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Silane, (6-bromo-2-hexynyl)trimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112129-48-3

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112129-48-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112129-48-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,1,2 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 112129-48:
(8*1)+(7*1)+(6*2)+(5*1)+(4*2)+(3*9)+(2*4)+(1*8)=83
83 % 10 = 3
So 112129-48-3 is a valid CAS Registry Number.

112129-48-3SDS

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 6-bromohex-2-ynyl(trimethyl)silane

1.2 Other means of identification

Product number -
Other names (6-bromohex-2-ynyl)trimethylsilane

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:112129-48-3 SDS

112129-48-3Relevant academic research and scientific papers

Cyclobutene formation accompanying an intramolecular Lewis acid-promoted spirocyclization of a propargylic silane

Spence, John D.,Lowrie, Lee E.,Nantz, Michael H.

, p. 5499 - 5502 (1995)

An intramolecular Lewis acid-promoted conjugate addition of a propargylic silane to a functionalized cyclohex-2-en-1-one resulted in part in the remarkable formation of a highly fused cyclobutene. The reaction was found to be dependent on the stoichiometr

AN N-ACYLIMINIUM ROUTE TO THE 8-AZABICYCLOOCTANE (TROPANE) AND THE 9-AZABICYCLONONANE RIG SYSTEM SYNTHESIS OF (+/-)-ANATOXIN-A

Esch, Peter M.,Hiemstra, Henk,Klaver, Wim J.,Speckamp, W. Nico

, p. 75 - 79 (2007/10/02)

Propargyl and allyl silanes 20-22, readily prepared from succinimide, cyclize on dissolution in formic acid to azabicycles 23-25 in excellent yields.

INTRAMOLECULAR CYCLIZATIONS OF ALLYL- AND PROPARGYLSILANES

Schinzer, Dieter,Solyom, Sandor,Becker, Marion

, p. 1831 - 1834 (2007/10/02)

Allylsilanes of type 5 and propargylsilanes of type 13 undergo efficient cyclizations upon treatment with EtAlCl2 in toluene to afford stereoselectively functionalized hydrindanones of type 6 and spirodecanes of type 14.

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