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29949-84-6

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29949-84-6 Usage

Chemical Properties

White to almost white crystalline powder

Uses

suzuki reaction

Check Digit Verification of cas no

The CAS Registry Mumber 29949-84-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,9,4 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 29949-84:
(7*2)+(6*9)+(5*9)+(4*4)+(3*9)+(2*8)+(1*4)=176
176 % 10 = 6
So 29949-84-6 is a valid CAS Registry Number.
InChI:InChI=1/C21H21O3P/c1-22-16-7-4-10-19(13-16)25(20-11-5-8-17(14-20)23-2)21-12-6-9-18(15-21)24-3/h4-15H,1-3H3

29949-84-6 Well-known Company Product Price

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  • Alfa Aesar

  • (A17949)  Tris(3-methoxyphenyl)phosphine, 98%   

  • 29949-84-6

  • 1g

  • 713.0CNY

  • Detail
  • Alfa Aesar

  • (A17949)  Tris(3-methoxyphenyl)phosphine, 98%   

  • 29949-84-6

  • 5g

  • 2896.0CNY

  • Detail

29949-84-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name tris(3-methoxyphenyl)phosphane

1.2 Other means of identification

Product number -
Other names Tris(m-anisyl)phosphine

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:29949-84-6 SDS

29949-84-6Relevant articles and documents

Photocatalytic Arylation of P4 and PH3: Reaction Development Through Mechanistic Insight

Cammarata, Jose,Gschwind, Ruth M.,Lennert, Ulrich,Rothfelder, Robin,Scott, Daniel J.,Streitferdt, Verena,Wolf, Robert,Zeitler, Kirsten

supporting information, p. 24650 - 24658 (2021/10/14)

Detailed 31P{1H} NMR spectroscopic investigations provide deeper insight into the complex, multi-step mechanisms involved in the recently reported photocatalytic arylation of white phosphorus (P4). Specifically, these studies have identified a number of previously unrecognized side products, which arise from an unexpected non-innocent behavior of the commonly employed terminal reductant Et3N. The different rate of formation of these products explains discrepancies in the performance of the two most effective catalysts, [Ir(dtbbpy)(ppy)2][PF6] (dtbbpy=4,4′-di-tert-butyl-2,2′-bipyridine) and 3DPAFIPN. Inspired by the observation of PH3 as a minor intermediate, we have developed the first catalytic procedure for the arylation of this key industrial compound. Similar to P4 arylation, this method affords valuable triarylphosphines or tetraarylphosphonium salts depending on the steric profile of the aryl substituents.

Organocatalyzed Reduction of Tertiary Phosphine Oxides

Schirmer, Marie-Luis,Jopp, Stefan,Holz, Jens,Spannenberg, Anke,Werner, Thomas

supporting information, p. 26 - 29 (2016/01/25)

A novel selective catalytic reduction method of tertiary phosphine oxides to the corresponding phosphines has been developed. Notably, the reaction proceeds smoothly with low catalyst loadings of 1-5 mol% even at low temperature (70 C). Under the optimized conditions various phosphine oxides could be selectively reduced and the desired phosphines were usually obtained in excellent yields above 90%. Furthermore, we have developed a one-pot reaction sequence for the preparation of valuable phosphinborane adducts. Simple addition of BH3THF subsequent to the reduction step gave the desired adducts in yields up to 99%.

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