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119438-03-8

DCM-H is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 119438-03-8 Structure

  • Basic information

    1. Product Name: DCM-H
    2. Synonyms: DCM-H
    3. CAS NO:119438-03-8
    4. Molecular Formula:
    5. Molecular Weight: 260.295
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 119438-03-8.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: DCM-H(CAS DataBase Reference)
    10. NIST Chemistry Reference: DCM-H(119438-03-8)
    11. EPA Substance Registry System: DCM-H(119438-03-8)

  • 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: 119438-03-8(Hazardous Substances Data)

119438-03-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119438-03-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,4,3 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 119438-03:
(8*1)+(7*1)+(6*9)+(5*4)+(4*3)+(3*8)+(2*0)+(1*3)=128
128 % 10 = 8
So 119438-03-8 is a valid CAS Registry Number.

119438-03-8Downstream Products

119438-03-8Relevant articles and documents

Ion-Responsive Fluorescent Compounds, 2. Cation-Steered Intramolecular Charge Transfer in a Crowned Merocyanine

Bourson, Jean,Valeur, Bernard

, p. 3871 - 3876 (2007/10/02)

The dimethylamine group of DCM (4-dicyanomethylene-2-methyl-6--4H-pyran), a well-known merocyanine often used as a laser dye, has been replaced by a macrocycle (monoaza-15-crown-5) which acts also as an electron donating substituent.The resulting fluoroionophore (DCM-crown) has almost identical photophysical properties as DCM, but upon complexation by alkaline-earth-metal-cations, it undergoes drastic changes in absorption spectrum (hypsochromic shift and hypochromic effect) and fluorescence quantum yield (quenching), whereas the emission spectrum is only slightly blue-shifted and the fluorescence lifetime is almost unchanged.These effects which strongly depend on the charge density of the cation can be interpreted in terms of cation-steered reduction of the efficiency of tranfer from a nonemissive locally excited state to an emissive relaxed intramolecular charge-transfer state (RICT).

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