Identification | More | [Name]
Diethyl ethoxymethylenemalonate | [CAS]
87-13-8 | [Synonyms]
1,1-DICARBETHOXY-2-ETHOXYETHYLENE 2,2-DICARBETHOXYVINYL ETHYL ETHER AKOS BBS-00004230 DIETHYL ETHOXYMETHYLENEMALONATE EMME ETHOXYMETHYLENEMALONIC ACID DIETHYL ESTER (Ethoxymethylene)-propanedioic acid diethyl ester ETHOXYMETHYLENMALONIC ACID DIETHYL ESTER ETHYL 3-ETHOXY-2-(ETHOXYCARBONYL)ACRYLATE ETHYL A-CARBETHOXY-B-ETHOXYACRYLATE ETHYL ETHOXYMETHYLENE MALONATE LABOTEST-BB LT02094814 (ethoxymethylene)-malonicacidiethylester (ethoxymethylene)-propanedioicacidiethylester Diethyl 2-(ethoxymethylene)malonate diethylemme ethoxymethylenemalonicacid,ethylester Malonic acid, (ethoxymethylene)-, diethyl ester Propanedioicacid,(ethoxymethylene)-,diethylester tl1483 | [EINECS(EC#)]
201-725-7 | [Molecular Formula]
C10H16O5 | [MDL Number]
MFCD00009148 | [Molecular Weight]
216.23 | [MOL File]
87-13-8.mol |
Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
R22:Harmful if swallowed. R36/37/38:Irritating to eyes, respiratory system and skin . R42/43:May cause sensitization by inhalation and skin contact . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . S27:Take off immediately all contaminated clothing . S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
1
| [RTECS ]
OO1100000
| [Autoignition Temperature]
215 °C | [TSCA ]
Yes | [HS Code ]
29189090 | [Safety Profile]
Moderately toxic by
ingestion. A skin irritant. A combustible
liquid. When heated to decomposition it
emits acrid smoke and irritating fumes. | [Toxicity]
LD50 orally in Rabbit: 925 mg/kg LD50 dermal Rat > 2000 mg/kg |
Raw materials And Preparation Products | Back Directory | [Raw materials]
Triethyl orthoformate-->Diethyl malonate | [Preparation Products]
Norfloxacin-->Alachlor-->Lomefloxacin-->Orotic acid-->ETHYL 4-CHLORO-3-METHYLTHIENO[2,3-B]PYRIDINE-5-CARBOXYLATE-->Ethyl 4-chloro-2-(trifluoromethyl)pyrimidine-5-carboxylate-->ETHYL 4-AMINO-2-(METHYLTHIO)PYRIMIDINE-5-CARBOXYLATE-->Ethyl 4-chloro-2-methylthio-5-pyrimidinecarboxylate-->5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4(3H)-one-->Levofloxacin-->7-TRIFLUOROMETHYL-4-QUINOLINETHIOL-->1,4-DIHYDRO-2-(METHYLTHIO)-4-OXO-5-PYRIMIDINE-CARBOXYLATE ACID ETHYL ESTER-->7-BROMO-3,4-DIHYDRO-4-OXOQUINOLINE-3-CARBOXYLIC ACID-->7-(TRIFLUOROMETHYL)-4-QUINOLINOL-->4-HYDROXY-7-TRIFLUOROMETHYL-3-QUINOLINECARBOXYLIC ACID-->Fleroxacin-->4-HYDROXY-2-METHYL-PYRIMIDINE-5-CARBOXYLIC ACID ETHYL ESTER-->Nalidixic acid-->ETHYL 4-CHLOROTHIENO[2,3-B]PYRIDINE-5-CARBOXYLATE-->4-HYDROXY-2-PHENYL-5-PYRIMIDINECARBOXYLIC ACID-->3,4-DIHYDRO-8-HYDROXY-4-OXOQUINOLINE-3-CARBOXYLIC ACID-->Ethyl 7-bromo-3,4-dihydro-4-oxoquinoline-3-carboxylate ,97%-->4-AMINO-2-METHYLSULFANYL-PYRIMIDINE-5-CARBOXYLIC ACID-->4-HYDROXY-8-METHOXYQUINOLINE-3-CARBOXYLIC ACID-->6-CHLORO-[1,2,4]TRIAZOLO[4,3-B]PYRIDAZINE-->ETHYL 4-HYDROXY-7-(TRIFLUOROMETHYL)QUINOLINE-3-CARBOXYLATE-->Ethyl 4-hydroxy-2-phenylpyrimidine-5-carboxylate-->Decoquinate-->4-HYDROXY-8-METHOXY-QUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER |
Hazard Information | Back Directory | [Chemical Properties]
CLEAR COLOURLESS TO LIGHT YELLOW LIQUID | [Uses]
Intermediate in the production of Flumequine | [Purification Methods]
Likely impurity is diethyl diethoxymethylene malonate which is difficult to separate from diethyl ethoxymethylene malonate by distillation, and it is necessary to follow the course of the distillation by the change in refractive index instead of boiling point. After a low boiling fraction is collected, there is obtained an intermediate fraction (n 20 1.414—1.458), the size of which depends on the amount of the diethoxymethylene compound. This fraction is fractionated through a 5inch Vigreux column (p 11) at low pressure avoiding interruption in heating. Fraction b 108-110o/0.25mm is ca 10o lower than the submitters' fraction (b 97.2o/0.25mm, n D 1.4612—1.4623) [Org Synth Coll Vol III 395 1955, Fuson et al. J Org Chem 11 197 1946, Duff & Kendal J Chem Soc 893 1948]. [Beilstein 3 IV 1192.] |
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