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2-ETHYLUNDECANOIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 45158-84-7 Structure
  • Basic information

    1. Product Name: 2-ETHYLUNDECANOIC ACID
    2. Synonyms: 2-ETHYLUNDECANOIC ACID
    3. CAS NO:45158-84-7
    4. Molecular Formula: C13H26O2
    5. Molecular Weight: 214.34
    6. EINECS: 256-197-0
    7. Product Categories: N/A
    8. Mol File: 45158-84-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 307.44°C (estimate)
    3. Flash Point: 176.7°C
    4. Appearance: /
    5. Density: 0.8466 (rough estimate)
    6. Vapor Pressure: 5.4E-05mmHg at 25°C
    7. Refractive Index: 1.4274 (estimate)
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 4.82±0.25(Predicted)
    11. CAS DataBase Reference: 2-ETHYLUNDECANOIC ACID(CAS DataBase Reference)
    12. NIST Chemistry Reference: 2-ETHYLUNDECANOIC ACID(45158-84-7)
    13. EPA Substance Registry System: 2-ETHYLUNDECANOIC ACID(45158-84-7)
  • 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: 45158-84-7(Hazardous Substances Data)

45158-84-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 45158-84-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,5,1,5 and 8 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 45158-84:
(7*4)+(6*5)+(5*1)+(4*5)+(3*8)+(2*8)+(1*4)=127
127 % 10 = 7
So 45158-84-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H26O2/c1-3-5-6-7-8-9-10-11-12(4-2)13(14)15/h12H,3-11H2,1-2H3,(H,14,15)

45158-84-7SDS

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 2-ETHYLUNDECANOIC ACID

1.2 Other means of identification

Product number -
Other names 2-Aethyl-undecylsaeure

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:45158-84-7 SDS

45158-84-7Relevant articles and documents

Ruthenium-catalysed hydroxycarbonylation of olefins

Dühren, Ricarda,Kucmierczyk, Peter,Jackstell, Ralf,Franke, Robert,Beller, Matthias

, p. 2026 - 2030 (2021/04/09)

State-of-the-art catalyst systems for hydroxy- and alkoxycarbonylations of olefins make use of palladium complexes. In this work, we report a complementary ruthenium-catalysed hydroxycarbonylation of olefins applying an inexpensive Ru-precursor (Ru3(CO)12) and PCy3as a ligand. Crucial for the success of this transformation is the use of hexafluoroisopropanol (HFIP) as the solvent in the presence of an acid co-catalyst (PTSA). Overall, moderate to good yields are obtained using aliphatic olefins including the industrially relevant substrate di-isobutene. This atom-efficient catalytic transformation provides straightforward access to various carboxylic acids from unfunctionalized olefins.

Manufacture of C13 higher fatty acids from their esters by carbonylation of dodecene-1 in ionic liquid medium

Lapidus,Eliseev,Bondarenko,Chau

experimental part, p. 442 - 449 (2011/10/03)

The effect of catalyst nature, temperature, acidity, promoters, and feedstock composition on dodecene-1 carbonylation in the presence of Pd compounds in an ionic liquid medium yielding higher fatty acid and their esters was studied. Palladium salts without phosphine ligands show high activity in tetrabutylammonium bromide. In systems of this kind, the catalyst is suspended in the reaction mass in the form of Pd particles with a size of 4-10 nm. It was shown that the catalytic system can be repeatedly used without loss of activity. It is acceptable to use synthesis gas instead of bare carbon monoxide with the selectivity for tride-canoic acid increasing.

3-Nonyltetrahydrofuran from the Reduction of Alkenes with Lithium and Ethanol in Ammonia

Massy-Westropp, Ralph A.,Warren, Richard F. O.

, p. 1969 - 1977 (2007/10/02)

3-Nonylidenetetrahydrofuran is readily reduced with lithium and ethanol in ammonia to yield mainly 3-nonyltetrahydrofuran together with 3-methyldodecan-1-ol.The reductions of a mixture of 4-nonyl-4,5-dihydrofuran and 3-nonyl-2,5-dihydrofuran and of a mixture of 3-nonyl-4,5-dihydrofuran, 3-nonyl-2,5-dihydrofuran and 3-nonylidenetetrahydrofuran are also reported.

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