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Home > Products >  Ethyl Malonyl chloride

Ethyl Malonyl chloride CAS NO.36239-09-5

  • Min.Order: 100 Gram
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  • 36239-09-5
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Quick Details

  • ProName: Ethyl Malonyl chloride
  • CasNo: 36239-09-5
  • Molecular Formula: C5H7ClO3
  • Appearance: white or light yellow crystalline powd...
  • Application: Used for research and industrial manuf...
  • DeliveryTime: Within 3-7 days after receipt of your ...
  • PackAge: As customer request
  • Port: Qingdao,China
  • ProductionCapacity: 100 Metric Ton/Month
  • Purity: 98%min
  • Storage: Store in a cool,dry place and keep awa...
  • Transportation: As customer request
  • LimitNum: 100 Gram

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Details

Details

Product Name: Ethyl malonyl chloride
Synonyms: 3-chloro-3-oxo-propanoicaciethylester;Propanoic acid, 3-chloro-3-oxo-, ethyl ester;MALONIC ACID MONOETHYL ESTER CHLORIDE;AURORA KA-3051;(CHLOROFORMYL)ACETIC ACID ETHYL ESTER;ETHYL 3-CHLORO-3-OXOPROPIONATE;ETHYL 2-(CHLOROCARBONYL)ACETATE;ETHYL MALONYL CHLORIDE
CAS: 36239-09-5
MF: C5H7ClO3
MW: 150.56
EINECS: 252-934-5
Product Categories: Aliphatics;Acid Halides;Building Blocks;Carbonyl Compounds;Chemical Synthesis;Organic Building Blocks;Pharmaceutical raw material;Pharmaceutical intermdiate
Mol File: 36239-09-5.mol
Ethyl malonyl chloride Structure
 
Ethyl malonyl chloride Chemical Properties
bp 79-80 °C25 mm Hg(lit.)
density 1.196 g/mL at 20 °C
refractive index n20/D 1.429(lit.)
Fp 154 °F
storage temp. 2-8°C
Water Solubility REACTS
Sensitive Moisture Sensitive
BRN 636215
CAS DataBase Reference 36239-09-5(CAS DataBase Reference)
NIST Chemistry Reference Ethyl malonyl chloride(36239-09-5)
 
Safety Information
Hazard Codes C
Risk Statements 14-34
Safety Statements 7-26-36/37/39-45-36/39
RIDADR UN 3265 8/PG 3
WGK Germany 3
F 10-21
Hazard Note Corrosive
HazardClass 8
PackingGroup II
MSDS Information
Provider Language
Ethyl (chloroformyl)acetate English
SigmaAldrich English
ACROS English
ALFA English
 
Ethyl malonyl chloride Usage And Synthesis
Chemical Properties clear yellow to brown liquid
Usage Employed in the synthesis of 3-pyrrolin-2-ones via amidation with propargylamines and subsequent base catalyzed 5-exo-dig cyclization.1

 

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