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Cyclohexane, (2-propynyloxy)-, also known as 2-propynoxy-cyclohexane, is a colorless liquid chemical compound with the molecular formula C9H14O. It has a slightly sweet odor and is commonly used as a solvent in various industrial applications due to its unique properties.

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  • 67967-07-1 Structure
  • Basic information

    1. Product Name: Cyclohexane, (2-propynyloxy)-
    2. Synonyms:
    3. CAS NO:67967-07-1
    4. Molecular Formula: C9H14O
    5. Molecular Weight: 138.21
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 67967-07-1.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: Cyclohexane, (2-propynyloxy)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cyclohexane, (2-propynyloxy)-(67967-07-1)
    11. EPA Substance Registry System: Cyclohexane, (2-propynyloxy)-(67967-07-1)
  • 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: 67967-07-1(Hazardous Substances Data)

67967-07-1 Usage

Uses

Used in Adhesives Industry:
Cyclohexane, (2-propynyloxy)is used as a solvent in the production of adhesives for its ability to dissolve and mix with various components, enhancing the adhesive's performance and bonding capabilities.
Used in Coatings Industry:
In the coatings industry, Cyclohexane, (2-propynyloxy)is utilized as a solvent to improve the flow and application properties of coatings, ensuring a smooth and even finish.
Used in Resins Industry:
Cyclohexane, (2-propynyloxy)is used as a solvent in the production of resins, aiding in the process of dissolving and combining raw materials to create a uniform end product.
Used as a Stabilizer in Polymer and Plastics Manufacturing:
Cyclohexane, (2-propynyloxy)is employed as a stabilizer in the manufacturing of polymers and plastics to prevent degradation and maintain the material's properties during processing and use.
Precautions:
Due to its potential flammability and toxicity, proper handling and storage precautions should be taken when working with Cyclohexane, (2-propynyloxy)to ensure safety and minimize environmental impact.

Check Digit Verification of cas no

The CAS Registry Mumber 67967-07-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,9,6 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 67967-07:
(7*6)+(6*7)+(5*9)+(4*6)+(3*7)+(2*0)+(1*7)=181
181 % 10 = 1
So 67967-07-1 is a valid CAS Registry Number.

67967-07-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name prop-2-ynoxycyclohexane

1.2 Other means of identification

Product number -
Other names cyclohexyl propargyl ether

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:67967-07-1 SDS

67967-07-1Relevant articles and documents

The palladium catalyzed asymmetric addition of oxindoles and allenes: An atom-economical versatile method for the construction of chiral indole alkaloids

Trost, Barry M.,Xie, Jia,Sieber, Joshua D.

supporting information; experimental part, p. 20611 - 20622 (2012/02/01)

The Pd-catalyzed asymmetric allylic alkylation (AAA) is one of the most useful and versatile methods for asymmetric synthesis known in organometallic chemistry. Development of this reaction over the past 30 years has typically relied on the use of an ally

Total synthesis of (±)-magnofargesin

Wardrop, Duncan J.,Fritz, Joseph

, p. 3659 - 3662 (2007/10/03)

A convenient method for the preparation of 2,5-dihydrofurans by using the chemistry of alkynyl(phenyl)iodonium salts is reported. Treatment of 3-alkoxy-1-alkynyl(phenyl)iodonium triflates with sodium benzenesulfinate generates an alkylidenecarbene, which

Reductive free-radical alkylations and cyclisations mediated by 1-alkylcyclohexa-2,5-diene-1-carboxylic acids

Baguley, Paul A.,Walton, John C.

, p. 2073 - 2082 (2007/10/03)

A range of 1-alkylcyclohexa-2,5-diene-1-carboxylic acids were prepared by Birch reduction-alkylation of benzoic acid and their efficiency as mediators of alkyl radical chain addition and cyclisation processes was investigated. Reductive alkylations were respectably successful, even with only one or two equivalents of alkene, for secondary, tertiary and benzylic radicals. Reaction of 1-[2-(cyclohex-2-enyloxy)ethyl]cyclohexa-2,5-diene-1-carboxylic acid yielded the product of exo-trig-cyclisation, i.e. 7-oxabicyclo[4.3.0]nonane, in a yield comparable to that obtained from the tributyltin hydride induced cyclisation of 3-(2′-iodoethoxy)-cyclohexene. This, together with the isolation of both exo- and endo-cyclisation products from 1-[2-(6,6-dimethylbicyclo[3.1.1]hept-2-en-2-ylmethoxy)ethyl]cyclohexa-2,5-diene- 1-carboxylic acid established that ring closures could also be satisfactorily mediated with these reagents. Preparations were completely free of metal contaminants and direct reduction of the alkyl radicals, prior to addition or cyclisation, was completely absent. However, the desired products were accompanied by alkylbenzenes, together with by-products from the initiator decompositions, and this complicated work-up. Failure to obtain 1-[2-(prop-2-yn-1-yloxy)cyclohexyl]cyclohexa-2,5-diene-1-carboxylic acid in Birch reductive alkylations with trans-1-iodo-2-(prop-2-yn-1-yloxy)cyclohexane (and the corresponding bromide) indicated a limitation on precursor synthesis. The Birch reduction-alkylation was not of universal applicability and was suppressed for alkyl halides having β-substituents.

A Convenient Procedure for the Synthesis of Propargyl Ethers Derived from Secondary Alcohols

Almansa, Carme,Moyano, Albert,Pericas, Miquel A.,Serratosa, Felix

, p. 707 - 709 (2007/10/02)

A new and efficient two-step synthesis of propargyl ethers derived from secondary alcohols, involving the formation of 1-propynyl ethers followed by isomerization with potassium 3-aminopropylamide, is described.The process is insensitive to the steric hin

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