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(n-pentyl)diphenylphosphane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77423-29-1

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77423-29-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77423-29-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,4,2 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 77423-29:
(7*7)+(6*7)+(5*4)+(4*2)+(3*3)+(2*2)+(1*9)=141
141 % 10 = 1
So 77423-29-1 is a valid CAS Registry Number.

77423-29-1SDS

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 (n-pentyl)diphenylphosphane

1.2 Other means of identification

Product number -
Other names diphenylpentylphosphine

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:77423-29-1 SDS

77423-29-1Relevant academic research and scientific papers

Palladium-catalyzed C(sp3)–P(III) bond formation reaction with acylphosphines as phosphorus source

Zhang, Mengyue,Ma, Zhichao,Du, Hongguang,Wang, Zhiqian

, (2020/06/29)

Palladium-catalyzed C(sp3)–P(III) bond formation reaction for alkyl substituted phosphines preparation was developed. In this reaction, various alkyl bromides and limited alkyl chlorides reacted with acylphosphine under relative mild and easily accessible condition, and differential phosphines were afforded in good yields. This reaction made up the application of palladium catalysis in C(sp3)–P(III) bond formation, and indicated a practical application of acylphosphine as a phosphination reagent.

Homolytic substitution at phosphorus for the synthesis of alkyl and aryl phosphanes

Vaillard, Santiago E.,Mueck-Lichtenfeld, Christian,Grimme, Stefan,Studer, Armido

, p. 6533 - 6536 (2008/09/17)

(Chemical Equation Presented) A transition-metal-free radical phosphonation using Me3SnPPh2 and the less toxic Me 3SiPPh2 is reported. These readily available reagents react highly efficiently with primary and secondary alkyl radicals. Moreover, aryl radicals and tertiary alkyl radicals are phosphonated with Me 3SnPPh2 (see scheme; R = aryl, alkyl, vinyl; X = 1, Br, OC(S)imidazolyl). DFT calculations provide insights into the mechanism of the reaction.

Alane - A novel way to reduce phosphine oxides

Griffin, Sara,Heath, Lucy,Wyatt, Paul

, p. 4405 - 4406 (2007/10/03)

Phosphine oxides may be reduced to phosphines in excellent yield using alane - AIH3. An aqueous workup is not required.

The Stereochemistry of Organometallic Compounds. XXXVII. Regio- and Stereo-control in the Rhodium-Catalysed Hydroformylation of Some Alkenylphosphines

Jackson, W. Roy,Perlmutter, Patrick,Suh, Guem-Hee,Tasdelen, E. Elizabeth

, p. 951 - 966 (2007/10/02)

Good to excellent regiocontrol can be obtained for the internal product of rhodium-catalysed hydroformylation of a range of alkenylphosphines.Excellent stereo- as well as regio-control can also be obtained for reactions of some cyclic alkenylphosphines.

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