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2-Pyridinamine,N-ethyl-N-2-pyridinyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 622408-77-9 Structure
  • Basic information

    1. Product Name: 2-Pyridinamine,N-ethyl-N-2-pyridinyl-(9CI)
    2. Synonyms: 2-Pyridinamine,N-ethyl-N-2-pyridinyl-(9CI)
    3. CAS NO:622408-77-9
    4. Molecular Formula: C12H13N3
    5. Molecular Weight: 199.25172
    6. EINECS: N/A
    7. Product Categories: PYRIDINE
    8. Mol File: 622408-77-9.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: 2-Pyridinamine,N-ethyl-N-2-pyridinyl-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Pyridinamine,N-ethyl-N-2-pyridinyl-(9CI)(622408-77-9)
    11. EPA Substance Registry System: 2-Pyridinamine,N-ethyl-N-2-pyridinyl-(9CI)(622408-77-9)
  • 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: 622408-77-9(Hazardous Substances Data)

622408-77-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 622408-77-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,2,4,0 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 622408-77:
(8*6)+(7*2)+(6*2)+(5*4)+(4*0)+(3*8)+(2*7)+(1*7)=139
139 % 10 = 9
So 622408-77-9 is a valid CAS Registry Number.

622408-77-9Downstream Products

622408-77-9Relevant articles and documents

Kinetic and mechanistic studies of cisplatin analogues bearing 2,2′-dipyridylalkylamine ligands

Kinunda, Grace,Jaganyi, Deogratius

, p. 235 - 248 (2016)

A series of mononuclear Pt(II) complexes of the type diaqua(2,2′-dipyridylalkylamine)platinum(II) (where the alkyl group = methyl, ethyl, propyl, butyl or hexyl) were synthesized to investigate their nucleophilic substitution behaviour and the influence of the alkyl chain bonded to the tertiary nitrogen atom joining the two pyridine rings on the reactivity of the chosen complexes. The trend in rate constant shows that introduction of the σ-donating alkyl chain on the tertiary nitrogen joining the two pyridine moieties reduces the π-acceptor ability of the cis coordinated pyridine rings resulting in a less reactive Pt(II) centre which causes a decrease in the reaction rate. This is well supported by data from DFT calculations. It is also evident that the alkyl chain also introduces a steric effect which blocks the approach of the nucleophile to the Pt(II) centre. The boat-like structure of the six-membered chelate ring also contributes to the steric effect. The study has also shown that two substitution processes going through an associative mode of activation are observed. The first is the simultaneous substitution of the two aqua ligands, and the second is due to the dechelation of the ligand, an indication of possible disintegration of the complex if used as a drug. Graphical Abstract: The substitution reactions of cisplatin analogues and bio-relevant thiourea nucleophiles follow two-step associative processes with the last step encountering a complete dechelation of the ligand.[Figure not available: see fulltext.]

METALLOINSERTOR COMPLEXES TARGETED TO DNA MISMATCHES

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Paragraph 00147-00148, (2015/01/09)

A composition including a Rh or Ru metailoinsertor complex specifically targets mismatch repair (MMR)~deficient cells. Selective cytotoxicity is induced in MMR-deficient cells upon uptake of the inventive metailoinsertor complexes.

METALLOINSERTOR COMPLEXES TARGETED TO DNA MISMATCHES

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Page/Page column 20, (2012/12/13)

A composition including a Rh or Ru metalloinsertor complex specifically targets mismatch repair (MMR)-deficient cells. Selective cytotoxicity is induced in MMR-deficient cells upon uptake of the inventive metalloinsertor complexes.

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