4-Phenyl-1,3-thiazole-2-carbaldehyde | CAS No. 75390-44-2

4-Phenyl-1,3-thiazole-2-carbaldehyde

Basic Information

CAS Number

75390-44-2

Molecular Formula

C10H7NOS

Molecular Weight

189.24 g/mol

AD

Basic Physical Properties

C1=CC=C(C=C1)C2=CSC(=N2)C=O

InChI

InChI=1S/C10H7NOS/c12-6-10-11-9(7-13-10)8-4-2-1-3-5-8/h1-7H

InChIKey

DJWIXPPOXVIXSZ-UHFFFAOYSA-N

LogP

2.6226000000000003

Topological Polar Surface Area

29.96 Ų

Hydrogen Bond Donor/Acceptor

0 / 2

Complexity

180

Synonyms & References

English

  • CS-0156391
  • FT-0691870
  • EN300-65675
  • SY106868
  • D82945
  • 4-PHENYL-THIAZOLE-2-CARBALDEHYDE
  • 75390-44-2
  • BB 0249283
  • 4-phenyl-1,3-thiazole-2-carbaldehyde, AldrichCPR
  • Z1021388612
  • SCHEMBL2224538
  • 4-phenyl-1,3-thiazole-2-carbaldehyde
  • 4-Phenylthiazole-2-carbaldehyde
  • 4-phenyl-2-thiazolecarboxaldehyde
  • A838399
  • 4-phenyl-1,3-thiazole-2-carboxaldehyde
  • AB12112
  • MFCD02665589
  • AKOS001476298
  • AS-60499
  • DJWIXPPOXVIXSZ-UHFFFAOYSA-N
  • 2-formyl-4-phenylthiazole
  • DTXSID20393446
  • 2-Thiazolecarboxaldehyde,4-phenyl-
  • 4-PHENYL-1,3-THIAZOLE-2-CARBALDEHYDE
  • 4-phenyl-1,3-thiazole-2-carbaldehyde(SALTDATA: FREE)
  • 4-Phenyl-2-Thiazolecarboxaldehyde
  • 4-Phenyl-thiazol-2-carbaldehyd
  • BBL020795
  • 2-Thiazolecarboxaldehyde, 4-phenyl-
  • STK893485

MDL Number

MFCD02665589

Customs Code

2934100090

FAQ

What are the physical and chemical properties of 4-Phenyl-1,3-thiazole-2-carbaldehyde (CAS: 75390-44-2)?

4-Phenyl-1,3-thiazole-2-carbaldehyde is a crystalline solid with a molecular weight of approximately 218.23 g/mol. It has a low solubility in water but is more soluble in organic solvents like ethanol and acetone. The compound exhibits good reactivity towards nucleophiles and is susceptible to electrophilic substitution reactions. It is also noted for its ability to form stable complexes with metal ions.

How is 4-Phenyl-1,3-thiazole-2-carbaldehyde (CAS: 75390-44-2) typically synthesized?

4-Phenyl-1,3-thiazole-2-carbaldehyde can be synthesized via the condensation of 1,3-thiazole-2-carbaldehyde and phenylisocyanide using a base like sodium hydride. The reaction yields a high purity product with good selectivity and a good yield of up to 85%. Chromatographic techniques such as silica gel column chromatography can be used for purification.

What industries use 4-Phenyl-1,3-thiazole-2-carbaldehyde (CAS: 75390-44-2)?

4-Phenyl-1,3-thiazole-2-carbaldehyde finds application in the pharmaceutical industry for the synthesis of drugs, particularly those targeting anti-inflammatory and anti-tumor activities. It is also used in the polymer industry as a monomer for the production of functionalized polymers. Additionally, it has applications in the development of sensors and materials for their electronics and semiconductor industries.

What precautions should be taken when handling 4-Phenyl-1,3-thiazole-2-carbaldehyde (CAS: 75390-44-2)?

Proper handling of 4-Phenyl-1,3-thiazole-2-carbaldehyde requires the use of personal protective equipment such as gloves, goggles, and a lab coat. This compound should be handled in a fume hood to avoid inhalation. Spills should be cleaned up using appropriate absorbent materials, and the area should be well-ventilated. Safety data sheets (SDS) should be consulted for detailed emergency response procedures and storage recommendations.

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