443697
Ethyl 3-amino-4,4,4-trifluorocrotonate
96%
Synonym(s):
Ethyl 3-amino-4,4,4-trifluoro-2-butenoate
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Linear Formula:
CF3C(NH2)=CHCO2C2H5
CAS Number:
Molecular Weight:
183.13
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Recommended Products
Assay
96%
form
liquid
refractive index
n20/D 1.424 (lit.)
bp
83 °C/15 mmHg (lit.)
density
1.245 g/mL at 25 °C (lit.)
SMILES string
CCOC(=O)C=C(N)C(F)(F)F
InChI
1S/C6H8F3NO2/c1-2-12-5(11)3-4(10)6(7,8)9/h3H,2,10H2,1H3
InChI key
NXVKRKUGIINGHD-UHFFFAOYSA-N
General description
Ethyl 3-amino-4,4,4-trifluorocrotonate is an ester.
Application
Ethyl 3-amino-4,4,4-trifluorocrotonate may be employed for the preparation of 4-trifluoromethyl-1,3-oxazin-6-ones and 4-quinolinone derivatives.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
149.0 °F - closed cup
Flash Point(C)
65 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
新产品
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Aliphatic fluorine-containing amino acids.
Kukhar VP and Soloshonok VA.
Russ. Chem. Rev., 60(8), 850-850 (1991)
Journal of Heterocyclic Chemistry, 30, 49-49 (1993)
Journal of Heterocyclic Chemistry, 30, 71-71 (1993)
Syntheses of New 4-Trifluoromethylated 1, 3-Oxazin-6-Ones from the Enamine of Ethyl Trifluoroacetoacetate.
Decock-Plancquaert M-a, et al.
Bull. Soc. Chim. Belg., 101(4), 313-321 (1992)
A convenient route to diverse heterocycles through an addition of ?-amino carbonyl compounds to 3-halogeno-4-methoxybenzynes.
Yoon K, et al.
The Journal of Organic Chemistry, 70(14), 5741-5744 (2015)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service