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CAS

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13151-55-8

ethylcycloheptane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 13151-55-8 Structure

  • Basic information

    1. Product Name: ethylcycloheptane
    2. Synonyms: cycloheptane, ethyl-; Ethylcycloheptane
    3. CAS NO:13151-55-8
    4. Molecular Formula: C9H18
    5. Molecular Weight: 126.2392
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 13151-55-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 160.1°C at 760 mmHg
    3. Flash Point: 36.8°C
    4. Appearance: N/A
    5. Density: 0.78g/cm3
    6. Vapor Pressure: 3.15mmHg at 25°C
    7. Refractive Index: 1.427
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: ethylcycloheptane(CAS DataBase Reference)
    11. NIST Chemistry Reference: ethylcycloheptane(13151-55-8)
    12. EPA Substance Registry System: ethylcycloheptane(13151-55-8)

  • 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: 13151-55-8(Hazardous Substances Data)

13151-55-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13151-55-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,5 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13151-55:
(7*1)+(6*3)+(5*1)+(4*5)+(3*1)+(2*5)+(1*5)=68
68 % 10 = 8
So 13151-55-8 is a valid CAS Registry Number.

13151-55-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ethylcycloheptane

1.2 Other means of identification

Product number -
Other names Aethyl-cycloheptan

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:13151-55-8 SDS

13151-55-8Relevant articles and documents

Thermal C-H Activation Catalyzed by RhCl(CH2=CH2)(PMe3)2. Hydrogen Transfer from Cycloalkanes to Ethylene and Ethylene Insertion into Cycloalkanes

Sakakura, Toshiyasu,Tanaka, Masato

, p. 359 - 362 (2007/10/02)

Dehydrogenation of cycloalkanes to cycloalkenes is catalyzed by RhCl(CH2=CH2)(PMe3)2 under ethylene pressure at a high temperature over 170 deg C.Ethylene insertion into sp3 C-H bond of cycloalkanes occurs at 230 deg C to afford ethylcycloalkanes.

SYNTHESIS AND THERMAL TRANSFORMATIONS OF BICYCLOALKENES CONTAINING A METHYLENECYCLOPROPANE FRAGMENT

Mil'vitskaya, E. M.,Pekhk, T. I.,Pereslegina, N. S.,Tarakanova, A. V.,Ivanov, A. V.

, p. 1573 - 1583 (2007/10/02)

The previously undescribed 8-methylenebicyclooct-2-ene (II) and 9-methylenebicyclonon-4-ene (IV) were synthesized by the dehydrohalogenation of 8-methyl-8-chlorobicyclooct-2-ene and 9-methyl-9-chlorobicyclonon-4-ene.It was established that the hydrocarbon (II) is thermally labile, whereas the hydrocarbon (IV) does not change right up to 300 deg C.The thermal transformations of the hydrocarbon (II) and its isomeric bicyclonona-1,6-diene (III) at 100 - 180 deg C were investigated.At 100 deg C a pseudoequilibrium is established between these hydrocarbons.The final and only products from the transformations of both hydrocarbons at 180 deg C are the previously unknown anti-Bredt hydrocarbon bicyclonona-2,7-diene (XXVIIIb) and 3-methylene-1,4-cyclooctadiene (XXV), formed in a ratio of 1 : 2.5.

Hydrogenolysis of Small Cycloalkanes, X. - Catalytic Hydrogenation of Bicycloalkanes

Stahl, Karl-Johannes,Hertzsch, Winfried,Musso, Hans

, p. 1474 - 1484 (2007/10/02)

Dependent on n different products are obtained from bicycloalkanes by hydrogenation on Pt and Pd/C catalysts: from n = 5 onward only methylcycloalkanes of the same ring size; with n = 4 additionally 2-7 percent of cycloheptane is formed; with n = 3 ring enlargement increases to 5-20 percent and with n = 2 cyclopentane is the only product.Mainly butane is formed from bicyclobutane and no intermediate could be detected.Explanations are attempted.The expected products are produced on hydrogenation of methyl-substituted derivatives and spiroalkanes.

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