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Phosphorane, cyclopentylidenetriphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21482-00-8

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21482-00-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21482-00-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,4,8 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 21482-00:
(7*2)+(6*1)+(5*4)+(4*8)+(3*2)+(2*0)+(1*0)=78
78 % 10 = 8
So 21482-00-8 is a valid CAS Registry Number.

21482-00-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclopentylidenetriphenylphosphorane

1.2 Other means of identification

Product number -
Other names -

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:21482-00-8 SDS

21482-00-8Relevant academic research and scientific papers

Silver-Catalysed Hydroarylation of Highly Substituted Styrenes

Dalton, Toryn,Gre?ies, Steffen,Das, Mowpriya,Niehues, Maximilian,Schrader, Malte L.,Gutheil, Christian,Ravoo, Bart Jan,Glorius, Frank

supporting information, p. 8537 - 8541 (2021/03/16)

Hydroarylation is an effective strategy to rapidly increase the complexity of organic structures by transforming flat alkene moieties into three-dimensional frameworks. Many strategies have already been developed to achieve the hydroarylation of styrenes,

A convenient synthesis of perfluoroalkylated allylic sulfides

Shen, Yanchang,Liao, Qimu

, p. 251 - 254 (2007/10/02)

Perfluoroalkylated allylic sulfides can be synthesized by the reaction of thiophenoxymethyl lithium with fluorinated β-oxoalkylphosphonium salts in 51percent-72percent yields. - Keywords: Synthesis; Perfluoroalkylated allylic sulfides; NMR spectroscopy; I

Novel Synthesis of Conjugated Bisperfluoroalkyl Enynes

Shen, Yanchang,Xiang, Yuejun,Qiu, Weiming

, p. 2965 - 2968 (2007/10/02)

Conjugated bisperfluoroalkyl enynes can be conveniently synthesized in 85-99percent yield by vacuum pyrolysis of (perfluoroacyl)methylene>triphenylphosphoranes which were generated from the corresponding methylene triphenylphosphoranes via double perfluoroacylation in a one-pot reaction.

Novel One-Pot Synthesis of 4-Trifluoromethyl-2,4-dienamides

Shen, Yanchang,Xiang, Yuejun

, p. 2493 - 2494 (2007/10/02)

4-Trifluoromethyl-2,4-dienamides can be successfully synthesized by the reaction of trifluoromethylated arsoranes, generated from the transylidation between fluorinated β-oxoalkylphosphonium salts and methylenetriphenylarsorane, with α-bromoacetamides.

A novel generation of perfluoroalkylated enolates by reductive cleavage of fluorinated β-ketophosphonium salts

Shen, Yanchang,Xiang, Yuejun,Qiu, Weiming

, p. 4953 - 4954 (2007/10/02)

A novel generation of perfluoroalkylated enolates by reductive cleavage of fluorinated β-ketophosphonium salts and its application to the synthesis of perfluoroalkylated vinyl esters, β-hydroxy ketones, vinyl ether and ketone are described.

A novel double elimination of arsonium salts. One-pot synthesis of 4-trifluoromethyl-2,4-dienyl carboxylates

Shen,Xiang

, p. 2305 - 2306 (2007/10/02)

A novel double elimination of arsonium salts and its application to the synthesis of 4-trifluoromethyl-2,4-dienyl carboxylates are described.

A Novel Synthesis of α-Fluoroalkylvinyl- or α-Fluoroepoxyalkyl-phosphonate

Shen, Yanchang,Liao, Qimu,Qiu, Weiming

, p. 695 - 697 (2007/10/02)

α-Fluoroalkylvinyl- or α-fluoroepoxyalkyl-phosphonates can be synthesized by the reaction of diethyl lithium phosphite with fluorinated β-oxoalkylphosphonium salts, depending upon the α-substituents R1 and R2 in the alkylidene moiety of the phosphorane us

A Novel One-pot Synthesis of Fluoroenynes

Shen, Yanchang,Qui, Weiming

, p. 703 - 704 (2007/10/02)

A novel one-pot synthesis of fluoroenynes via eliminative nucleophilic addition of β-ketophosphonium salts to acetylide anions is described.

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