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3-FORMYL-6-METHYLCHROMONE

Product Name
3-FORMYL-6-METHYLCHROMONE
CAS No.
42059-81-4
Chemical Name
3-FORMYL-6-METHYLCHROMONE
Synonyms
IFLAB-BB F2121-0035;3-FORMYL-6-METHYLCHROMONE;6-Methyl-3-formyl chromone;3-Formyl-6-methylchromone,97%;3-Formyl-6-methoxy-4-chromanone;6-Methylchromone-3-carboxaldehyde;6-methyl-4-oxochromene-3-carbaldehyde;6-methyl-4-oxo-chromene-3-carbaldehyde;6-methyl-4-oxo-3-chromenecarboxaldehyde;4-keto-6-methyl-chromene-3-carbaldehyde
CBNumber
CB4694739
Molecular Formula
C11H8O3
Formula Weight
188.18
MOL File
42059-81-4.mol
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3-FORMYL-6-METHYLCHROMONE Property

Melting point:
172-173 °C (lit.)
Boiling point:
335.1±42.0 °C(Predicted)
Density 
1.47 g/cm3
storage temp. 
Inert atmosphere,Room Temperature
form 
powder to crystal
color 
White to Yellow to Green
λmax
308nm(Dioxane)(lit.)
InChIKey
GBWMIOYSMWCYIZ-UHFFFAOYSA-N
CAS DataBase Reference
42059-81-4(CAS DataBase Reference)
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Safety

Hazard Codes 
Xi
Safety Statements 
24/25
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29329990
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
383473
Product name
3-Formyl-6-methylchromone
Purity
97%
Packaging
5g
Price
$84.3
Updated
2024/03/01
TCI Chemical
Product number
F1005
Product name
3-Formyl-6-methylchromone
Purity
>98.0%(GC)
Packaging
1g
Price
$23
Updated
2024/03/01
TCI Chemical
Product number
F1005
Product name
3-Formyl-6-methylchromone
Purity
>98.0%(GC)
Packaging
5g
Price
$50
Updated
2024/03/01
TRC
Product number
M325408
Product name
6-Methyl-4-oxo-4H-chromene-3-carbaldehyde
Packaging
100mg
Price
$60
Updated
2021/12/16
AK Scientific
Product number
3045AE
Product name
6-Methyl-4-oxo-4H-chromene-3-carbaldehyde
Packaging
25g
Price
$49
Updated
2021/12/16
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3-FORMYL-6-METHYLCHROMONE Chemical Properties,Usage,Production

Chemical Properties

yellow powder

Uses

3-Formyl-6-methylchromone may be used in the preparation of series of Schiff′s bases, via reaction with aromatic sulfonamides, such as sulfanilamide, homosulfanilamide, 4-aminoethyl-benzenesulfonamide, a pyrimidinyl-substituted sulfanilamide derivative, sulfaguanidine and 4-amino-6-trifluoromethyl-benzene-1,3-disulfonamide. It may be used in the preparation of Schiff base, which undergoes addition reaction with diethyl phosphite to afford bis[(1,2,4,3-triazaphospholyl)(chromonyl)aminomethylphosphonate] derivative and bis[(1,2,4,3-triazaphospholyl)(chromonyl)phosphorylamino-methylphosphonate] derivative.

General Description

3-Formyl-6-methylchromone is a 3-formyl-substituted chromone. The combustion calorimetric estimation of the enthalpy of combustion of 3-formyl-6-methylchromone has been reported. Its anti-proliferative action on the MDR human colon cancer and mouse lymphoma has been investigated.

3-FORMYL-6-METHYLCHROMONE Preparation Products And Raw materials

Raw materials

Preparation Products

42059-81-4, 3-FORMYL-6-METHYLCHROMONERelated Search:


  • IFLAB-BB F2121-0035
  • 3-Formyl-6-methylchromone,97%
  • 6-methyl-4-oxo-3-chromenecarboxaldehyde
  • 6-methyl-4-oxo-chromene-3-carbaldehyde
  • 6-methyl-4-oxochromene-3-carbaldehyde
  • 6-Methyl-4-oxo-(4H)-1-benzopyrane-3-carboxaldehyde
  • 4H-1-benzopyran-3-carboxaldehyde, 6-methyl-4-oxo-
  • 4-keto-6-methyl-chromene-3-carbaldehyde
  • 3-FORMYL-6-METHYLCHROMONE
  • 6-METHYL-4-OXO-4 H-1-BENZOPYRAN-3-CARBOXALDEHYDE
  • 6-METHYL-4-OXO-4H-CHROMENE-3-CARBALDEHYDE
  • 4-fluorobenzoic acid [2-oxo-2-[3-(trifluoromethyl)anilino]ethyl] ester
  • JRH-00102, 6-Methyl-4-oxo-4H-chromene-3-carbaldehyde, 97%
  • 3-Formyl-6-methoxy-4-chromanone
  • 6-Methylchromone-3-carboxaldehyde
  • 6-Methyl-3-formyl chromone
  • 42059-81-4
  • ALDEHYDE
  • Heterocyclic Building Blocks
  • Benzopyrans
  • Building Blocks
  • Aldehydes
  • Benzopyrans
  • Building Blocks
  • C10-C12
  • Carbonyl Compounds
  • Chemical Synthesis
  • Heterocyclic Building Blocks
  • Organic Building Blocks
  • Chromones