1549-45-7

Basic information

• Product Name: Trifluoroacetic acid cyclohexyl
• Synonyms: Cyclohexanol trifluoroacetate;Trifluoroacetic acid cyclohexyl;Trifluoroacetic acid cyclohexyl ester;Acetic acid, 2,2,2-trifluoro-, cyclohexyl ester
• CAS NO: 1549-45-7
• Molecular Formula: C₈H₁₁F₃O₂
• Molecular Weight: 196.17
• Mol File: 1549-45-7.mol
• Article Data: 32

Chemical Properties

• Boiling Point: 147.85°C (rough estimate)
• Flash Point: 39.2°C
• Appearance: /
• Density: 1.2g/cm³
• Vapor Pressure: 1.48mmHg at 25°C
• Refractive Index: 1.398
• CAS DataBase Reference: Trifluoroacetic acid cyclohexyl(CAS DataBase Reference)
• NIST Chemistry Reference: Trifluoroacetic acid cyclohexyl(1549-45-7)
• EPA Substance Registry System: Trifluoroacetic acid cyclohexyl(1549-45-7)

Safety Data

• Hazardous Substances Data: 1549-45-7(Hazardous Substances Data)

Usage

InChI:InChI=1/C8H11F3O2/c9-8(10,11)7(12)13-6-4-2-1-3-5-6/h6H,1-5H2

Upstream product

• 407-25-0 trifluoroacetic anhydride 
• 108-93-0 cyclohexanol 
• 626-62-0 Cyclohexyl iodide 
• 2966-50-9 silver trifluoroacetate 
• 110-82-7 cyclohexane 
• 27184-84-5 chromyl trifluoroacetate 
• 76-05-1 trifluoroacetic acid 
• 542-18-7 cyclohexyl chloride 
• 110-83-8 cyclohexene 
• 96254-05-6 2-(trifluoroacetyloxy)pyridine 
• 183266-61-7 1-(trifluoroacetyl)benzotriazole 
• 201230-82-2 carbon monoxide 
• 67-68-5 dimethyl sulfoxide 
• 110-59-8 pentanonitrile 

Downstream Products

• 110-82-7 cyclohexane 
• 110-83-8 cyclohexene 
• 108-93-0 cyclohexanol 
• 1352440-92-6 cyclohexyl 2,2-difluoro-2-(trimethylsilyl)acetate 
• 1352440-95-9 C₁₄H₂₉F₃O₂Si₂ 
• 76-05-1 trifluoroacetic acid 
• 124-04-9 Adipic acid 
• 71-43-2 benzene 

Relevant articles and documents

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Selective Markovnikov's Addition of Trifluoroacetic Acid to Alkenes using Vanadium(v) Oxide

A simple and efficient method for trifluoroacetoxylation of alkenes using catalytic amounts of V2O5 in trifluoroacetic acid to give the Markovnikov's product selectively in excellent yields for the first time is described.

Synthesis and Structure of New Pt(IV) Perfluorocarboxylate Complexes and Their Reactivity with Respect to Alkanes and Cycloalkanes

New Pt(IV) perfluorocarboxylate complexes of the composition [Pt(RFCOO)4]n and M2[Pt(RFCOO)6] (RF = CF3, C2F5; M = Li, Na, K, Rb, Cs, NMe4/

Enthalpies of Hydration of Alkenes. 3. Cycloalkenes

The enthalpies of reaction of cyclopentene, cyclohexene, 1-methylcyclopentene,methylcyclohexane, methylenecyclopentane, 1-methylcyclohexene, bicyclohept-2-ene, and bicyclohex-2-ene with trifluoroacetic acid were measured.This gives the diff

METHOD FOR PRODUCING DICARBOXYLIC ACID

A method for producing dicarboxylic acid. The method includes: subjecting a raw material system including a cyclic olefin and a lower monocarboxylic acid to an addition reaction in the presence of an addition reaction catalyst to generate an intermediate product system including cyclic carboxylic acid ester; and subjecting the intermediate product system including cyclic carboxylic acid ester to a ring-opening and oxidation reaction in the presence of an oxidant and an oxidation catalyst to generate a corresponding dicarboxylic acid product. The addition reaction in the dicarboxylic acid synthesis route achieves a high single-pass conversion rate, and the selectivity of the corresponding cyclic carboxylic acid ester is high. The addition-oxidation synthesis route achieves faster reaction rates for both the addition reaction and oxidation reaction, and high yield of corresponding dicarboxylic acid product. The addition-oxidation based synthesis route is suitable for continuous, stable and large-scale production of corresponding dicarboxylic acid product.