431-36-7

Basic information

• Product Name: 1,1,1-TRIFLUORO-2-BUTANOL
• Synonyms: 1,1,1-TRIFLUORO-2-BUTANOL;1,1,1-Trifluorobutan-2-ol;1,1,1-Trifluorobutan-2-ol 97%;1,1,1-Trifluorobutan-2-ol97%;2-Hydroxy-1,1,1-trifluorobutane, 1-(Trifluoromethyl)propan-1-ol
• CAS NO: 431-36-7
• Molecular Formula: C₄H₇F₃O
• Molecular Weight: 128.09
• Mol File: 431-36-7.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 90.8-91.8/752mm
• Flash Point: 50.9°C
• Appearance: /
• Density: 1.166
• Refractive Index: 1.3403
• PKA: 12.53±0.20(Predicted)
• CAS DataBase Reference: 1,1,1-TRIFLUORO-2-BUTANOL(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1,1-TRIFLUORO-2-BUTANOL(431-36-7)
• EPA Substance Registry System: 1,1,1-TRIFLUORO-2-BUTANOL(431-36-7)

Safety Data

• Hazard Codes: F
• Hazardous Substances Data: 431-36-7(Hazardous Substances Data)

Usage

General Description

1,1,1-Trifluoro-2-butanol, also known as Trifluoroisobutanol, is a fluorinated alcohol compound with the chemical formula CF3CH(CHOH)CH3. It is a colorless, volatile liquid with a strong odor, and is used primarily as a solvent and as a precursor in the synthesis of pharmaceuticals and agrochemicals. It is also used in the manufacturing of polymers and as an intermediate in the production of other fluorinated compounds. This chemical is highly flammable and can cause irritation to the skin, eyes, and respiratory system, and should be handled with caution and proper protective equipment. It is important to follow safety guidelines and regulations when working with 1,1,1-Trifluoro-2-butanol to minimize potential risks to human health and the environment.

Upstream product

• 359-41-1 1,1,1-trifluoro-2,3-epoxypropane 
• 75-16-1 methylmagnesium bromide 
• 367-64-6 n-butyl trifluoroacetate 
• 925-90-6 ethylmagnesium bromide 
• 666-33-1 1,1,1-trifluoro-3-buten-2-ol 
• 431-47-0 trifluoroacetic acid-methyl ester 
• 97-93-8 triethylaluminum 
• 920-39-8 isopropylmagnesium bromide 
• 758-33-8 1,1,1-Trifluor-2-butanamin-hydrochlorid 
• 383-63-1 ethyl trifluoroacetate, 
• 381-88-4 1,1,1-trifluoro-2-butanone 

Downstream Products

• 727-27-5 4-Brom-benzolsulfonsaeure-<1-trifluormethyl-propylester> 

Relevant articles and documents

ION CHANNEL MODULATORS

The present invention is directed to, in part, fused heteroaryl compounds and compositions useful for preventing and/or treating a disease or condition relating to aberrant function of a voltage-gated, sodium ion channel, for example, abnormal late/persistent sodium current. Methods of treating a disease or condition relating to aberrant function of a sodium ion channel including neurological disorders (e.g., Dravet syndrome, epilepsy), pain, and neuromuscular disorders are also provided herein.

Study for the determination of the absolute configuration of fluoromethylated secondary alcohols by the modified Mosher method

Application of the modified Mosher method using high-field FT 1H NMR to the 2-methoxy-2-phenyl-2-trifluoromethyl acetic acid (MTPA) derivatives of fluorinated secondary alcohols indicates that this method may be generally used to determine the absolute configurations of these materials.

Deamination Reactions, 43 - The Effect of Trifluoromethyl Groups on the Reactivity of Aliphatic Diazonium Ions and Carbocations

Various trifluoroalkanamines (9, 26, 35, 38, 45, 56, and 67) have been prepared and diazotized (water, pH 3.5) to probe the effect of trifluoromethyl groups on the reactivity of aliphatic diazonium ions.The product distributions reveal that α-CF3 groups enhance inverting displacement and enforce rearrangement (hydride shifts) separating the positive charge from CF3.Migrations of the positive charge from the β- to the γ-position are less strongly promoted than those from α to β.Enhancement factors of ca. 15 (α -> β) and 4 (β -> γ) may be derived by comparison with analogous alkanediazonium ions.The positive charge does not migrate in the reverse direction (β -> α) except for minor amounts of a pinacolic rearrangement (68 -> 7).A migration of the positive charge from γ to β has been detected with 36 but a tenfold decrease as compared to the analogous butanediazonium ion 37 is indicated.All observations are reasonably explained in terms of the relative stabilities of the intermediate trifluoroalkyl cations.