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96-06-0

2,3-Epoxy-2,4,4-trimethyl pentane, also known as isopropylidene norcamphane, is a cyclic ether with the molecular formula C8H14O. It is a colorless liquid with a density of 0.84 g/cm3 and a boiling point of 130-132°C. 2,3-Epoxy-2,4,4-trimethyl pentane is derived from the reaction of 2,4,4-trimethyl-2-norbornanol with an oxidizing agent, such as peracetic acid or hydrogen peroxide, to form the epoxy ring. It is an important intermediate in the synthesis of various organic compounds, particularly in the production of pharmaceuticals and agrochemicals. Due to its reactive epoxy group and unique cyclic structure, 2,3-epoxy-2,4,4-trimethyl pentane has found applications in the preparation of various functionalized molecules and polymers.

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  • 96-06-0 Structure

  • Basic information

    1. Product Name: 2,3-Epoxy-2,4,4-trimethyl pentane
    2. Synonyms: 2,3-Epoxy-2,4,4-trimethyl pentane
    3. CAS NO:96-06-0
    4. Molecular Formula: C8H16O
    5. Molecular Weight: 128.21
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 96-06-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 119.5°Cat760mmHg
    3. Flash Point: 23.6°C
    4. Appearance: /
    5. Density: 0.86g/cm3
    6. Vapor Pressure: 19mmHg at 25°C
    7. Refractive Index: 1.428
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2,3-Epoxy-2,4,4-trimethyl pentane(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2,3-Epoxy-2,4,4-trimethyl pentane(96-06-0)
    12. EPA Substance Registry System: 2,3-Epoxy-2,4,4-trimethyl pentane(96-06-0)

  • 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: 96-06-0(Hazardous Substances Data)

96-06-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96-06-0 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 9 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 96-06:
(4*9)+(3*6)+(2*0)+(1*6)=60
60 % 10 = 0
So 96-06-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O/c1-7(2,3)6-8(4,5)9-6/h6H,1-5H3

96-06-0SDS

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 2,3-Epoxy-2,4,4-trimethylpentane

1.2 Other means of identification

Product number -
Other names Oxirane, 3-(1,1-dimethylethyl)-2,2-dimethyl-

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:96-06-0 SDS

96-06-0Relevant articles and documents

Aldehyde/Olefin Cooxidations: Parallel Epoxidation Pathways and Concerted Decomposition of the Peroxyacyl-Olefin Adduct

Lassila, Kevin R.,Waller, Francis J.,Werkheiser, Steven E.,Wressell, Amy L.

, p. 8077 - 8080 (2007/10/02)

Aldehyde-mediated olefin epoxidations appear to proceed by parallel peracid and radical addition pathways.For that portion of the reaction proceeding by radical addition, several lines of evidence favor an explanation in which the peroxyacyl-olefin adduct decomposes in a concerted manner to form alkyl radical, CO2, and epoxide.

Studies on the Autoxidation of Branched-chain Olefins. I. Autoxidation of 2-Methylalk-1-enes and 2-Methylalk-2-enes

Bilas, W.,Hoebold, W.,Pritzkow, W.

, p. 125 - 141 (2007/10/02)

The products of the autoxidation of 2-methylpent-1-ene, 2-methylpent-2-ene, 2-methylhex-1-ene, 2-methylhex-2-ene, 2,4,4-trimethylpent-1-ene, and 2,4,4-trimethylpent-2-ene were analyzed by gas chromatography.The identification of the products corresponding to the individual peaks was possible by comparison with authentic substances or by preparative gaschromatographic separation and n.m.r.-spectroscopy of the isolated samples.In this way not only the epoxides and the products of the oxidative cleavage of the C=C double bond but also the allylic alcohols formed by LiAlH4-reduction of the oxidation mixtures could be identified and analyzed.From the results the compositions of the original oxidation mixtures were calculated.

Untersuchungen zur Kinetik und zum Mechanismus der Isooctanoxydation

Lischke, G.,Oehlmann, G.

, p. 555 - 572 (2007/10/02)

Isooctan wurde mit Sauerstoff in einem statischen Reaktor aus Rasothermglas im Temperaturbereich zwischen 538 K und 593 K oxydiert.Aus kinetischen Untersuchungen folgt fuer den Bereich der stationaeren Reaktionsgeschwindigkeit ein Zeitgesetz rstat = k32.Die scheinbare Aktivierungsenergie betraegt: EA = 220 +/- 3 kJ/mol.Als charakteristische Reaktionsprodukte wurden 2,2,4,4-Tetramethyltetrahydrofuran, 2-tert.-Butyl-3-methyl-oxetan, α-Diisobuten, β-Diisobuten, β-Diisobutenoxid, Isooktanon sowie 2,2-Dimethylpentanon-3 und -4 gefunden.Aus der Verschiedenartigkeit der Produkte der Isooctanoxydation zu denen der Diisobutenoxydation folgt, dass bei der Alkanoxydation das strukturanaloge Olefin parallel mit anderen sauerstoffhaltigen Produkten gebildet wird.Isootylhydroperoxide koennen unter den Reaktionsprodukten nicht nachgewiesen werden.Durch das Fehlen C-zahlgleicher Hydroperoxide unterscheidet sich iso-Octan hinsichtlich seines Oxydationsverhaltens in charakteristischer Weise von unverzweigten Kohlenwasserstoffen (z.B. n-Heptan).Ein Reactionsmechanismus wird vorgeschlagen.

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