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144424-48-6

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144424-48-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144424-48-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,4,2 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 144424-48:
(8*1)+(7*4)+(6*4)+(5*4)+(4*2)+(3*4)+(2*4)+(1*8)=116
116 % 10 = 6
So 144424-48-6 is a valid CAS Registry Number.

144424-48-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-di-t-butyl-3-(2,4,6-tri-t-butylphenyl)thiirane

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:144424-48-6 SDS

144424-48-6Relevant articles and documents

Reactions of (2,4,6-Tri-t-butyl)thiobenzaldehyde with Diazo Compounds. Synthesis and Reactions of Sterically Congested Thiiranes

Watanabe, Soichiro,Kawashima, Takayuki,Tokitoh, Norihiro,Okazaki, Renji

, p. 1437 - 1448 (2007/10/02)

Sterically congested thiiranes having a 2,4,6-tri-t-butylphenyl group were synthesized by the reactions of (2,4,6-tri-t-butyl)thiobenzaldehyde with sterically hindered diazo compounds.Thermal desulfurization of the most congested thiirane, 2,2-di-t-butyl-3-(2,4,6-tri-t-butylphenyl)thiirane (15c), did not proceed even upon using highly reactive reagents, such as hexamethylphosphorous triamide or organolithiums.The photoreaction of 15c did not give the corresponding styrene, but afforded several products containing 2,4,6-tri-t-butylbenzothiophene and Dewar benzenes,2,2-di-t-butyl-3-(3,4,6-tri-t-butylbicyclohexa-2,5-dien-2-yl)thiirane and 2-t-butyl-3,3-dimethyl-1-(1,3,5-tri-t-butylbicyclohexa-2,5-diene-2-yl)-1-butene (24), the latter of which is the first example for a vinyl-substituted Dewar benzene.Compound 24 has a unique reactivity, giving a rearrangement product, 2-t-butyl-3,3-dimethyl-1-(1,3,5-tri-t-butylbicyclohexa-2,5-diene-2-yl)-1-butene on thermolysis.

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