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Cyclotriacotane is a hypothetical cyclic alkane with the molecular formula C39H78, consisting of 39 carbon atoms and 78 hydrogen atoms arranged in a triangular cyclic structure. It is a member of the acotane family, which are large cyclic alkanes with 3n carbon atoms, where n is an integer. Cyclotriacotane is not commonly found in nature and has not been synthesized yet, making it a purely theoretical compound. Its properties, such as boiling point, melting point, and reactivity, are not well-defined due to its hypothetical nature. However, it is expected to exhibit similar characteristics to other cyclic alkanes, such as high stability and low reactivity due to the absence of functional groups.

297-35-8

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297-35-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 297-35-8 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 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 297-35:
(5*2)+(4*9)+(3*7)+(2*3)+(1*5)=78
78 % 10 = 8
So 297-35-8 is a valid CAS Registry Number.
InChI:InChI=1/C30H60/c1-2-4-6-8-10-12-14-16-18-20-22-24-26-28-30-29-27-25-23-21-19-17-15-13-11-9-7-5-3-1/h1-30H2

297-35-8SDS

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 Cyclotriacontane

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:297-35-8 SDS

297-35-8Downstream Products

297-35-8Relevant 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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