complexes with metal ions, which can enhance the efficacy and stability of the final drug products.
Used in Dye Industry:
2-((4-Methoxy-2-nitrophenyl)aMino)acetic acid is used as a starting material in the production of various dyes due to its chemical properties and reactivity with other compounds.
Used in Organic Chemistry Research:
2-((4-Methoxy-2-nitrophenyl)aMino)acetic acid is used as a research compound in organic chemistry for studying its reactivity, stability, and potential applications in the synthesis of new organic compounds.
Used in Medicinal Chemistry:
2-((4-Methoxy-2-nitrophenyl)aMino)acetic acid is used as a potential candidate in medicinal chemistry for its ability to form stable complexes with metal ions, which can be utilized in the development of new drugs and therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 55687-28-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,6,8 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 55687-28:
(7*5)+(6*5)+(5*6)+(4*8)+(3*7)+(2*2)+(1*8)=160
160 % 10 = 0
So 55687-28-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H10N2O5/c1-16-6-2-3-7(10-5-9(12)13)8(4-6)11(14)15/h2-4,10H,5H2,1H3,(H,12,13)

55687-28-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-methoxy-2-nitroanilino)acetic acid

1.2 Other means of identification

Product number -
Other names -

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:55687-28-0 SDS

55687-28-0Relevant articles and documents

Synthesis and biological evaluation of quinoxaline derivatives as specific c-Met kinase inhibitors

Boggu, Pulla Reddy,Jung, Jun Min,Jung, Young Hoon,Kim, In Su,Kim, Seung Chan,Kim, So Young,Kim, Yeon Su,Ma, Sang Ho,Park, Gi Min,Yu, Ha Na

supporting information, (2020/05/08)

A series of novel quinoxaline derivatives were synthesized and evaluated for their inhibitory activity against c-Met kinase enzyme. Most of the tested compounds exhibited potent inhibitory activity. All the synthesized quinoxaline compounds were further e

Synthesis of [18F]Fluoroarenes by Nucleophilic Radiofluorination of N-Arylsydnones

Narayanam, Maruthi Kumar,Ma, Gaoyuan,Champagne, Pier Alexandre,Houk, Kendall N.,Murphy, Jennifer M.

supporting information, p. 13006 - 13010 (2017/09/28)

A practical method for radiofluorination of anilines with [18F]fluoride via N-arylsydnone intermediates is described. These precursors are stable, easy to handle and facilitate direct and regioselective 18F-labeling to prepare [

o-Nitroaniline Derivatives. Part 9. Benzimidazole N-Oxides Unsubstituted at N-1 and C-2

Harvey, Ian W.,McFarlane, Michael D.,Moody, David J.,Smith, David M.

, p. 681 - 690 (2007/10/02)

Since previous routes to the title compounds (1) have proved unsatisfactory as general methods, a simple new synthesis has been devised.N-Cyanomethyl-o-nitroanilines (5) are cyclised in basic media, giving 2-cyanobenzimidazole N-oxides (12) in good yield.Hydrolysis of these products with hydrochloric acid gives, directly, the title compounds as their hydrochloride salts (13), which may be isolated and purified, and which give the free N-oxides (1) by treatment with aqueous ammonia followed by evaporation. o-Nitrophenylglycine esters (4) may satisfactorily replace the nitriles (5) in certain cases.A modification of this kind in the related nitropyridylglycine series leads to 3H-imidazolpyridine 1-oxide (20).

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