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2,2,3,3,5,5,6,6-Octamethyl-1,4-diaza-2,3,5,6-tetrasilacyclohexane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15164-14-4

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15164-14-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15164-14-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,1,6 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 15164-14:
(7*1)+(6*5)+(5*1)+(4*6)+(3*4)+(2*1)+(1*4)=84
84 % 10 = 4
So 15164-14-4 is a valid CAS Registry Number.

15164-14-4SDS

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 2,2,3,3,5,5,6,6-octamethyl-1,4,2,3,5,6-diazatetrasilinane

1.2 Other means of identification

Product number -
Other names 2,2,3,3,5,5,6,6-Octamethyl-1,4-diaza-2,3,5,6-tetrasilacyclohexane

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:15164-14-4 SDS

15164-14-4Downstream Products

15164-14-4Relevant academic research and scientific papers

Novel Inorganic Ringsystems. 36. A Novel Ninemembered Cyclosilazane System and New Compounds in the Class of Cyclotetrasiladiazanes

Wannagat, Ulrich,Blumenthal, Tomas

, p. 557 - 568 (1985)

The formerly unknown Si-dodecamethyl-cyclo-hexasila-3,6,9-triazane (-Sime2Sime2NH-)3 (4) was detected in low yield (3-5percent) among the reaction products of dichlortetramethyldisilane and ammonia.The already known main product (50percent) Si-octamethyl-cyclo-tetrasila-3,6-diazane (-Sime2Sime2NH-)2 (3) reacted after metallation with chloromethylsilanes menSiCl4-n (n = 0 - 3) to give the N,N'-disubstituted cyclotetrasiladiazanes 11-14, from which 12 was transformed with ammonia to the corresponding N,N'-bis(aminodimethylsilyl) derivative 15, and 13 with metallated methylamine to the corresponding N,N'-bisderivative 16.Attempts to construct novel SiN frameworks (g) or (k)-(m) failed. - Keywords: Silicon-nitrogen compounds; Cyclohexasilatriazane; Cyclotetrasiladiazane derivatives

Coordination polymers of alkali metal cyclosiloxazanides with one- and two-dimensional structures

Balmer, Markus,Dankert, Fabian,Jost, Maximilian,Peters, Bertram,Richter, Roman-Malte,von H?nisch, Carsten

, p. 5787 - 5790 (2020)

The reaction of O(Si2Me4Cl)2with ammonia yielded the cyclic siloxazane O(Si2Me4)2NH (1), which was used as a precursor for the synthesis of siloxazanide-type alkali metal salts. The metalation of1with the strong bases BzA (A = Na, K, Rb, Cs and Bz = benzyl) results in different dimensional structures depending on the alkali metal ion used. These results give new insights into framework design with inorganic building blocks and the coordination ability of siloxanes.

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