What is the CAS number for 1-phenylaziridine?

The CAS number of 1-phenylaziridine is 696-18-4.

What is 1-phenylaziridine (696-18-4) used for?

1-Phenylaziridine, also known as phenylaziridine or 2-phenylaziridine, is an organic compound characterized by its molecular formula C8H9N. It is a cyclic amine with a strained three-membered aziridine ring that features a phenyl group attached to the nitrogen atom. As a colorless liquid at room temperature, 1-phenylaziridine is highly reactive, making it a valuable building block in organic synthesis for the creation of pharmaceuticals, agrochemicals, and other fine chemicals. It also serves as a reagent in the synthesis of chiral ligands and catalysts for asymmetric catalysis. However, due to its potential health hazards and irritant properties, careful handling and use are essential.InChI:InChI=1/C8H9N/c1-2-4-8(5-3-1)9-6-7-9/h1-5H,6-7H2

What is the CAS number for 1-phenylaziridine?

The CAS number of 1-phenylaziridine is 696-18-4.

What is 1-phenylaziridine (696-18-4) used for?

1-Phenylaziridine, also known as phenylaziridine or 2-phenylaziridine, is an organic compound characterized by its molecular formula C8H9N. It is a cyclic amine with a strained three-membered aziridine ring that features a phenyl group attached to the nitrogen atom. As a colorless liquid at room temperature, 1-phenylaziridine is highly reactive, making it a valuable building block in organic synthesis for the creation of pharmaceuticals, agrochemicals, and other fine chemicals. It also serves as a reagent in the synthesis of chiral ligands and catalysts for asymmetric catalysis. However, due to its potential health hazards and irritant properties, careful handling and use are essential.InChI:InChI=1/C8H9N/c1-2-4-8(5-3-1)9-6-7-9/h1-5H,6-7H2

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1-phenylaziridine

Q: What is the 1-phenylaziridine?

1-phenylaziridine is , while it's Molecular Formula is C8H9 N. Used in Organic Synthesis: 1-Phenylaziridine is used as a building block for the synthesis of various pharmaceuticals, agrochemicals, and other fine chemicals, leveraging its reactivity and structural properties to create a wide range of compounds. Used in Chiral Ligand and Catalyst Synthesis: 1-Phenylaziridine is utilized as a reagent in the synthesis of chiral ligands and catalysts for asymmetric catalysis, contributing to the development of enantioselective reactions and the production of enantiomerically pure compounds. Used in Research and Development: In the scientific community, 1-phenylaziridine serves as a valuable research tool for exploring new reaction pathways and developing innovative synthetic methods, further expanding its applications in the field of chemistry.

CAS：696-18-4
purity：99%

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Details

99% Purity Commercial production 1-phenylaziridine 696-18-4 with Cheapest Price

Molecular Formula:C8H9 N
Molecular Weight:119.166
Vapor Pressure:0.422mmHg at 25°C
Boiling Point:195.3°C at 760 mmHg
Flash Point:64.4°C
PSA：3.01000
Density:1.098g/cm³
LogP:1.57160

1-phenylaziridine(Cas 696-18-4) Usage

General Description

1-Phenylaziridine, also known as phenylaziridine or 2-phenylaziridine, is an organic compound with the molecular formula C8H9N. It is a cyclic amine with a three-membered aziridine ring that contains a phenyl group attached to the nitrogen atom. 1-Phenylaziridine is a colorless liquid at room temperature and is highly reactive due to the strain in the aziridine ring. It is primarily used as a building block in organic synthesis, where it serves as a versatile precursor for various pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, 1-phenylaziridine is also used as a reagent in the synthesis of chiral ligands and catalysts for asymmetric catalysis. However, it is important to handle and use 1-phenylaziridine with caution due to its potential health hazards and irritant properties.

InChI:InChI=1/C8H9N/c1-2-4-8(5-3-1)9-6-7-9/h1-5H,6-7H2

696-18-4 Relevant articles

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Heine,Kapur

, p. 4892 (1955)

Cationic N-substituted aniline ionic liquid and preparation method thereof

-

Paragraph 0089-0097, (2020/05/14)

The invention discloses a cationic N-sub...

Formation of azomethine ylids by thermolysis of oxazolidines. Study of the reaction in solution and in the gaseous phase

Bureau, R.,Mortier, J.,Joucla, M.

, p. 584 - 596 (2007/10/02)

Thermolysis of oxazolidines leads to azo...

Substituted amine derivatives, their production and use

-

, (2008/06/13)

Substituted amino derivatives represente...

Organoboranes for synthesis. Reaction of organoboranes with representative organic azides. A general stereospecific synthesis of secondary amines and N-substituted aziridines

Brown, Herbert C.,Midland, M.Mark,Levy, Alan B.,Brown,Wetherill,Suzuki, Akira,Sono, Sunao,Itoh, Mitsuomi

, p. 4079 - 4088 (2007/10/02)

Reaction of trialkylboranes with organic...

696-18-4 Process route

: 122-98-5
2-Anilinoethanol

: 696-18-4
1-phenylaziridine

Conditions

Conditions	Yield
With 1 M DTPP; at 60 ℃; for 48h;	90%
Multi-step reaction with 2 steps 1: 85 percent / toluene / 12 h / Heating 2: 23 percent / gas / 550 °C / 0.02 Torr In toluene;
With triethylamine; triphenylphosphine; In tetrachloromethane; acetonitrile;