(S)-3-amino-4,4,4-trifluorobutanoic acid, with the molecular formula C4H7F3NO2, is a chiral amino acid derivative of the natural amino acid alanine. It is characterized by the replacement of one hydrogen atom with a trifluoromethyl group, which imparts unique properties to the molecule. (S)-3-amino-4,4,4-trifluorobutanoic acid is widely recognized for its applications in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals, as well as in the development of novel materials and as a ligand in catalytic processes.
151871-99-7
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Basic information
- Product Name: (S)-3-amino-4,4,4-trifluorobutanoic acid
- Synonyms: (S)-3-amino-4,4,4-trifluorobutanoic acid
- CAS NO:151871-99-7
- Molecular Formula:
- Molecular Weight: 157.092
- EINECS: N/A
- Product Categories: N/A
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: N/A
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: (S)-3-amino-4,4,4-trifluorobutanoic acid(CAS DataBase Reference)
- NIST Chemistry Reference: (S)-3-amino-4,4,4-trifluorobutanoic acid(151871-99-7)
- EPA Substance Registry System: (S)-3-amino-4,4,4-trifluorobutanoic acid(151871-99-7)
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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: 151871-99-7(Hazardous Substances Data)
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151871-99-7 Usage
Uses
Used in Pharmaceutical Synthesis:(S)-3-amino-4,4,4-trifluorobutanoic acid is used as a building block for the development of new pharmaceuticals. Its unique properties, including the presence of the trifluoromethyl group, make it a valuable component in the creation of innovative drugs with enhanced efficacy and selectivity.
Used in Agrochemical Development:
In the agrochemical industry, (S)-3-amino-4,4,4-trifluorobutanoic acid is utilized as a key component in the synthesis of novel agrochemicals. Its introduction into the molecular structure can lead to the development of more effective and targeted pesticides, herbicides, and other agricultural products.
Used in Fine Chemicals Production:
(S)-3-amino-4,4,4-trifluorobutanoic acid is also employed in the production of fine chemicals, which are high-purity chemicals used in various applications, including the fragrance, flavor, and specialty chemical industries. Its unique properties contribute to the creation of high-quality and specialized products.
Used in Novel Material Development:
(S)-3-amino-4,4,4-trifluorobutanoic acid is used as a building block in the development of novel materials, where its unique properties can be leveraged to create materials with specific characteristics, such as improved stability, reactivity, or selectivity.
Used as a Ligand in Catalytic Processes:
(S)-3-amino-4,4,4-trifluorobutanoic acid is utilized as a ligand in catalytic processes, where it can enhance the efficiency and selectivity of chemical reactions. Its unique properties make it a valuable tool in the development of new catalysts for various industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 151871-99-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,8,7 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.Calculate Digit Verification of CAS Registry Number 151871-99:
(8*1)+(7*5)+(6*1)+(5*8)+(4*7)+(3*1)+(2*9)+(1*9)=147
147 % 10 = 7
So 151871-99-7 is a valid CAS Registry Number.
151871-99-7Upstream product
151871-99-7Downstream Products
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(S)-3-amino-4,4,4-trifluorobutanoic acid
