Ethyl nitroacetate

Ethyl nitroacetate Basic information
Product Name:Ethyl nitroacetate
Synonyms:Ethyl nitroacetate 97%;Ethyl nitroacetate,98%;2-Nitroacetic Acid Ethyl Ester;NSC 42302;Ethyl nitrocetate;Nitroacetic acid ethyl ester, Ethyl 2-nitroethanoate;Ethyl nitroacetate, 95+%;Acetic Acid Nitro Ethyl Ester
CAS:626-35-7
MF:C4H7NO4
MW:133.1
EINECS:210-944-7
Product Categories:Halogenated Heterocycles ,Quinolines;C2 to C5;Carbonyl Compounds;Esters
Mol File:626-35-7.mol
Ethyl nitroacetate Structure
Ethyl nitroacetate Chemical Properties
Boiling point 105-107 °C/25 mmHg (lit.)
density 1.199 g/mL at 25 °C (lit.)
refractive index n20/D 1.424(lit.)
Fp 198 °F
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
form Liquid
pkapK1:5.85 (25°C)
color Clear colorless to slightly yellow
Water Solubility Slightly soluble in water. Soluble in chloroform and ethyl acetate.
BRN 1210027
InChIKeyFTKASJMIPSSXBP-UHFFFAOYSA-N
CAS DataBase Reference626-35-7(CAS DataBase Reference)
NIST Chemistry ReferenceAcetic acid, nitro-, ethyl ester(626-35-7)
EPA Substance Registry SystemAcetic acid, nitro-, ethyl ester (626-35-7)
Safety Information
Hazard Codes Xi
Risk Statements 38
Safety Statements 23-24/25-37
WGK Germany 2
RTECS AJ1074000
Hazard Note Irritant
TSCA T
HazardClass IRRITANT, KEEP COLD
HS Code 29159080
MSDS Information
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Ethyl nitroacetate English
SigmaAldrich English
ACROS English
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Ethyl nitroacetate Usage And Synthesis
Chemical Propertiesclear colourless to slightly yellow liquid
UsesEthyl Nitroacetate is an ester of nitrocarboxylic acid used as an intermediate in the preparation of unsubstituted amino acids.
UsesEthyl nitroacetate has been used in the synthesis of γ-oxoacids via Michael addition reaction with α,β-unsaturated ketones, fuctionalization of C4-position on pyrimidine and C6-position on 2?-deoxyguanosine to produce novel nucleosides, facile synthesis of α,α-diisobutylglycine, synthesis of DL-4,4-difluoroglutamic acid. It is also used as an intermediate in the preparation of unsubstituted amino acids.
Synthesis Reference(s)The Journal of Organic Chemistry, 59, p. 1208, 1994 DOI: 10.1021/jo00084a047
Purification MethodsPurify the ester by repeated distillation. IR:max 1748 (CO2), 1570 and 1337 (NO2), and 800cm-1 [Haszeldine J Chem Soc 2525 1953]. The hydrazine salt crystallises from 95% EtOH or MeOH as yellow crystals m 104-105o [Ungnade & Kissinger J Org Chem 22 1661 1957, Emmons & Freeman J Am Chem Soc 77 4391 1955]. [Beilstein 2 IV 537.]
Tetramethylammonium nitrate Cupric nitrate trihydrate Cadmium diethyldithiocarbamate ALFA-NITRO ACETIC ACID AKOS BB-9225 ETHYL 3-AMINO-3-BENZAMIDO-2-NITRO-2-PROPENOATE AURORA KA-5313 AURORA KA-5262 AURORA KA-6068 ISOXADIFEN-ETHYL BIS(2,4-DINITROPHENYL)ACETIC ACID ETHYL ESTER ETHYL 2-NITROBUTYRATE SALOR-INT L160695-1EA 2-CHLORO-2-HYDROXYIMINOACETIC ACID ETHYL ESTER CBI-BB ZERO/001250 4-HYDROXY-6-METHYL-3-NITRO-2H-PYRANO[3,2-C]QUINOLINE-2,5(6H)-DIONE CBI-BB ZERO/008227 AURORA KA-4526

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