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[(2,5-dimethylbenzene-1,4-diyl)dimethanediyl]bis(trimethylsilane) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69020-19-5

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69020-19-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69020-19-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,0,2 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 69020-19:
(7*6)+(6*9)+(5*0)+(4*2)+(3*0)+(2*1)+(1*9)=115
115 % 10 = 5
So 69020-19-5 is a valid CAS Registry Number.

69020-19-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name [2,5-dimethyl-4-(trimethylsilylmethyl)phenyl]methyl-trimethylsilane

1.2 Other means of identification

Product number -
Other names 1,4-bis(trimethylsilylmethyl)-3,6-dimethyl-benzen

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:69020-19-5 SDS

69020-19-5Downstream Products

69020-19-5Relevant academic research and scientific papers

Palladium-catalyzed C(sp 3)-C(sp 2) cross-coupling of (trimethylsilyl)methyllithium with (hetero)aryl halides

Heijnen, Dorus,Hornillos, Valentín,Corbet, Brian P.,Giannerini, Massimo,Feringa, Ben L.

, p. 2262 - 2265 (2015)

The palladium-catalyzed direct cross-coupling of a range of organic chlorides and bromides with the bifunctional C(sp3)-(trimethylsilyl)methyllithium reagent is reported. The use of Pd-PEPPSI-IPent as the catalyst allows for the preparation of structurally diverse and synthetically versatile benzyl- and allylsilanes in high yields under mild conditions (room temperature) with short reaction times.

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