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Cycloheptadecane is a cyclic alkane with the molecular formula C17H34, consisting of 17 carbon atoms arranged in a closed ring structure. It is a member of the cycloalkane family, which are saturated hydrocarbons with a cyclic arrangement of carbon atoms. Cycloheptadecane is a colorless, odorless, and non-polar liquid at room temperature, with a low solubility in water. It is relatively stable and unreactive due to its saturated nature, making it resistant to oxidation and other chemical reactions. Cycloheptadecane is primarily used as a solvent, a component in various chemical formulations, and as a precursor in the synthesis of other organic compounds. Cycloheptadecane's unique cyclic structure and properties make it an interesting subject for study in organic chemistry and industrial applications.

295-97-6

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295-97-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 295-97-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,9 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 295-97:
(5*2)+(4*9)+(3*5)+(2*9)+(1*7)=86
86 % 10 = 6
So 295-97-6 is a valid CAS Registry Number.

295-97-6SDS

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 cycloheptadecane

1.2 Other means of identification

Product number -
Other names -

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

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More Details:295-97-6 SDS

295-97-6Upstream product

295-97-6Downstream Products

295-97-6Relevant academic research and scientific papers

Cyclooctane metathesis catalyzed by silica-supported tungsten pentamethyl [(ΞSiO)W(Me)5]: Distribution of macrocyclic alkanes

Riache, Nassima,Callens, Emmanuel,Samantaray, Manoja K.,Kharbatia, Najeh M.,Atiqullah, Muhammad,Basset, Jean-Marie

supporting information, p. 15089 - 15094 (2015/02/19)

Metathesis of cyclic alkanes catalyzed by the new surface complex [(ΞSiO)W(Me)5] affords a wide distribution of cyclic and macrocyclic alkanes. The major products with the formula CnH2n are the result of either a ring contraction or ring expans

Catalytic ring expansion, contraction, and metathesis-polymerization of cycloalkanes

Ahuja, Ritu,Kundu, Sabuj,Goldman, Alan S.,Brookhart, Maurice,Vicente, Brian C.,Scott, Susannah L.

, p. 253 - 255 (2008/03/13)

Tandem dehydrogenation-olefin-metathesis catalyst systems, comprising a pincer-ligated iridium-based alkane dehydrogenation catalyst and a molybdenum-based olefin-metathesis catalyst, are reported to effect the metathesis-cyclooligomerization of cyclooctane and cyclodecane to give cycloalkanes with various carbon numbers, predominantly multiples of the substrate carbon number, and polymers. The Royal Society of Chemistry.

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