188611

Sigma-Aldrich

3-[2-(Diethylamino)ethyl]-7-hydroxy-4-methylcoumarin hydrochloride

Empirical Formula (Hill Notation):
C16H21NO3 · HCl
CAS Number:
Molecular Weight:
311.80
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22
Pricing and availability is not currently available.

Quality Level

mp

284-287 °C (dec.) (lit.)

SMILES string

Cl[H].CCN(CC)CCC1=C(C)c2ccc(O)cc2OC1=O

InChI

1S/C16H21NO3.ClH/c1-4-17(5-2)9-8-14-11(3)13-7-6-12(18)10-15(13)20-16(14)19;/h6-7,10,18H,4-5,8-9H2,1-3H3;1H

InChI key

RLJNKMCFVQMDFR-UHFFFAOYSA-N

Application

3-[2-(Diethylamino)ethyl]-7-hydroxy-4-methylcoumarin hydrochloride was used in the synthesis of:
  • novel metal-free and zinc phthalocyanines with four 3-[(2-diethylamino)ethyl]-7-oxo-4-methylcoumarin dye groups via cyclotetramerization
  • 3-(2-diethylaminoethyl)-4-methyl-7-substituted coumarins, having antifungal activities against Botrytis cinerea

Packaging

1 g in glass bottle

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Target Organs

Respiratory system

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

RIDADR

NONH for all modes of transport

WGK Germany

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Synthesis and characterization of novel phthalocyanines bearing quaternizable coumarin.
Cakici H, et al.
Polyhedron, 27(18), 3625-3630 (2008)
Synthesis and in vitro evaluation of novel 1, 2, 4-triazole derivatives as antifungal agents.
Kokil GR, et al.
Letters in Drug Design & Discovery, 7(1), 46-49 (2010)
Doyoung Kwon et al.
Molecular pharmacology, 96(5), 641-654 (2019-09-08)
The hepatic endoplasmic reticulum (ER)-anchored monotopic proteins, cytochromes P450 (P450s), are enzymes that metabolize endobiotics (physiologically active steroids and fatty acids), as well as xenobiotics including therapeutic/chemotherapeutic drugs, nutrients, carcinogens, and toxins. Alterations of hepatic P450 content through synthesis, inactivation...
Gönül Yenilmez Çiftçi et al.
Journal of fluorescence, 25(6), 1819-1830 (2015-10-01)
In the present work, 3-[2-(diethylamino)ethyl]-7-oxy-4-methylcoumarin substituted cyclotriphosphazene (4) and cyclotetraphosphazene (5) derivatives were synthesized by the reactions of hexachlorocyclotriphosphazene (1) or octachlorocyclotetraphosphazene (2) with 3-[2-(diethylamino)ethyl]-7-hydroxy-4-methylcoumarin (3) for the first time. The quaternized cationic (6 and 7) and zwitterionic (8 and...

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