4162-55-4

Basic information

• Product Name: 3-TRIFLUOROMETHYL-PENTANEDIOIC ACID
• Synonyms: 3-TRIFLUOROMETHYL-PENTANEDIOIC ACID
• CAS NO: 4162-55-4
• Molecular Formula: C₆H₇F₃O₄
• Molecular Weight: 200.1125896
• Mol File: 4162-55-4.mol
• Article Data: 5

Chemical Properties

• Melting Point: 104 °C
• Boiling Point: 284.5±35.0 °C(Predicted)
• Appearance: /
• Density: 1.497±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 3.66±0.10(Predicted)
• CAS DataBase Reference: 3-TRIFLUOROMETHYL-PENTANEDIOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 3-TRIFLUOROMETHYL-PENTANEDIOIC ACID(4162-55-4)
• EPA Substance Registry System: 3-TRIFLUOROMETHYL-PENTANEDIOIC ACID(4162-55-4)

Safety Data

• Hazardous Substances Data: 4162-55-4(Hazardous Substances Data)

Usage

General Description

3-Trifluoromethyl-pentanedioic acid, also known as TFPD, is a fluorinated organic compound with the chemical formula C7H9F3O4. It is used in the synthesis of pharmaceuticals and agrochemicals and is also used as a building block in organic chemistry. TFPD is a white crystalline solid with a high melting point and is soluble in water. It is a relatively stable compound and is not known to be highly reactive or hazardous. Despite its low reactivity, TFPD is classified as a harmful substance and should be handled with care.

InChI:InChI=1S/C6H7F3O4/c7-6(8,9)3(1-4(10)11)2-5(12)13/h3H,1-2H2,(H,10,11)(H,12,13)

Upstream product

• 138852-02-5 diethyl 3-(trifluoromethyl)pentanedioate 
• 25597-16-4 ethyl 4,4,4-trifluorocrotonate 
• 105-53-3 diethyl malonate 
• 853644-35-6 α,α'-dicyano-β-trifluoromethylglutamide 
• 75-90-1 2,2,2-Trifluoroacetaldehyde 
• 107-91-5 cyanoacetic acid amide 
• 1841-65-2 3-Trifluormethyl-glutarsaeure-dianilid 

Downstream Products

• 39890-98-7 2,6-dichloro-4-(trifluoromethyl)pyridine 

Relevant articles and documents

Stereoselective aldol reaction of glutarimides using pseudo C2 symmetry

(Figure presented) The boron aldol reaction of β-substituted glutaric imldes bearing an oxazolidinone-based auxiliary proceeds with excellent diastereoselectivity; switching the tertiary amine employed between /-Pr 2EtN or Et3N affor

Synthesis of novel analogues of marine indole alkaloids: Mono(indolyl)-4-trifluoromethylpyridines and bis(indolyl)-4-trifluoromethylpyridines as potential anticancer agents

Mono(indolyl)-4-trifluoromethylpyridines and bis(indolyl)-4-trifluoromethylpyridines were synthesized using Suzuki cross-coupling reaction between 2-chloro-4-trifluoromethylpyridine 9, 2,6-dichloro-4-trifluoromethylpyridine 6 or 2,6-dichloro-3-cyano-4-tri

Herbicidal glutaramic acids and derivatives

This invention relates to glutaramic acids and derivatives exhibiting herbicidal activity having the structure STR1 wherein A is a carboxylic acid or a derivative thereof, D is CH or N, and R, R1, R2, T, X, Y, and Z are as defined within, compositions containing these compounds and methods of controlling weeds with these compounds.