Welcome to LookChem.com Sign In|Join Free
  • or
Iodure de triphenyl N-isopropylaminophosphonium, also known as triphenyl(isopropyl)phosphonium iodide, is a chemical compound with the formula (C6H5)3P(NHC3H7)I. It is a salt derived from triphenylphosphine and isopropylamine, featuring a phosphonium cation and an iodide anion. iodure de triphenyl N-isopropylaminophosphonium is often used as a phase-transfer catalyst in organic synthesis, facilitating reactions between organic and inorganic compounds. It is also employed in the preparation of various organophosphorus compounds and as a reagent in the synthesis of pharmaceuticals. The compound is typically a white crystalline solid and is sensitive to moisture, requiring storage under anhydrous conditions.

900-94-7

Post Buying Request

900-94-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

900-94-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 900-94-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,0 and 0 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 900-94:
(5*9)+(4*0)+(3*0)+(2*9)+(1*4)=67
67 % 10 = 7
So 900-94-7 is a valid CAS Registry Number.

900-94-7Downstream Products

900-94-7Relevant academic research and scientific papers

L'AZA-YLURE N-LITHIE (C6H5)3P=NLi, REACTIF D'AMINATION

Cristau, H. J.,Chiche, L.,Kadoura, J.,Torreilles, E.

, p. 3931 - 3934 (1988)

The preparation of the lithiated aza-ylide 3 has been improved and its one-pot reactivity toward alkyl and acyl halides to give amino-phosphonium salts and accordingly amines is described.

Alkylation et acylation de la triphenylphosphinimine N-lithiee

Cristau, Henri-Jean,Kadoura, Jumaah,Chiche, Laurent,Torreilles, Eliane

, p. 515 - 520 (2007/10/02)

A new synthetic approach to primary and secondary amines using N-lithiated triphenylphosphinimine is reported.This key reagent, accessible in two steps from dibromortiphenylphosphorane and ammonia, when treated with electrophiles yields N-substituted triphenylphosphinimine derivatives.These can react to give N-mono or disubstituted triphenylphosphonium salts which upon hydrolysis lead to the corresponding primary and secondary amines.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 900-94-7