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1,3,5,7-Cyclooctatetraene, 1,2,4,7-tetramethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17340-07-7

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17340-07-7 Usage

Explanation

The compound is composed of 12 carbon atoms and 16 hydrogen atoms.

Explanation

The carbon atoms are arranged in a closed loop, forming an eight-membered ring.

Explanation

The eight-membered ring has four methyl groups (CH3) attached to specific carbon atoms.

Explanation

The methyl groups are attached to the first, second, fourth, and seventh carbon atoms of the ring.

Explanation

Despite having a cyclic structure, the compound does not exhibit aromaticity due to the presence of four methyl groups, which disrupt the necessary delocalization of electrons for aromaticity.

Explanation

The compound can participate in a range of chemical reactions, making it useful in organic synthesis and as a building block for more complex molecules.

Explanation

It is used in the synthesis of other organic compounds and as a reagent in research and academic laboratories for chemical experiments and studies.

Explanation

The presence of the four methyl groups makes the compound less stable compared to other cyclic hydrocarbons without such substituents.

Explanation

Based on its molecular weight and structure, the compound is expected to be a liquid or solid at room temperature, although specific data on its physical state is not provided.

Explanation

As a hydrocarbon, the compound is likely to be soluble in nonpolar organic solvents such as hexane, toluene, or chloroform.

Structure

Cyclic hydrocarbon with an eight-membered ring

Substituents

Four methyl groups

Position of Methyl Groups

1, 2, 4, and 7

Aromaticity

Non-aromatic

Chemical Reactivity

Capable of undergoing various reactions

Applications

Organic synthesis and research

Stability

Less stable than some other cyclic hydrocarbons

Physical State

Likely a liquid or solid at room temperature

Solubility

Soluble in organic solvents

Check Digit Verification of cas no

The CAS Registry Mumber 17340-07-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,4 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17340-07:
(7*1)+(6*7)+(5*3)+(4*4)+(3*0)+(2*0)+(1*7)=87
87 % 10 = 7
So 17340-07-7 is a valid CAS Registry Number.

17340-07-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,6,8-tetramethylcycloocta-1,3,5,7-tetraene

1.2 Other means of identification

Product number -
Other names 1,2,4,7-Tetramethyl-cyclooctatetraen

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:17340-07-7 SDS

17340-07-7Downstream Products

17340-07-7Relevant academic research and scientific papers

COOLIGOMERIZATION OF PROPADIENE WITH PROPYNE CATALYSED BY NICKEL(0) COMPLEXES

Cermak, Jan,Blechta, Vratislav,Chvalovsky, Vaclav

, p. 1274 - 1286 (2007/10/02)

Cooligomerization of propadiene with propyne catalysed by bis(1,5-cyclooctadiene)nickel and tetrakis(triphenylphosphine)nickel gives a variety of products, including besides the cooligomers also the homooligomers of both monomers.The type of catalyst affects partially the product distribution due to changes in the degree of oligomerization.Cooligomerization of propadiene with 3-deuteriopropyne provided information about relative proportion of propadiene and propyne units in the oligomers.

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