13081-18-0,MFCD00114935
Catalog No.:AA0034U8

13081-18-0 | Ethyl trifluoropyruvate

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
98%
in stock  
$6.00   $4.00
- +
10g
98%
in stock  
$7.00   $5.00
- +
25g
98%
in stock  
$16.00   $11.00
- +
100g
95%
in stock  
$62.00   $44.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0034U8
Chemical Name:
Ethyl trifluoropyruvate
CAS Number:
13081-18-0
Molecular Formula:
C5H5F3O3
Molecular Weight:
170.0866
MDL Number:
MFCD00114935
SMILES:
CCOC(=O)C(=O)C(F)(F)F
Properties
Properties
 
BP:
58.5°C at 760 mmHg  
Form:
Liquid  
Refractive Index:
n20/D 1.341(lit.)  
Solubility:
Miscible with dichloromethane.  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
172  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
6  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
3  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
1.5  

Literature

Title: Asymmetric synthesis of the carbon-14-labeled selective glucocorticoid receptor modulator using cinchona alkaloid catalyzed addition of 6-bromoindole to ethyl trifluoropyruvate.

Journal: Molecules (Basel, Switzerland) 20120530

Title: Ethyl 3,3,3-trifluoro-2-hy-droxy-2-(5-meth-oxy-1H-indol-3-yl)propionate.

Journal: Acta crystallographica. Section E, Structure reports online 20110701

Title: Straightforward synthesis of enantiopure (R)- and (S)-trifluoroalaninol.

Journal: Organic & biomolecular chemistry 20101021

Title: Joint experimental and DFT study of the gas-phase unimolecular elimination kinetic of methyl trifluoropyruvate.

Journal: The journal of physical chemistry. A 20100805

Title: Catalytic asymmetric synthesis of 3-(alpha-hydroxy-beta-carbonyl) oxindoles by a Sc(III)-catalyzed direct aldol-type reaction.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20100322

Title: The first organocatalytic carbonyl-ene reaction: isomerisation-free C-C bond formations catalysed by H-bonding thio-ureas.

Journal: Beilstein journal of organic chemistry 20070101

Title: Cinchona-alkaloid-catalyzed enantioselective direct aldol-type reaction of oxindoles with ethyl trifluoropyruvate.

Journal: Angewandte Chemie (International ed. in English) 20070101

Title: Asymmetric platinum group metal-catalyzed carbonyl-ene reactions: carbon-carbon bond formation versus isomerization.

Journal: The Journal of organic chemistry 20061222

Title: Straightforward synthesis of (S)- and (R)-alpha-trifluoromethyl proline from chiral oxazolidines derived from ethyl trifluoropyruvate.

Journal: Organic letters 20061221

Title: Highly enantioselective organocatalytic hydroxyalkylation of indoles with ethyl trifluoropyruvate.

Journal: Angewandte Chemie (International ed. in English) 20050513

Title: Regioselectively nucleus and/or side-chain fluorinated 2-(Phenanthryl)propionic acids by an effective combination of radical and organometallic chemistry.

Journal: The Journal of organic chemistry 20050121

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SDS
Tags:13081-18-0 Molecular Formula|13081-18-0 MDL|13081-18-0 SMILES|13081-18-0 Ethyl trifluoropyruvate
Catalog No.: AA0034U8
13081-18-0,MFCD00114935
13081-18-0 | Ethyl trifluoropyruvate
Pack Size: 5g
Purity: 98%
in stock
$6.00 $4.00
Pack Size: 10g
Purity: 98%
in stock
$7.00 $5.00
Pack Size: 25g
Purity: 98%
in stock
$16.00 $11.00
Pack Size: 100g
Purity: 95%
in stock
$62.00 $44.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA0034U8
Chemical Name: Ethyl trifluoropyruvate
CAS Number: 13081-18-0
Molecular Formula: C5H5F3O3
Molecular Weight: 170.0866
MDL Number: MFCD00114935
SMILES: CCOC(=O)C(=O)C(F)(F)F
Properties
BP: 58.5°C at 760 mmHg  
Form: Liquid  
Refractive Index: n20/D 1.341(lit.)  
Solubility: Miscible with dichloromethane.  
Storage: Inert atmosphere;2-8℃;  
Complexity: 172  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 11  
Hydrogen Bond Acceptor Count: 6  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 3  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 1.5  
Literature fold

Title: Asymmetric synthesis of the carbon-14-labeled selective glucocorticoid receptor modulator using cinchona alkaloid catalyzed addition of 6-bromoindole to ethyl trifluoropyruvate.

Journal: Molecules (Basel, Switzerland)20120530

Title: Ethyl 3,3,3-trifluoro-2-hy-droxy-2-(5-meth-oxy-1H-indol-3-yl)propionate.

Journal: Acta crystallographica. Section E, Structure reports online20110701

Title: Straightforward synthesis of enantiopure (R)- and (S)-trifluoroalaninol.

Journal: Organic & biomolecular chemistry20101021

Title: Joint experimental and DFT study of the gas-phase unimolecular elimination kinetic of methyl trifluoropyruvate.

Journal: The journal of physical chemistry. A20100805

Title: Catalytic asymmetric synthesis of 3-(alpha-hydroxy-beta-carbonyl) oxindoles by a Sc(III)-catalyzed direct aldol-type reaction.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany)20100322

Title: The first organocatalytic carbonyl-ene reaction: isomerisation-free C-C bond formations catalysed by H-bonding thio-ureas.

Journal: Beilstein journal of organic chemistry20070101

Title: Cinchona-alkaloid-catalyzed enantioselective direct aldol-type reaction of oxindoles with ethyl trifluoropyruvate.

Journal: Angewandte Chemie (International ed. in English)20070101

Title: Asymmetric platinum group metal-catalyzed carbonyl-ene reactions: carbon-carbon bond formation versus isomerization.

Journal: The Journal of organic chemistry20061222

Title: Straightforward synthesis of (S)- and (R)-alpha-trifluoromethyl proline from chiral oxazolidines derived from ethyl trifluoropyruvate.

Journal: Organic letters20061221

Title: Highly enantioselective organocatalytic hydroxyalkylation of indoles with ethyl trifluoropyruvate.

Journal: Angewandte Chemie (International ed. in English)20050513

Title: Regioselectively nucleus and/or side-chain fluorinated 2-(Phenanthryl)propionic acids by an effective combination of radical and organometallic chemistry.

Journal: The Journal of organic chemistry20050121

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