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Catalog Number:
45433
CAS Number:
389-31-1
2-Fluoro-DL-mandelic acid
Purity:
≥ 98% (GC)
Synonym(s):
2-(2-Fluorophenyl)-2-hydroxyacetic acid
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$156.43 /5G
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Product Information

2-Fluoro-DL-mandelic acid is a versatile compound recognized for its unique fluorinated structure, which enhances its reactivity and potential applications in various fields. This compound is particularly valuable in the pharmaceutical industry, where it serves as a key intermediate in the synthesis of various drugs, including those targeting metabolic disorders and certain types of cancer. Its ability to act as a chiral building block allows researchers to develop enantiomerically pure compounds, which are crucial for the efficacy and safety of pharmaceutical products.

In addition to its pharmaceutical applications, 2-Fluoro-DL-mandelic acid is also utilized in the development of agrochemicals and as a reagent in organic synthesis. Its distinctive properties make it an attractive option for researchers looking to innovate in drug development and chemical synthesis. With its growing relevance in medicinal chemistry and organic synthesis, this compound stands out as a valuable resource for professionals seeking to enhance their research and product development efforts.

Synonyms
2-(2-Fluorophenyl)-2-hydroxyacetic acid
CAS Number
389-31-1
Purity
≥ 98% (GC)
Molecular Formula
C8H7FO3
Molecular Weight
170.14
MDL Number
MFCD03095382
PubChem ID
2783169
Melting Point
115 - 119 °C
Appearance
White to almost white powder to crystal
Boiling Point
72 °C/0.2 mmHg
Conditions
Store at RT
General Information
Synonyms
2-(2-Fluorophenyl)-2-hydroxyacetic acid
CAS Number
389-31-1
Purity
≥ 98% (GC)
Molecular Formula
C8H7FO3
Molecular Weight
170.14
MDL Number
MFCD03095382
PubChem ID
2783169
Melting Point
115 - 119 °C
Appearance
White to almost white powder to crystal
Boiling Point
72 °C/0.2 mmHg
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-Fluoro-DL-mandelic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in designing drugs that target specific biological pathways.
  • Analytical Chemistry: It is used as a standard in analytical methods, such as chromatography, to ensure accurate measurement of similar compounds in complex mixtures.
  • Biochemical Research: Researchers employ it to study enzyme interactions and metabolic pathways, providing insights into drug metabolism and efficacy.
  • Cosmetic Formulations: Its properties make it suitable for use in skincare products, where it can help in skin brightening and improving overall skin texture.
  • Fluorine Chemistry: The presence of fluorine enhances the compound's stability and bioavailability, making it valuable in the development of fluorinated compounds for various applications.

Citations