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N-(2-methyl-6-nitrophenyl)glycine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 191847-67-3 Structure
  • Basic information

    1. Product Name: N-(2-methyl-6-nitrophenyl)glycine
    2. Synonyms: N-(2-methyl-6-nitrophenyl)glycine
    3. CAS NO:191847-67-3
    4. Molecular Formula:
    5. Molecular Weight: 210.189
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 191847-67-3.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: N-(2-methyl-6-nitrophenyl)glycine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(2-methyl-6-nitrophenyl)glycine(191847-67-3)
    11. EPA Substance Registry System: N-(2-methyl-6-nitrophenyl)glycine(191847-67-3)
  • 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: 191847-67-3(Hazardous Substances Data)

191847-67-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 191847-67-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,8,4 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 191847-67:
(8*1)+(7*9)+(6*1)+(5*8)+(4*4)+(3*7)+(2*6)+(1*7)=173
173 % 10 = 3
So 191847-67-3 is a valid CAS Registry Number.

191847-67-3Relevant articles and documents

O-Nitroaniline derivatives. Part 14. Cyclisations leading to benzimidazole N-oxides, N-hydroxybenzimidazolones and N-hydroxyquinoxaline-2,3-diones: A mechanistic borderline

Collins Cafiero, Pamela A.,French, Colin S.,McFarlane, Michael D.,Mackie, Raymond K.,Smith, David M.

, p. 1375 - 1384 (2007/10/03)

The base-induced cyclisations of N-(o-nitrophenyl)glycine derivatives (nitriles 9 or esters 13) bearing additional substituents at the other ortho-position are anomalous, resembling those involving N-(o-nitrophenyl)sarcosine analogues. The nitriles are co

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