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CAS

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297-54-1

Cyclotetracontane, also known as tetracontane, is a cyclic alkane with the molecular formula C36H72. It is a member of the cycloalkane family, which consists of saturated hydrocarbons with a closed ring structure. Cyclotetracontane is composed of 36 carbon atoms and 72 hydrogen atoms, arranged in a single, continuous chain that forms a closed loop. This large cyclic molecule is relatively rare and not commonly found in nature, but it can be synthesized in the laboratory. Due to its size and complexity, cyclotetracontane has unique physical and chemical properties, such as high melting and boiling points, low reactivity, and limited solubility in water. It is primarily of interest to researchers studying the properties of large cyclic hydrocarbons and their potential applications in various fields, including materials science and organic chemistry.

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  • 297-54-1 Structure

  • Basic information

    1. Product Name: Cyclotetracontane
    2. Synonyms: Cyclotetracontane
    3. CAS NO:297-54-1
    4. Molecular Formula: C40H80
    5. Molecular Weight: 561.075
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 297-54-1.mol

  • Chemical Properties

    1. Melting Point: 82-84 °C
    2. Boiling Point: 652.5±22.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: 0.790±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Cyclotetracontane(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cyclotetracontane(297-54-1)
    11. EPA Substance Registry System: Cyclotetracontane(297-54-1)

  • 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: 297-54-1(Hazardous Substances Data)

297-54-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 297-54-1 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, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 297-54:
(5*2)+(4*9)+(3*7)+(2*5)+(1*4)=81
81 % 10 = 1
So 297-54-1 is a valid CAS Registry Number.

297-54-1SDS

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 Cyclotetracontan

1.2 Other means of identification

Product number -
Other names cyclotetracontane

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:297-54-1 SDS

297-54-1Downstream Products

297-54-1Relevant articles and documents

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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