5828-09-1 Usage
Appearance
Colorless to pale yellow liquid
The physical state and color of the compound, which can range from transparent to slightly colored.
Odor
Pungent
The compound has a strong, irritating smell that can be detected easily.
Usage in pharmaceuticals and pesticides
Common
The compound is frequently used as a starting material or intermediate in the synthesis of various drugs and pest control agents.
Flavoring agent
Food industry, particularly fruit flavors
It is used to impart specific tastes and aromas to food products, mainly those with fruity notes.
Application in organic synthesis
Synthesis of various organic chemicals
The compound serves as a reactant or building block in the creation of other organic molecules.
Use in rubber production
Component in rubber products
It may be used as a component or additive to modify the properties of rubber materials.
Safety concerns
Harmful if ingested or inhaled
The compound poses potential health risks when swallowed or breathed in, necessitating proper handling and safety precautions.
Check Digit Verification of cas no
The CAS Registry Mumber 5828-09-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,2 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5828-09:
(6*5)+(5*8)+(4*2)+(3*8)+(2*0)+(1*9)=111
111 % 10 = 1
So 5828-09-1 is a valid CAS Registry Number.
5828-09-1Relevant articles and documents
1,3-Carbonyl transposition methodology employing α-oxo ketene dithioacetals: Application in the synthesis of phenols and (±)-myodesmone
Dieter,Lin,Dieter
, p. 3183 - 3195 (2007/10/02)
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α-OXOKETENE DITHIOACETALS: VERSATILE SUBSTRATES FOR 1,3-CARBONYL TRANSPOSITIONS
Dieter, R. Karl,Jenkitkasemwong, Yawares
, p. 3747 - 3750 (2007/10/02)
A two step procedure for the conversion of α-oxoketene dithioacetals to β-substituted α,β-unsaturated thioesters or acids is described.The overall transformation represents a 1,3-carbonyl transposition in which the original ketone carbonyl emerges as the carbonyl of an acid or thioester.The resulting thioesters and acids constitute versatile acylating reagents in accord with established procedures.
