Interesting facts
Fascinating Insights into Chromen-2-one
Chromen-2-one, also known as coumarin, is a fascinating compound widely studied for its varied applications in both scientific and commercial fields. Here are some interesting aspects of this aromatic compound:
- Natural Occurrence: Chromen-2-one can be found in many plants, particularly in the essential oils of certain types of herbs like tonka beans and lavender. It is responsible for the characteristic sweet scent in these botanicals.
- Medicinal Properties: The compound has garnered attention in pharmacology due to its potential therapeutic effects, including anti-inflammatory, anticoagulant, and antioxidant properties. This makes it a subject of interest for developing new medications.
- Flavoring Agent: Coumarin is commonly used as a flavor enhancer in food products and fragrances. It adds a sweet, vanilla-like aroma, making it popular in the food industry, especially in confectioneries.
- Chemical Versatility: Chromen-2-one serves as a versatile scaffold in organic synthesis, allowing chemists to create various derivatives that can yield new compounds with useful properties.
- Research and Applications: Ongoing studies are investigating coumarin's potential in treating conditions like cancer, cardiovascular diseases, and even its role as an insect repellent.
In summary, chromen-2-one is more than just a simple chemical structure; it represents a bridge between nature, flavor, and medicine. As scientists continue to explore its properties, we may unlock even more secrets hidden within this intriguing compound.
Synonyms
coumarin
91-64-5
2H-Chromen-2-one
2H-1-Benzopyran-2-one
cumarin
1,2-Benzopyrone
chromen-2-one
Rattex
Coumarinic anhydride
Tonka bean camphor
Coumarine
cis-o-Coumarinic acid lactone
Coumarinic lactone
o-Hydroxycinnamic acid lactone
Benzo-alpha-pyrone
o-Hydroxycinnamic lactone
2-Oxo-1,2-benzopyran
Kumarin
Benzo-a-pyrone
2H-Benzo(b)pyran-2-one
5,6-Benzo-2-pyrone
2H-1-Benzopyran, 2-oxo-
Kumarin [Czech]
o-Hydroxyzimtsaure-lacton
5,6-Benzo-alpha-pyrone
2H-Benzo[b]pyran-2-one
Coumarinum
1-Benzopyran-2-one
NCI C07103
103802-83-1
Caswell No. 259C
o-Coumaric acid lactone
NSC 8774
CCRIS 181
cis-o-Coumaric acid anhydride
chromenone
EPA Pesticide Chemical Code 127301
DTXSID7020348
CHEBI:28794
BRN 0383644
HSDB 1623
2-oxo-2H-1-benzopyran
o-Hydroxyzimtsaure-lacton [German]
AI3-00753
UNII-A4VZ22K1WT
NSC-8774
EINECS 202-086-7
A4VZ22K1WT
Nci-c07103
MFCD00006850
2-Propenoic acid, 3-(2-hydroxyphenyl)-, delta-lactone
3-(2-Hydroxyphenyl)-2-propenoic delta-lactone
Benzo-.alpha.-pyrone
Cinnamic acid, o-hydroxy-, delta-lactone
Coumarin (prohibited)
NSC8774
o-hydroxycinnamic acid delta-lactone
CHEMBL6466
2-Propenoic acid, 3-(2-hydroxyphenyl)-delta-lactone
DTXCID50348
MLS000028741
EC 202-086-7
5-17-10-00143 (Beilstein Handbook Reference)
NCGC00091502-01
Coumarin, >=98%
SMR000059040
COUMARIN (IARC)
COUMARIN [IARC]
COUMARIN (MART.)
COUMARIN [MART.]
