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CAS

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2167-38-6

3-Methyloxetane is a chemical compound that belongs to the organic chemical class named oxetanes. It is characterized by an oxetane (or 1,3-propanediol) ring, which consists of three carbon atoms and one oxygen atom. The unique molecular structure of 3-methyloxetane features a methyl group attached, endowing it with specific properties that set it apart from other oxetanes. 3-methyloxetane is utilized in a variety of industrial and scientific applications, but it is important to handle it with caution due to potential safety hazards.

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  • 2167-38-6 Structure

  • Basic information

    1. Product Name: 3-methyloxetane
    2. Synonyms: 3-methyloxetane;Oxetane, 3-Methyl-
    3. CAS NO:2167-38-6
    4. Molecular Formula: C4H8O
    5. Molecular Weight: 72.1057
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 2167-38-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 59 °C at 760 mmHg
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 0.879 g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-methyloxetane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-methyloxetane(2167-38-6)
    11. EPA Substance Registry System: 3-methyloxetane(2167-38-6)

  • 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: 2167-38-6(Hazardous Substances Data)

2167-38-6 Usage

Uses

Used in Chemical Synthesis:
3-Methyloxetane is used as a building block in the synthesis of various organic compounds. Its unique structure allows for the creation of a wide range of molecules with different functional groups, making it a valuable intermediate in the chemical industry.
Used in Pharmaceutical Research:
3-Methyloxetane is employed as a starting material in the development of new pharmaceutical compounds. Its versatile structure can be modified to create potential drug candidates, contributing to the advancement of medicine and healthcare.
Used in Material Science:
3-Methyloxetane is used as a component in the formulation of new materials with specific properties. Its incorporation into polymers and other materials can lead to the development of innovative products with improved characteristics, such as enhanced strength, flexibility, or chemical resistance.
Used in Analytical Chemistry:
3-Methyloxetane is utilized as a reference compound or internal standard in analytical chemistry. Its distinct properties can be used to calibrate instruments and ensure accurate measurements in various analytical techniques, such as chromatography and spectroscopy.
Used in Research and Development:
3-Methyloxetane is employed as a research tool in various scientific fields. Its unique structure and reactivity make it an interesting subject for studies on chemical reactions, mechanisms, and the development of new synthetic methods.

Check Digit Verification of cas no

The CAS Registry Mumber 2167-38-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,6 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2167-38:
(6*2)+(5*1)+(4*6)+(3*7)+(2*3)+(1*8)=76
76 % 10 = 6
So 2167-38-6 is a valid CAS Registry Number.

2167-38-6SDS

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-methyloxetane

1.2 Other means of identification

Product number -
Other names 3-methyl-oxetane

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:2167-38-6 SDS

2167-38-6Relevant articles and documents

OXYGEN YLIDES-I. REACTIONS OF CARBENES WITH OXETANE

Friedrich, Klaus,Jansen, Ulrich,Kirmse, Wolfgang

, p. 193 - 196 (2007/10/02)

The ylides generated from carbenes (:CH2, :CHCO2Et, :CHPh) and oxetane in the presence of methanol undergo Stevens rearrangement and protonation competitively, yielding tetrahydrofurans and 1,3-dialkoxycyclopropanes as major products.

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