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24300-21-8

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24300-21-8 Usage

Uses

Propionitrile-3,3,3-d3 (CAS# 24300-21-8) is a useful isotopically labeled research compound.

Check Digit Verification of cas no

The CAS Registry Mumber 24300-21-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,0 and 0 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 24300-21:
(7*2)+(6*4)+(5*3)+(4*0)+(3*0)+(2*2)+(1*1)=58
58 % 10 = 8
So 24300-21-8 is a valid CAS Registry Number.

24300-21-8SDS

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 PROPIONITRILE-3,3,3-D3

1.2 Other means of identification

Product number -
Other names 3,3,3-trideuterio-propionitrile

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:24300-21-8 SDS

24300-21-8Downstream Products

24300-21-8Relevant articles and documents

The effect of solvent on the structure of the transition state for the SN2 reaction between cyanide ion and ethyl chloride in DMSO and THF probed with six different kinetic isotope effects

Fang, Yao-Ren,MacMillar, Susanna,Eriksson, Jonas,Kolodziejska-Huben, Magdalena,Dybala-Defratyka, Agnieszka,Paneth, Piotr,Matsson, Olle,Westaway, Kenneth Charles

, p. 4742 - 4747 (2007/10/03)

The secondary α- and β-deuterium, the α-carbon, the nucleophile carbon, the nucleophile nitrogen, and the chlorine leaving group kinetic isotope effects for the SN2 reaction between cyanide ion and ethyl chloride were determined in the very slightly polar solvent THF at 30 °C. A comparison of these KIEs with those reported earlier for the same reaction in the polar solvent DMSO shows that the transition state in THF is only slightly tighter with very slightly shorter NC-Cα and Cα-Cl bonds. This minor change in transition state structure does not account for the different transition structures that were earlier suggested by interpreting the experimental KIEs and the gas-phase calculations, respectively. It therefore seems unlikely that the different transition states suggested by the two methods are due to the lack of appropriate solvent modeling in the theoretical calculations. Previously it was predicted that the transition state of SN2 reactions where the nucleophile and the leaving group have the same charge would be unaffected by a change in solvent. The experimental KIEs support this view.

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