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896-33-3

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896-33-3 Usage

Chemical Properties

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Check Digit Verification of cas no

The CAS Registry Mumber 896-33-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,9 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 896-33:
(5*8)+(4*9)+(3*6)+(2*3)+(1*3)=103
103 % 10 = 3
So 896-33-3 is a valid CAS Registry Number.
InChI:InChI=1/C20H20P.ClH/c1-2-21(18-12-6-3-7-13-18,19-14-8-4-9-15-19)20-16-10-5-11-17-20;/h3-17H,2H2,1H3;1H/q+1;/p-1

896-33-3 Well-known Company Product Price

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  • Alfa Aesar

  • (B23015)  Ethyltriphenylphosphonium chloride, 98%   

  • 896-33-3

  • 25g

  • 232.0CNY

  • Detail
  • Alfa Aesar

  • (B23015)  Ethyltriphenylphosphonium chloride, 98%   

  • 896-33-3

  • 100g

  • 698.0CNY

  • Detail
  • Alfa Aesar

  • (B23015)  Ethyltriphenylphosphonium chloride, 98%   

  • 896-33-3

  • 500g

  • 2808.0CNY

  • Detail

896-33-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl(triphenyl)phosphonium chloride

1.2 Other means of identification

Product number -
Other names ethyl(triphenyl)phosphanium,chloride

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:896-33-3 SDS

896-33-3Relevant articles and documents

Long sought synthesis of quaternary phosphonium salts from phosphine oxides: Inverse reactivity approach

Vetter, Anna C.,Nikitin, Kirill,Gilheany, Declan G.

, p. 5843 - 5846 (2018/06/13)

Quaternary phosphonium salts (QPS), a key class of organophosphorus compounds, have previously only been available by routes involving nucleophilic phosphorus. We report the realisation of the opposite approach to QPS utilising phosphine oxides as the electrophilic partner and Grignard reagents as nucleophiles. The process is enabled through the crucial intermediacy of the derived halophosphonium salts. The route does not suffer from the slow kinetics and limited availability of many parent phosphines and a broad range of QPS were prepared in excellent yields.

One alkyl triphenyl substituted group based phosphonium salt preparation method and application

-

Paragraph 0033-0040, (2017/09/12)

The invention discloses a one alkyl triphenyl substituted group based phosphonium salt preparation method and application. The preparation method includes that a one alkyl triphenyl phosphonium salt halide I is obtained through reaction of several alkyl h

Reactions with Phosphine Alkylenes, XLII. A Sequence for the Preparation of Acetylenes Starting from Carboxylic Chlorides and Phosphorus Ylides via 1,2-Diketones.

Bestmann, Hans Juergen,Kumar, Kamlesh,Kisielowski, Lothar

, p. 2378 - 2382 (2007/10/02)

Phosphorus ylides 1 and carboxylic chlorides 2 react with transylidation to give acyl ylides 3 which are oxidized with the adduct of ozone to triphenyl phosphite to yield 1,2-diketones 5.These are converted into the bis(hydrazones) 6 which are oxidized with O2/CuCl in pyridine giving acetylenes 7.

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