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102308-59-8

2-((2-methyl-4-nitrophenyl)amino)acetic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 102308-59-8 Structure

  • Basic information

    1. Product Name: 2-((2-methyl-4-nitrophenyl)amino)acetic acid
    2. Synonyms: 2-((2-methyl-4-nitrophenyl)amino)acetic acid
    3. CAS NO:102308-59-8
    4. Molecular Formula:
    5. Molecular Weight: 210.189
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 102308-59-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-((2-methyl-4-nitrophenyl)amino)acetic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-((2-methyl-4-nitrophenyl)amino)acetic acid(102308-59-8)
    11. EPA Substance Registry System: 2-((2-methyl-4-nitrophenyl)amino)acetic acid(102308-59-8)

  • 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: 102308-59-8(Hazardous Substances Data)

102308-59-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102308-59-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,3,0 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 102308-59:
(8*1)+(7*0)+(6*2)+(5*3)+(4*0)+(3*8)+(2*5)+(1*9)=78
78 % 10 = 8
So 102308-59-8 is a valid CAS Registry Number.

102308-59-8Relevant articles and documents

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 [

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