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55395-25-0

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55395-25-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55395-25-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,3,9 and 5 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 55395-25:
(7*5)+(6*5)+(5*3)+(4*9)+(3*5)+(2*2)+(1*5)=140
140 % 10 = 0
So 55395-25-0 is a valid CAS Registry Number.

55395-25-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethylidene(dimethyl)silane

1.2 Other means of identification

Product number -
Other names 1,1,2-trimethylsilene

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:55395-25-0 SDS

55395-25-0Downstream Products

55395-25-0Relevant articles and documents

Matrix Isolation of Silenes and Their Ultraviolet Absorptions

Sekiguchi, Akira,Ando, Wataru

, p. 2025 - 2026 (1986)

Various silenes were isolated in 3-methylpentane matrix at 77 K by photolysis of the corresponding silyl diazo compounds and their ultraviolet spectra were measured.

Oxidation of methylsilenes with molecular oxygen. A matrix isolation study

Trommer, Martin,Sander, Wolfram,Patyk, Andreas

, p. 11775 - 11783 (2007/10/02)

The photochemical and thermal oxidation of 1-methylsilene (2-silapropene) (1a), 1,1-dimethylsilene (1b), and 1,1,2-trimethylsilene (1c) has been investigated in O2-doped argon matrices. All silenes 1 are easily photooxidized in matrices containing more than 1% O2, but trimethylsilene (1c) is the only silene that exhibits thermal reactivity toward oxygen at temperatures as low as 20-40 K. The photochemical reactivity increases from 1a to 1c with increasing number of methyl groups at the double bond and decreasing ionization potential. Key intermediates in both the photochemical and the thermal oxidation of 1 are siladioxetanes 9. These species are labile even in low-temperature matrices and could not be identified spectroscopically, but evidence comes from the observed oxidation products such as a complex between methylsilanone and formaldehyde 8a and the formylsilanols 10. An additional oxidation pathway is observed for 1c with a methyl group at the C-atom of the silene moiety. Here, the primary adduct of 1c and 3O2, triplet-diradical T-21c, can either ring-close to give dioxetane 9c and the products derived of it or produce dimethylvinylsilyl hydroperoxide (22) via H-abstraction from a methyl group.

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