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CAS

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79392-44-2

3-[(2-ethylhexyl)disulfanyl]methylheptane is a complex organic compound that consists of sulfur, carbon, and hydrogen atoms. It features an alkyl disulfide group connected to a heptane backbone, with the alkyl disulfide section including a 2-ethylhexyl component. Although there are no specific known uses or applications for this compound in current scientific research or industrial fields, the intricacy of its structure may hold potential for future chemical studies and possible utilization in chemical reactions due to its diverse atomic composition.

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  • 79392-44-2 Structure

  • Basic information

    1. Product Name: 3-{[(2-ethylhexyl)disulfanyl]methyl}heptane
    2. Synonyms:
    3. CAS NO:79392-44-2
    4. Molecular Formula: C16H34S2
    5. Molecular Weight: 290.5712
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 79392-44-2.mol
    9. Article Data: 1

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 361°C at 760 mmHg
    3. Flash Point: 102.4°C
    4. Appearance: N/A
    5. Density: 0.904g/cm3
    6. Vapor Pressure: 4.44E-05mmHg at 25°C
    7. Refractive Index: 1.484
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 3-{[(2-ethylhexyl)disulfanyl]methyl}heptane(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-{[(2-ethylhexyl)disulfanyl]methyl}heptane(79392-44-2)
    12. EPA Substance Registry System: 3-{[(2-ethylhexyl)disulfanyl]methyl}heptane(79392-44-2)

  • 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: 79392-44-2(Hazardous Substances Data)

79392-44-2 Usage

Uses

Currently, there are no specific applications or industries where 3-[(2-ethylhexyl)disulfanyl]methylheptane is known to be used. However, given its unique structure and the presence of various elements, it may be of interest for future research and development in the chemical industry. Potential applications could include:
Used in Chemical Research:
3-[(2-ethylhexyl)disulfanyl]methylheptane could be used as a subject of study for understanding its chemical properties and reactivity, potentially leading to the discovery of new applications or reactions involving this compound.
Used in Chemical Reactions:
Due to its complex structure and the presence of different atomic groups, 3-[(2-ethylhexyl)disulfanyl]methylheptane may be employed as a reactant in specific chemical processes, where its unique features could contribute to the formation of novel products or intermediates.

Check Digit Verification of cas no

The CAS Registry Mumber 79392-44-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,3,9 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 79392-44:
(7*7)+(6*9)+(5*3)+(4*9)+(3*2)+(2*4)+(1*4)=172
172 % 10 = 2
So 79392-44-2 is a valid CAS Registry Number.

79392-44-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[(2-ethylhexyldisulfanyl)methyl]heptane

1.2 Other means of identification

Product number -
Other names Disulfide, bis(2-ethylhexyl)

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:79392-44-2 SDS

79392-44-2Relevant articles and documents

VIC-IODOTHIOCYANATES AND IODOISOTHIOCYANATES. PART 6. THE SYNTHESIS OF THIIRANS

Cambie, Richard C.,Rutledge, Peter S.,Strange, Gary A.,Woodgate, Paul D.

, p. 1501 - 1510 (2007/10/02)

Treatment of the vic-iodothiocyanate of either cyclic or acyclic alkenes with lithium triethylborohydride ("Super Hydride") gives thiirans in high yields.The structure of the product from r-1-iodo-1-thiacyanatomethyl-c-4-t-butylcyclohexane has been confirmed by an independent synthesis.

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