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1,3-Disilacyclobutane is a cyclic compound consisting of two silicon atoms and four carbon atoms, with the molecular formula C4H12Si2. It features a four-membered ring structure, where the silicon atoms are bonded to each other and to two carbon atoms, while the remaining carbon atoms are bonded to hydrogen. 1,3-Disilacyclobutane is a derivative of cyclobutane, with silicon replacing two of the carbon atoms. 1,3-Disilacyclobutane is of interest in organosilicon chemistry due to its unique structure and potential applications in materials science and as a precursor in the synthesis of more complex organosilicon compounds.

287-55-8

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287-55-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 287-55-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,8 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 287-55:
(5*2)+(4*8)+(3*7)+(2*5)+(1*5)=78
78 % 10 = 8
So 287-55-8 is a valid CAS Registry Number.

287-55-8SDS

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 1,3-disiletane

1.2 Other means of identification

Product number -
Other names 1,3-Disilacylcyclobutan

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:287-55-8 SDS

287-55-8Relevant academic research and scientific papers

Hetero-?-Systems, 8. Silaethene

Maier, Guenther,Mihm, Gerhard,Reisenauer, Hans Peter

, p. 2351 - 2368 (2007/10/02)

By means of a combination of vacuum flash pyrolysis and matrix isolation silaethene (1a) and its simply substituted derivatives 1b-f can be prepared starting with precursors 9a-f of the silabicyclooctadiene type.Silaolefins 1a-f are stable in argon at 10 K and can be identified by their characteristic IR and UV spectra.

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