Phenyl-1,3,5-triazine | CAS No. 1722-18-5

Phenyl-1,3,5-triazine

Basic Information

CAS Number

1722-18-5

Molecular Formula

C9H7N3

Molecular Weight

157.17 g/mol

AD

Basic Physical Properties

Boiling Point

341.8 °C at 760 mmHg

Density

1.169

Flash Point

163.7 °C

Refractive Index

1.586

C1=CC=C(C=C1)C2=NC=NC=N2

InChI

InChI=1S/C9H7N3/c1-2-4-8(5-3-1)9-11-6-10-7-12-9/h1-7H

InChIKey

RXELBMYKBFKHSM-UHFFFAOYSA-N

LogP

1.53860

Complexity

126

Synonyms & References

English

  • AKOS015899580
  • 1,3,5-Triazine, 2-phenyl- (9CI)
  • 1722-18-5
  • SCHEMBL36826
  • 2-phenyl-[1,3,5]triazine
  • AM808273
  • PHENYL-1,3,5-TRIAZINE
  • 2-phenyl-sym-triazine
  • DTXSID30274555
  • InChI=1/C9H7N3/c1-2-4-8(5-3-1)9-11-6-10-7-12-9/h1-7
  • 1,3,5-triazine, 2-phenyl-
  • 2-phenyl-1,3,5-triazine
  • 2-Phenyl-s-triazine
  • 1,3,5-triazine,2-phenyl
  • Phenyl-[1,3,5]triazin
  • phenyl-[1,3,5]triazine

MDL Number

MFCD16619132

Customs Code

2933699090

FAQ

What are the physical and chemical properties of Phenyl-1,3,5-triazine (CAS: 1722-18-5)?

Phenyl-1,3,5-triazine (CAS: 1722-18-5) is a white crystalline solid with a molecular weight of approximately 206.21 g/mol. It is slightly soluble in water but more soluble in organic solvents like ethanol and acetone. The compound is known for its stability and limited reactivity, making it suitable for various applications. It is also known for its low volatility and melting point of about 220°C.

How is Phenyl-1,3,5-triazine (CAS: 1722-18-5) typically synthesized?

Phenyl-1,3,5-triazine is typically synthesized by the condensation of phenyl isocyanate with urea. The reaction is catalyzed by acid or base conditions and proceeds with good yield. The process involves careful control of temperature and reaction time to achieve the desired product with high purity and selectivity.

What industries use Phenyl-1,3,5-triazine (CAS: 1722-18-5)?

Phenyl-1,3,5-triazine (CAS: 1722-18-5) is used in a variety of industries. It is utilized in the pharmaceutical industry as a precursor for certain medications, in the polymer industry for its stabilizing properties, and in the semiconductor industry for its ability to act as a dopant. Additionally, it finds applications in the production of sensors and other electronic devices.

What precautions should be taken when handling Phenyl-1,3,5-triazine (CAS: 1722-18-5)?

When handling Phenyl-1,3,5-triazine (CAS: 1722-18-5), it is important to use personal protective equipment (PPE) such as gloves, goggles, and a lab coat. The compound should be stored in a cool, dry place away from direct sunlight and sources of heat. In case of a spill, it should be contained and disposed of according to local regulations. Always refer to the Safety Data Sheet (SDS) for detailed handling and emergency procedures.

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