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179264-44-9

4,4''-(2,5-DIBUTOXY-1,4-PHENYLENE)BIS[2-METHYL-3-BUTYN-2-OL] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 179264-44-9 Structure

  • Basic information

    1. Product Name: 4,4''-(2,5-DIBUTOXY-1,4-PHENYLENE)BIS[2-METHYL-3-BUTYN-2-OL]
    2. Synonyms: 4,4''-(2,5-DIBUTOXY-1,4-PHENYLENE)BIS[2-METHYL-3-BUTYN-2-OL]
    3. CAS NO:179264-44-9
    4. Molecular Formula: C24H34O4
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 179264-44-9.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: 4,4''-(2,5-DIBUTOXY-1,4-PHENYLENE)BIS[2-METHYL-3-BUTYN-2-OL](CAS DataBase Reference)
    10. NIST Chemistry Reference: 4,4''-(2,5-DIBUTOXY-1,4-PHENYLENE)BIS[2-METHYL-3-BUTYN-2-OL](179264-44-9)
    11. EPA Substance Registry System: 4,4''-(2,5-DIBUTOXY-1,4-PHENYLENE)BIS[2-METHYL-3-BUTYN-2-OL](179264-44-9)

  • 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: 179264-44-9(Hazardous Substances Data)

179264-44-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 179264-44-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,2,6 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 179264-44:
(8*1)+(7*7)+(6*9)+(5*2)+(4*6)+(3*4)+(2*4)+(1*4)=169
169 % 10 = 9
So 179264-44-9 is a valid CAS Registry Number.

179264-44-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[2,5-dibutoxy-4-(3-hydroxy-3-methylbut-1-ynyl)phenyl]-2-methylbut-3-yn-2-ol

1.2 Other means of identification

Product number -
Other names InChI=1/C24H34O4/c1-7-9-15-27-21-17-20(12-14-24(5,6)26)22(28-16-10-8-2)18-19(21)11-13-23(3,4)25/h17-18,25-26H,7-10,15-16H2,1-6H

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:179264-44-9 SDS

179264-44-9Relevant articles and documents

Terpyridine-platinum(ii) acetylide complexes bearing pendent coordination units

Ziessel, Raymond,Diring, Stephane,Retailleau, Pascal

, p. 3285 - 3290 (2007/10/03)

Platinum(ii) complexes bearing various alkyne-pyrene, alkyne-4′-terpyridine and alkyne-dibutoxyphenylacetylide-terpyridine units were constructed in a step-by-step procedure based on copper-promoted cross-coupling reactions with preconstructed modules; formation of bis(ligand) complexes of Fe(ii) and Zn(ii) by binding of the pendent terpyridine units provided heterotrinuclear derivatives, all of which exhibit highly structured absorption features in solution and display a rich electrochemistry due to the presence of various redox active modules. The Royal Society of Chemistry 2006.

The preparation and some properties of substituted phenylene-ethynylene and phenylenebuta-1,3-diynylene polymers

Pelter, Andrew,Jones, D. Elfyn

, p. 2289 - 2294 (2007/10/03)

Syntheses are described for the preparation of a variety of diynes which are converted to high molecular weight substituted arylenebuta-1,3-diynylene polymers by oxidative coupling and to high molecular weight substituted arylene-ethynylene polymers by Pd(II) catalysed cross coupling reactions. The products tend to be insoluble in normal organic solvents. Doping with ferric chloride produces significant changes in conductivity but these are less than those produced on equivalently substituted thienylene-phenylene polymers.

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