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62942-43-2

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62942-43-2 Usage

Chemical Properties

YELLOW POWDER

Uses

Different sources of media describe the Uses of 62942-43-2 differently. You can refer to the following data:
1. Reactant for:? ;Hydroazidation reactions in preparation of a-azido alcohols1? ;Preparation of prodrug (2-hydroxyamino-vinyl)-triphenyl-phosphonium (HVTP) inhibitor of peroxidase activity and apoptosis2? ;Intramolecular [4 + 3] cycloaddition reactions3
2. (Formylmethyl)triphenylphosphonium Chloride is a useful Wittig reagent. Used as a reactant for Hydroazidation reactions in preparation of a-azido alcohols, Preparation of prodrug (2-hydroxyamino-vinyl)-triphenyl-phosphonium (HVTP) inhibitor of peroxidase activity and apoptosis and Intramolecular [4 + 3] cycloaddition reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 62942-43-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,9,4 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 62942-43:
(7*6)+(6*2)+(5*9)+(4*4)+(3*2)+(2*4)+(1*3)=132
132 % 10 = 2
So 62942-43-2 is a valid CAS Registry Number.
InChI:InChI=1/C20H18OP.ClH/c21-16-17-22(18-10-4-1-5-11-18,19-12-6-2-7-13-19)20-14-8-3-9-15-20;/h1-16H,17H2;1H/q+1;

62942-43-2 Well-known Company Product Price

  • Brand
  • (Code)Product description
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  • Detail
  • TCI America

  • (F0331)  (Formylmethyl)triphenylphosphonium Chloride  >98.0%(T)

  • 62942-43-2

  • 5g

  • 260.00CNY

  • Detail
  • TCI America

  • (F0331)  (Formylmethyl)triphenylphosphonium Chloride  >98.0%(T)

  • 62942-43-2

  • 25g

  • 740.00CNY

  • Detail
  • Alfa Aesar

  • (A15733)  (Formylmethyl)triphenylphosphonium chloride, 98+%   

  • 62942-43-2

  • 10g

  • 299.0CNY

  • Detail
  • Alfa Aesar

  • (A15733)  (Formylmethyl)triphenylphosphonium chloride, 98+%   

  • 62942-43-2

  • 50g

  • 1252.0CNY

  • Detail
  • Alfa Aesar

  • (A15733)  (Formylmethyl)triphenylphosphonium chloride, 98+%   

  • 62942-43-2

  • 100g

  • 2247.0CNY

  • Detail
  • Aldrich

  • (47718)  (Formylmethyl)triphenylphosphoniumchloride  ≥97.0% (AT)

  • 62942-43-2

  • 47718-10G

  • 458.64CNY

  • Detail

62942-43-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (FORMYLMETHYL)TRIPHENYLPHOSPHONIUM CHLORIDE

1.2 Other means of identification

Product number -
Other names 2-oxoethyl(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:62942-43-2 SDS

62942-43-2Relevant articles and documents

Method for preparing formyl methylene triphenylphosphine

-

, (2020/12/14)

The invention discloses a method for preparing formyl methylene triphenylphosphine. The method comprises the following steps: reacting triphenylphosphine with excessive chloroacetaldehyde dimethyl acetal under the catalysis of a proper catalyst to obtain corresponding quaternary phosphonium salt; dissolving quaternary phosphonium salt in water, adding a trace amount of inorganic acid to hydrolyzethe quaternary phosphonium salt, dropwise adding the hydrolyzed quaternary phosphonium salt into an aqueous solution of alkali according to a conventional method, and filtering and washing precipitates to directly obtain formyl methylene triphenylphosphine. The method has the advantages of no use of expensive reagents, simple operation, high yield, less three wastes, and easy realization of industrialization.

Synthesis of Polysubstituted Pyridines via a One-Pot Metal-Free Strategy

Wei, Hongbo,Li, Yun,Xiao, Ke,Cheng, Bin,Wang, Huifei,Hu, Lin,Zhai, Hongbin

supporting information, p. 5974 - 5977 (2016/01/09)

An efficient strategy for the one-pot synthesis of polysubstituted pyridines via a cascade reaction from aldehydes, phosphorus ylides, and propargyl azide is reported. The reaction sequence involves a Wittig reaction, a Staudinger reaction, an aza-Wittig reaction, a 6π-3-azatriene electrocyclization, and a 1,3-H shift. This protocol provides quick access to the polysubstituted pyridines from readily available substrates in good to excellent yields.

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