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Phosphine, [2,2-dimethyl-1-[(trimethylsilyl)oxy]propylidene]phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60820-29-3

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60820-29-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60820-29-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,8,2 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 60820-29:
(7*6)+(6*0)+(5*8)+(4*2)+(3*0)+(2*2)+(1*9)=103
103 % 10 = 3
So 60820-29-3 is a valid CAS Registry Number.

60820-29-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,2-dimethyl-1-trimethylsilyloxypropylidene)-phenylphosphane

1.2 Other means of identification

Product number -
Other names Phosphine,[2,2-dimethyl-1-[(trimethylsilyl)oxy]propylidene]phenyl

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:60820-29-3 SDS

60820-29-3Relevant academic research and scientific papers

Low Coordinated Phosphorus Compounds, 17. Diphosphabutadienes

Appel, Rolf,Barth, Volker,Knoch, Falk

, p. 938 - 950 (2007/10/02)

The reaction of the silylated phosphaalkene 1 with hexachloroethane (2) yields the chlorophosphaalkene 3, which reacts with additional 1 under chlorotrimethylsilane elimination to give the first 2,3-diphosphabutadiene 6.This can be prepared as well from the persilylated diphosphane 4 and 2,2-dimethylpropionyl chloride (5).The spectroscopic and x-ray data of 6 are discussed.Experiments for the preparation of the 1,4-diphosphabutadienes 11a, b from the organylbis(trimethylsilyl)phosphanes 9a, b and oxalyl chloride yield the correspondingly substituted 3,4-diphosphacyclo butenes 12a, b.The reaction of 1 with phosgene and isocyanide dichloride 14b yields instead of the expected 1,3-diphosphabutadienes 16a, b the 1,3-diphosphacyclobutenes 17a, b, whose structure is affirmed by x-ray structure determination of 7a.The formation of the cyclobutenes 12a, b and 17a, b is discussed.

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