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Benzene, 1-bromo-4-ethynyl-2,5-dihexyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 194015-34-4 Structure
  • Basic information

    1. Product Name: Benzene, 1-bromo-4-ethynyl-2,5-dihexyl-
    2. Synonyms:
    3. CAS NO:194015-34-4
    4. Molecular Formula: C20H29Br
    5. Molecular Weight: 349.354
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 194015-34-4.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: Benzene, 1-bromo-4-ethynyl-2,5-dihexyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzene, 1-bromo-4-ethynyl-2,5-dihexyl-(194015-34-4)
    11. EPA Substance Registry System: Benzene, 1-bromo-4-ethynyl-2,5-dihexyl-(194015-34-4)
  • 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: 194015-34-4(Hazardous Substances Data)

194015-34-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 194015-34-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,0,1 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 194015-34:
(8*1)+(7*9)+(6*4)+(5*0)+(4*1)+(3*5)+(2*3)+(1*4)=124
124 % 10 = 4
So 194015-34-4 is a valid CAS Registry Number.

194015-34-4Relevant articles and documents

Synthesis and Characterization of Monodisperse Oligo(phenyleneethynylene)s

Ziener, Ulrich,Godt, Adelheid

, p. 6137 - 6143 (2007/10/03)

An iterative convergent/divergent synthesis for hexyl- and isopentoxy-substituted, monodisperse oligo(phenyleneethynylene)s is reported. The strategy is based on the bromine-iodine selectivity of the Pd-catalyzed alkyne-aryl-coupling, the conversion of a bromine substituent into an iodine substituent via halogen metal exchange, and trimethylsilyl (TMS) as an acetylene protecting group. The synthesis is efficient and gave gram amounts of octamers. Further derivatization of the octamers to esters and carboxylic acids is described. The compounds are fully characterized by 1H and 13C NMR and UV/vis spectroscopy.

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