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2167-38-6

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2167-38-6 Usage

General Description

3-Methyloxetane is a chemical compound classified under the organic chemical class named oxetanes. Oxetanes make part of organic compounds containing an oxetane (or 1,3-propanediol) ring with three carbon atoms and one oxygen atom. The particular molecular structure of 3-methyloxetane includes a methyl group attached, giving it the specific properties that distinguish it from other oxetanes. This chemical is used in various industrial and scientific applications. However, like many other chemicals, it is advisable to handle it with care as it may pose some safety hazards.

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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