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N-(2-aminophenyl)-N-methylacetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 22902-29-0 Structure
  • Basic information

    1. Product Name: N-(2-aminophenyl)-N-methylacetamide
    2. Synonyms: N-(2-aminophenyl)-N-methylacetamide
    3. CAS NO:22902-29-0
    4. Molecular Formula: C9H12N2O
    5. Molecular Weight: 164.207
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 22902-29-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: N-(2-aminophenyl)-N-methylacetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(2-aminophenyl)-N-methylacetamide(22902-29-0)
    11. EPA Substance Registry System: N-(2-aminophenyl)-N-methylacetamide(22902-29-0)
  • 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: 22902-29-0(Hazardous Substances Data)

22902-29-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22902-29-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,9,0 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 22902-29:
(7*2)+(6*2)+(5*9)+(4*0)+(3*2)+(2*2)+(1*9)=90
90 % 10 = 0
So 22902-29-0 is a valid CAS Registry Number.

22902-29-0Downstream Products

22902-29-0Relevant articles and documents

Trapping of translocated radicals by tetrathiafulvalene radical cation

Murphy, John A.,Roome, Stephen J.

, p. 1349 - 1358 (2007/10/02)

Aryl radicals are generated by electron transfer from tetrathiafulvalene to arenediazonium salts.The aryl radicals are translocated into alkyl radicals which undergo a C-S or C-C bond formation to tetrathiafulvalene radical cation, depending on the nucleophilicity/electrophilicity of the translocated carbon radical.

Process for extracting cobalt, copper or zinc values using a 1-alkyl substituted benzimidazole

-

, (2008/06/13)

Optionally substituted benzimidazoles containing an alkyl or cycloalkyl group in position 1 and containing at least 5 alkyl or cycloalkyl carbon atoms extract metals from aqueous solutions of their salts into water-immiscible organic solvents in presence

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