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Triphenylphosphineimine hemisulfate salt is a chemical compound that consists of triphenylphosphineimine and hemisulfate. Triphenylphosphineimine is an organic compound with a phosphorus atom bonded to three phenyl groups and a nitrogen atom. It is known for its role as a ligand in coordination chemistry and as a reagent in organic synthesis. The hemisulfate salt form of triphenylphosphineimine is characterized by its white or light yellow crystalline appearance and its solubility in water and ethanol. Triphenylphosphineimine hemisulfate salt finds utility in a variety of applications, including the production of pharmaceuticals, agrochemicals, and other industrial processes, as well as in the synthesis of coordination complexes and as a catalyst in organic reactions.

109724-97-2

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109724-97-2 Usage

Uses

Used in Pharmaceutical Production:
Triphenylphosphineimine hemisulfate salt is used as a reagent in the synthesis of various pharmaceutical compounds. Its unique chemical properties allow it to facilitate specific reactions that are crucial for the production of certain medications.
Used in Agrochemical Production:
In the agrochemical industry, triphenylphosphineimine hemisulfate salt is utilized as a component in the creation of pesticides and other agricultural chemicals. Its role in these processes helps to ensure the effectiveness and quality of the final products.
Used in Industrial Processes:
Triphenylphosphineimine hemisulfate salt is employed in a range of industrial applications, where its chemical properties contribute to the manufacturing of various products. Its versatility in chemical reactions makes it a valuable component in these processes.
Used in Synthesis of Coordination Complexes:
As a ligand in coordination chemistry, triphenylphosphineimine hemisulfate salt is used in the synthesis of coordination complexes. These complexes have applications in areas such as catalysis, materials science, and supramolecular chemistry.
Used as a Catalyst in Organic Reactions:
Triphenylphosphineimine hemisulfate salt is also used as a catalyst to accelerate organic reactions. Its ability to lower the activation energy of certain reactions makes it an efficient and valuable tool in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 109724-97-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,7,2 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 109724-97:
(8*1)+(7*0)+(6*9)+(5*7)+(4*2)+(3*4)+(2*9)+(1*7)=142
142 % 10 = 2
So 109724-97-2 is a valid CAS Registry Number.

109724-97-2 Well-known Company Product Price

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  • Aldrich

  • (SYX00009)  Triphenylphosphineimine hemisulfate salt  AldrichCPR

  • 109724-97-2

  • SYX00009-1G

  • 1,290.51CNY

  • Detail

109724-97-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Imino(triphenyl)phosphorane

1.2 Other means of identification

Product number -
Other names -

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:109724-97-2 SDS

109724-97-2Upstream product

109724-97-2Downstream Products

109724-97-2Relevant academic research and scientific papers

Asymmetric Catalytic 1,2-Hydroperoxidation of Isatin-Derived Ketimine with Hydrogen Peroxide in the Crowding Environment of PEGs

Guo, Wengang,Liu, Yan,Li, Can

supporting information, p. 1044 - 1047 (2017/03/15)

The first enantioselective catalytic 1,2-hydroperoxidation has been achieved in the presence of PEG-600 using an acid-base bifunctional chiral squaramide as the organocatalyst, affording a range of enantioenriched α-N-substituted hydroperoxides bearing an

Oxaziridine-mediated amination of primary amines: Scope and application to a one-pot pyrazole synthesis

Armstrong, Alan,Jones, Lyn H.,Knight, Jamie D.,Kelsey, Richard D.

, p. 713 - 716 (2007/10/03)

(Chemical Equation Presented) Electrophilic amination of primary aliphatic and aromatic amines is reported using a diethylketomalonate-derived oxaziridine to afford the corresponding N-Boc hydrazines in good to excellent yields. The method allows a one-pot synthesis of pyrazoles from primary amines.

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