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propyl 4-diethylcarbamoylmethoxy-3-methoxyphenylacetate

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propyl 4-diethylcarbamoylmethoxy-3-methoxyphenylacetate Basic information

Product Name:
propyl 4-diethylcarbamoylmethoxy-3-methoxyphenylacetate
Synonyms:
  • KEJXLQUPYHWCNM-UHFFFAOYSA-N
  • propanidid
  • propyl 4-diethylcarbamoylmethoxy-3-methoxyphenylacetate
  • PROPANIDIDE
  • Bayer-1420
  • Epontol
  • FBA-1420
  • Sombrevin
CAS:
1421-14-3
MF:
C18H27NO5
MW:
337.41
EINECS:
215-822-7
Mol File:
1421-14-3.mol
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propyl 4-diethylcarbamoylmethoxy-3-methoxyphenylacetate Chemical Properties

Boiling point:
bp0.7 210-212°
Density 
1.2043 (rough estimate)
refractive index 
1.5000 (estimate)
storage temp. 
Refrigerator
solubility 
DMSO (Slightly), Ethyl Acetate (Slightly)
form 
Oil
color 
Pale Yellow to Yellow
EPA Substance Registry System
Propanidid (1421-14-3)
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Safety Information

Toxicity
LD50 orally in rats: >10,000 mg/kg (Goldenthal)
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propyl 4-diethylcarbamoylmethoxy-3-methoxyphenylacetate Usage And Synthesis

Chemical Properties

yellow oil bp0.7 210-212°C soluble in alcohol, chloroform, essentially water insoluble anasthetic Epontol (Bayer) Sombrevin

Uses

Anesthetic (intravenous).

Uses

Sombrevin, is an ultra short-acting phenylacetate general anesthetic.

Definition

ChEBI: Propanidid is a member of methoxybenzenes.

brand name

Epontol (Farbenfabriken Bayer A.G., Germany).

Clinical Use

Propanidid is used as a very short- to shortacting intravenous anesthetic for minor surgery and gynecology. It is characterized by rapid onset of and quick recovery from anesthesia, producing surgical anesthesia for 3 – 4 min. Repeated injections can be used to prolong the anesthesia. Postanesthetic sleep does not occur because the propyl ester is hydrolyzed rapidly in the patient to form inactive 3-methoxy-4- (N,N-diethylcarbamoylmethoxy)phenylacetic acid. After 20 – 30 min the patients generally are completely responsive .

Synthesis

Propanidid , propyl 3- methoxy-4-(N,N-diethylcarbamoylmethoxy)- phenylacetate, is a colorless to pale yellowish water-insoluble oil. It is prepared from the propyl ester of sodium homovanillic acid and N,N-diethylchloroacetamide .

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