433-25-0 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
Describes the appearance and state of the compound at room temperature.
Explanation
1,3-Butanediol, 4,4,4-trifluorois a derivative of butanediol, meaning it is structurally related and has been modified from the original compound.
Explanation
The compound contains three fluorine atoms, which differentiate it from other butanediol derivatives.
Explanation
The compound is used in the production of various industrial and consumer products, including those in the pharmaceutical, polymer, and plastic industries.
Explanation
1,3-Butanediol, 4,4,4-trifluorois used as a solvent, which means it can dissolve other substances and facilitate chemical reactions.
Explanation
The compound serves as a starting material for the synthesis of other organic compounds, making it a versatile building block in chemical reactions.
Explanation
Although the compound has a relatively low toxicity, it can still cause harm if not handled properly.
Explanation
Prolonged exposure to 1,3-Butanediol, 4,4,4-trifluoromay cause irritation to the skin and eyes, as well as potential respiratory and digestive issues.
Explanation
When working with 1,3-Butanediol, 4,4,4-trifluoro-, it is essential to follow proper handling and safety precautions to minimize the risk of exposure and potential health hazards.
Physical state
Colorless, odorless liquid
Derivative
Butanediol
Fluorine content
Three fluorine atoms
Applications
Pharmaceutical, polymer, and plastic production
Use as a solvent
Solvent properties
Synthesis
Starting material for other organic compounds
Toxicity
Relatively low toxicity
Health hazards
Skin and eye irritation, potential respiratory and digestive issues
Safety precautions
Proper handling and safety measures required
Check Digit Verification of cas no
The CAS Registry Mumber 433-25-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,3 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 433-25:
(5*4)+(4*3)+(3*3)+(2*2)+(1*5)=50
50 % 10 = 0
So 433-25-0 is a valid CAS Registry Number.
433-25-0Relevant articles and documents
The fluorine-containing α, β - production of unsaturated aldehydes
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Paragraph 0088; 0095, (2017/09/26)
The purpose of the present invention is to provide a fluorine-containing alpha,beta-unsaturated aldehyde, a method for producing same, an optically active fluorine-containing compound using the fluorine-containing alpha,beta-unsaturated aldehyde, and a method for producing same. This method for producing a fluorine-containing alpha,beta-unsaturated aldehyde is a method for producing a fluorine-containing alpha,beta-unsaturated aldehyde represented by formula (1) and comprises: an oxidizing step of oxidizing an alcohol represented by formula (2) in a high-boiling-point solvent, which has a higher boiling point than the corresponding alpha,beta-unsaturated aldehyde, by using an oxidizing agent that is insoluble to the high-boiling-point solvent; and a purifying step of purifying the reaction solution obtained in the oxidizing step by distillation. In formulae (1) and (2), R1 and R2 each independently represent a hydrogen atom or a fluorine atom, and X is 2 or 3.
Process for producing 4,4,4,- trifluoro-3-hydroxybutyric acid
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, (2008/06/13)
A first process for producing an optically active perfluoroalkylcarbinol derivative includes (a) reacting an optically active imine with a compound that is a hemiacetal of a perfluoroalkylaldehyde or a hydrate of a perfluoroalkylaldehyde to obtain a conde
Stereoselective Preparation of Ethyl 2,3-Dihydroxy-4,4,4-trifluorobutyrates via Enzymatic Optical Resolution
Yamazaki, Takashi,Okamura, Naoko,Kitazume, Tomoya
, p. 521 - 524 (2007/10/02)
Ethyl 2,3-dihydroxy-4,4,4-trifluorobutyrate was prepared in a highly diastereo- as well as enantioselective manner via enzymatic optical resolution followed by chemical transformations with complete retention of their configurations.
