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1,2-PROPYLENE-3,3,3-D3 OXIDE, also known as (±)-1,2-Propylene-3,3,3-d3 Oxide (CAS# 2245-32-1), is an isotopically labeled research compound that is valuable for various scientific investigations and experiments.

2245-32-1

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2245-32-1 Usage

Uses

Used in Research Applications:
1,2-PROPYLENE-3,3,3-D3 OXIDE is used as a research compound for its isotopically labeled properties, which allow for enhanced tracking and analysis in various scientific studies and experiments. 1,2-PROPYLENE-3,3,3-D3 OXIDE is particularly useful in fields that require precise measurements and observations, such as chemistry, biochemistry, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 2245-32-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,4 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2245-32:
(6*2)+(5*2)+(4*4)+(3*5)+(2*3)+(1*2)=61
61 % 10 = 1
So 2245-32-1 is a valid CAS Registry Number.

2245-32-1SDS

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 1,2-PROPYLENE-3,3,3-D3 OXIDE

1.2 Other means of identification

Product number -
Other names trideuteriomethyl

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:2245-32-1 SDS

2245-32-1Upstream product

2245-32-1Downstream Products

2245-32-1Relevant academic research and scientific papers

REARRANGEMENT AND METHYL LOSS FROM IONIZED PROPENE OXIDE AND METHYL VINYL ETHER.

Turecek,McLafferty

, p. 2528 - 2531 (1984)

Molecular cations of propene oxide (a) and methyl vinyl ether (b), despite a large difference (35 kcal mol** minus **1) in their heats of formation, undergo two very similar metastable methyl loss dissociations; for both of these dissociations a and b exhibit the same kinetic energy release values and produce acetyl ions. Deuterium labeling shows that a ions undergo little direct methyl loss, but instead isomerize by ring opening and 1,4-H transfer to b. For long-lived ions of energies below the decomposition threshold, nearly complete hydrogen exchange occurs between the methyl and methylene groups.

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