2h-chromene-2-one
2-Propenoic acid, 3-(2-hydroxyphenyl)-, d-lactone
2-Propenoic acid, 3-(2-hydroxyphenyl)-, .delta.-lactone
benzopyranone
coumarinac lactone
CAS-91-64-5
Coumarin [NF]
COU
2H-Benzopyran-2-one
SR-01000721887
chromen-one
a coumarin
coumarin-
d-lactone
Venalot mono
Coumarin Phenolic
Rattex Rodenticide
benzopyrylium olate
Coumarin (DCF)
Coumarin1513
1, 2-Benzopyrone
a 1,2-benzopyrone
Coumarin (Standard)
Venalot mono (TN)
Spectrum_001336
ST023509
COUMARIN [HSDB]
Opera_ID_268
2H-Chromen-2-one #
3-(2-hydroxyphenyl)-
COUMARIN [MI]
2H-1-benzopyran-2-on
Spectrum2_000303
Spectrum3_001772
Spectrum4_001818
Spectrum5_000555
COUMARINUM [HPUS]
bmse000077
COUMARIN [WHO-DD]
Epitope ID:114082
SCHEMBL6252
WLN: T66 BOVJ
BSPBio_003263
KBioGR_002460
KBioSS_001816
MLS001148422
MLS002454395
{2H-Benzo[b]pyran-2-one}
BIDD:ER0667
SPECTRUM1400208
SPBio_000266
Cinnamic acid, .delta.-lactone
Coumarin, >=99% (HPLC)
BDBM12342
HY-N0709R
KBio2_001816
KBio2_004384
KBio2_006952
KBio3_002764
GLXC-19130
HMS1923M11
HMS2091E19
HMS2232H18
HMS3369L08
HMS3652B05
HMS3885D09
Pharmakon1600-01400208
HY-N0709
Tox21_111141
Tox21_202427
Tox21_300057
CCG-38580
NSC755852
s4170
STK066167
COUMARIN (PROHIBITED) [FHFI]
AKOS000120175
Tox21_111141_1
2H-chromen-2-one (ACD/Name 4.0)
CR-0048
CS-8148
DB04665
FC20572
NSC-755852
SDCCGMLS-0066912.P001
USEPA/OPP Pesticide Code: 127301
NCGC00091502-02
NCGC00091502-03
NCGC00091502-04
NCGC00091502-05
NCGC00091502-06
NCGC00091502-07
NCGC00091502-08
NCGC00091502-09
NCGC00091502-11
NCGC00091502-12
NCGC00091502-16
NCGC00254092-01
NCGC00259976-01
Coumarin 1000 microg/mL in Acetonitrile
NCI60_041938
SBI-0061760.P002
DB-057267
DB-261057
Cinnamic acid, o-hydroxy-, .delta.-lactone
Coumarin, Vetec(TM) reagent grade, >=99%
NS00002381
SW220278-1
EN300-18115
BIM-0061760.0001
C05851
D07751
D81844
AB00375898_11
AB00375898_12
AP-123/40186862
Coumarin, primary pharmaceutical reference standard
Q111812
CU-01000013121-2
SR-01000721887-2
SR-01000721887-3
BRD-K23913458-001-02-5
BRD-K23913458-001-13-2
BRD-K23913458-001-19-9
BRD-K23913458-001-20-7
Coumarin, certified reference material, TraceCERT(R)
Z57169486
Coumarin, European Pharmacopoeia (EP) Reference Standard
F3096-1712
2H-1-Benzopyran-2-one;1,2-Benzopyrone;5,6-Benzo-2-pyrone
COUMARIN (CONSTITUENT OF CINNAMOMUM CASSIA BARK) [DSC]
COUMARIN (CONSTITUENT OF CINNAMOMUM VERUM BARK) [DSC]
D3E956C4-9541-4F57-9435-7D915C38E19E
InChI=1/C9H6O2/c10-9-6-5-7-3-1-2-4-8(7)11-9/h1-6
202-086-7
2h-1-benzopyran-2-one;coumarin;2h-chromen-2-one;coumarin ;coumarin (2h-1-benzopyran-2-one) (chromen-2-one);2h-1-benzopyran-2-one coumarin 2h-chromen-2-one coumarin coumarin (2h-1-benzopyran-2-one) (chromen-2-one)
Solubility of Chromen-2-one (C9H6O2)
Chromen-2-one, also known as coumarin, exhibits interesting solubility characteristics that are largely influenced by its molecular structure. Here are some key points regarding its solubility:
According to some studies, “the solubility behaviors are essential for its applications in pharmaceuticals, fragrances, and flavors due to its key role in delivering desired properties.” Therefore, understanding and manipulating its solubility can significantly impact its utility in various fields.