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2-(5-bromo-2-hydroxyphenyl)-1,3-dioxane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 923571-63-5 Structure
  • Basic information

    1. Product Name: 2-(5-bromo-2-hydroxyphenyl)-1,3-dioxane
    2. Synonyms: 2-(5-bromo-2-hydroxyphenyl)-1,3-dioxane
    3. CAS NO:923571-63-5
    4. Molecular Formula:
    5. Molecular Weight: 259.1
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 923571-63-5.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-(5-bromo-2-hydroxyphenyl)-1,3-dioxane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(5-bromo-2-hydroxyphenyl)-1,3-dioxane(923571-63-5)
    11. EPA Substance Registry System: 2-(5-bromo-2-hydroxyphenyl)-1,3-dioxane(923571-63-5)
  • 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: 923571-63-5(Hazardous Substances Data)

923571-63-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 923571-63-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,3,5,7 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 923571-63:
(8*9)+(7*2)+(6*3)+(5*5)+(4*7)+(3*1)+(2*6)+(1*3)=175
175 % 10 = 5
So 923571-63-5 is a valid CAS Registry Number.

923571-63-5Relevant articles and documents

Metal-salen-base-pair complexes inside DNA: Complexation overrides sequence information

Clever, Guido H.,Soeltl, Yvonne,Burks, Heather,Spahl, Werner,Carell, Thomas

, p. 8708 - 8718 (2006)

Two isomeric salicylic alde-hyde nucleobases have been prepared and incorporated into various DNA duplexes. Reaction with ethylenediamine leads to formation of the well-known salen ligand inside the DNA double helix. Addition of transition-metal ions such as Cu2+, Mn2+, Ni 2+, Fe2+, or VO2+ results in the formation of metal-salen-base-pair complexes, which were studied by using UV and circular dichroism (CD) spectroscopy. HPLC and ESI mass spectrometric measurements reveal an unusually high stability of the DNA-metal system. These metal-salen complexes act as interstrand cross-links and thereby lead to a strong stabilization of the DNA duplexes, as studied by thermal de- and renaturing experiments. Complex formation is strong enough to override sequence information even when the preorganization of the ligand precursors is unfavorable and the DNA duplex is distorted by the metal complexation. Furthermore, melting-point studies show that the salen complex derived from ligand 2 fits better into the DNA duplex, in accordance with results obtained from the crystal structure of the corresponding copper-salen complex 8.

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