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CAS

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76015-03-7

1-(1-Ethynyl-pentyl)-cyclohexanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 76015-03-7 Structure

  • Basic information

    1. Product Name: 1-(1-Ethynyl-pentyl)-cyclohexanol
    2. Synonyms:
    3. CAS NO:76015-03-7
    4. Molecular Formula:
    5. Molecular Weight: 194.317
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 76015-03-7.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: 1-(1-Ethynyl-pentyl)-cyclohexanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(1-Ethynyl-pentyl)-cyclohexanol(76015-03-7)
    11. EPA Substance Registry System: 1-(1-Ethynyl-pentyl)-cyclohexanol(76015-03-7)

  • 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: 76015-03-7(Hazardous Substances Data)

76015-03-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76015-03-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,0,1 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 76015-03:
(7*7)+(6*6)+(5*0)+(4*1)+(3*5)+(2*0)+(1*3)=107
107 % 10 = 7
So 76015-03-7 is a valid CAS Registry Number.

76015-03-7Downstream Products

76015-03-7Relevant articles and documents

Chain-extension Reactions of Acetylenes. Part 4. Reaction of 1,3-Dilithioacetylides with Carbonyl Electrophiles, Hexamethylphosphoric Triamide, and Benzylideneaniline

Pover, Keith A.,Scheinmann, Feodor

, p. 2338 - 2345 (2007/10/02)

The regioselectivity of the reactions of 1,3-dilithioalk-1-ynes with various electrophiles has been examined.With formaldehyde and cyclic ketones, reaction occur at C-1 and C-3 to give alk-2-yne-1,5-diols.In contrast reactions with carbon dioxide give allene-1,3-dicarboxylic acids. 1,3-Dilithioalk-1-ynes decompose hexamethylphosphoric triamide and the resulting N-methylmethyleneamine undergoes addition only at the propargylic site.Further reaction with either 1-bromobutane or water gives alkynylamines.Benzylideneaniline also reacts with 1,3-dilithiohex- and hept-1-ynes only at the propargylic site to give N-phenylbut-3-ynylamines.

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