(E)-3-(2-fluoro-4-hydroxyphenyl)acrylic acid, also known as 2-Fluoro-4-hydroxycinnamic acid, is a chemical compound with the molecular formula C9H7FO3. It is a derivative of cinnamic acid and is classified as a phenolic acid. (E)-3-(2-fluoro-4-hydroxyphenyl)acrylic acid is characterized by its unique structure and properties, which make it a versatile molecule for various applications in the fields of chemistry and pharmacology.
696589-23-8
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Basic information
- Product Name: (E)-3-(2-fluoro-4-hydroxyphenyl)acrylic acid
- Synonyms: (E)-3-(2-fluoro-4-hydroxyphenyl)acrylic acid
- CAS NO:696589-23-8
- Molecular Formula: C9H7FO3
- Molecular Weight: 182.15
- EINECS: N/A
- Product Categories: N/A
- Mol File: 696589-23-8.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: /
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: (E)-3-(2-fluoro-4-hydroxyphenyl)acrylic acid(CAS DataBase Reference)
- NIST Chemistry Reference: (E)-3-(2-fluoro-4-hydroxyphenyl)acrylic acid(696589-23-8)
- EPA Substance Registry System: (E)-3-(2-fluoro-4-hydroxyphenyl)acrylic acid(696589-23-8)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 696589-23-8(Hazardous Substances Data)
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696589-23-8 Usage
Uses
Used in Pharmaceutical Research:(E)-3-(2-fluoro-4-hydroxyphenyl)acrylic acid is used as an intermediate in the synthesis of pharmaceutical drugs for its potential therapeutic effects. Its unique structure allows for the development of new drugs with improved efficacy and reduced side effects.
Used in Chemical Research:
In the field of chemical research, (E)-3-(2-fluoro-4-hydroxyphenyl)acrylic acid is used as a starting material for the synthesis of other organic compounds. Its reactivity and structural features make it a valuable component in the creation of novel chemical entities.
Used in Material Science:
(E)-3-(2-fluoro-4-hydroxyphenyl)acrylic acid has potential applications in the development of new materials due to its unique structure and properties. It can be utilized in the creation of advanced materials with specific characteristics, such as improved stability or enhanced bioactivity.
Used in Bioactive Compound Development:
(E)-3-(2-fluoro-4-hydroxyphenyl)acrylic acid's structure and properties also make it a promising candidate for the development of bioactive compounds. (E)-3-(2-fluoro-4-hydroxyphenyl)acrylic acid can be used as a building block in the design and synthesis of new bioactive molecules with potential applications in medicine and biotechnology.
Overall, (E)-3-(2-fluoro-4-hydroxyphenyl)acrylic acid is a versatile and valuable compound with a wide range of potential uses and applications in the fields of chemistry, pharmacology, material science, and bioactive compound development. Its unique structure and properties make it an important molecule for research and development efforts in these areas.
Check Digit Verification of cas no
The CAS Registry Mumber 696589-23-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,6,5,8 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.Calculate Digit Verification of CAS Registry Number 696589-23:
(8*6)+(7*9)+(6*6)+(5*5)+(4*8)+(3*9)+(2*2)+(1*3)=238
238 % 10 = 8
So 696589-23-8 is a valid CAS Registry Number.
696589-23-8Upstream product
696589-23-8Downstream Products
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(E)-3-(2-fluoro-4-hydroxyphenyl)acrylic acid
