ChemicalBook > Product Catalog > Chemical Reagents > Organic reagents > Phosphonate / phosphonate > TRIETHYL 4-PHOSPHONOCROTONATE
TRIETHYL 4-PHOSPHONOCROTONATE
TRIETHYL 4-PHOSPHONOCROTONATE Basic information
- Product Name:
- TRIETHYL 4-PHOSPHONOCROTONATE
- Synonyms:
-
- 4-PHOSPHONOCROTONIC ACID TRIETHYL ESTER
- TRANS-ETHYL-4-(DIETHYLPHOSPHONO)CROTONATE
- TRIETHYL 4-PHOSPHONO-2-BUTENOATE
- TRIETHYL 4-PHOSPHONOCROTONATE
- TRIETHYL 4-PHOSPHONOCROTONATE, TECH., 90 %, MIXTURE OF ISOMERS
- Triethyl 4-phosphonocrotonate, predominantly trans, 92%
- triethyl 4-phosphonocrotonate, cis + trans
- triethyl 4-phosphonocrotonate, mixture of isomers
- CAS:
- 10236-14-3
- MF:
- C10H19O5P
- MW:
- 250.23
- Product Categories:
-
- C-C Bond Formation
- Horner-Wadsworth-Emmons Reagents
- Olefination
- Mol File:
- 10236-14-3.mol
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TRIETHYL 4-PHOSPHONOCROTONATE Chemical Properties
- Boiling point:
- 135 °C0.4 mm Hg(lit.)
- Density
- 1.128 g/mL at 25 °C(lit.)
- refractive index
- n20/D 1.455(lit.)
- Flash point:
- >230 °F
- form
- Liquid
- color
- Clear light yellow
- CAS DataBase Reference
- 10236-14-3(CAS DataBase Reference)
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Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38
- Safety Statements
- 26-37/39-24/25
- WGK Germany
- 3
- HazardClass
- IRRITANT
- HS Code
- 29319090
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
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TRIETHYL 4-PHOSPHONOCROTONATE Usage And Synthesis
Chemical Properties
CLEAR LIGHT YELLOW LIQUID
Uses
Triethyl 4-phosphonocrotonate is used as a reactant for iminodipropionic acid as a leaving group for DNA polymerization by HIV-1 reverse transcriptase, orally bioavailable GPR40 agonist synthesis, preparation of mGlu4R agonists and synthesis of fluoroketone inhibitors of group VIA calcium-independent phospholipase A2.
Uses
Reactant for:
- Iminodipropionic acid as a leaving group for DNA polymerization by HIV-1 reverse transcriptase
- Stereoselective preparation of C1-C19 fragment of macrolide antibiotic aplyronine A using diastereoselective Nozaki-Hiyama-Kishi coupling reactions
- Orally bioavailable GPR40 agonist synthesis
- Synthesis of fluoroketone inhibitors of group VIA calcium-independent phospholipase A2
- Preaparation of mGlu4R agonists
- Dearomatizing cyclization of nicotinyl-substituted esters and ketones
TRIETHYL 4-PHOSPHONOCROTONATESupplier
J & K SCIENTIFIC LTD.
- Tel
- 010-82848833 400-666-7788
- jkinfo@jkchemical.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
- Tel
- 021-61259108 18621169109
- market03@meryer.com
Alfa Aesar
- Tel
- 400-6106006
- saleschina@alfa-asia.com
Energy Chemical
- Tel
- 021-021-58432009 400-005-6266
- sales8178@energy-chemical.com
Shanghai Hanhong Scientific Co.,Ltd.
- Tel
- 021-54306202 13764082696
- info@hanhongsci.com
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TRIETHYL 4-PHOSPHONOCROTONATE(10236-14-3)Related Product Information
- TRIETHYL 4-PHOSPHONOBUTYRATE
- TRIETHYL 3-PHOSPHONOPROPIONATE
- Dimethyl methylphosphonate
- DIMETHYL ETHYLPHOSPHONATE
- DIETHYL ALLYLPHOSPHONATE
- Methyldiethoxyphosphine
- DIMETHYL ALLYLPHOSPHONATE
- ETHYL METHYLPHOSPHONIC ACID
- METHYLPHOSPHONIC ACID
- ETHYLPHOSPHONIC ACID
- TRIETHYL 4-PHOSPHONOCROTONATE
- DIMETHYL ETHYLPHOSPHONITE
- DIETHYL ETHYLPHOSPHONATE
- Diethyl methylphosphonate
- TRIMETHYL 4-PHOSPHONOCROTONATE
- TRIETHYL 3-METHYL-4-PHOSPHONOCROTONATE
- ETHYL HYDROGEN ETHYLPHOSPHONATE
- ALLYLPHOSPHONIC ACID