38440-12-9 Usage
Molecular weight
176.63 g/mol
Explanation
The molecular weight is the mass of one mole of a substance, expressed in grams per mole (g/mol). For 1,3-Butanedione, 1-(3-chloro-4-fluorophenyl)-, it is 176.63 g/mol.
Explanation
The compound is a type of ketone with a carbonyl group (C=O) and a phenyl ring (C6H5). The phenyl ring has a chlorine atom at the 3rd position and a fluorine atom at the 4th position, making it a substituted aromatic ketone.
Explanation
The two main functional groups in 1,3-Butanedione, 1-(3-chloro-4-fluorophenyl)- are the carbonyl group, which is responsible for the ketone character, and the phenyl group, which is an aromatic ring.
Explanation
The compound contains two halogen atoms, chlorine and fluorine, which are attached to the phenyl ring.
Explanation
Due to its unique structure, 1,3-Butanedione, 1-(3-chloro-4-fluorophenyl)is used as a starting material or intermediate in the synthesis of various compounds, including those used in the pharmaceutical and agrochemical industries.
Explanation
The properties and applications of 1,3-Butanedione, 1-(3-chloro-4-fluorophenyl)- can differ based on the industry in which it is used. For example, it may have different reactivity, stability, or solubility properties in pharmaceutical synthesis compared to agrochemical synthesis.
Explanation
As a substituted aromatic ketone, 1,3-Butanedione, 1-(3-chloro-4-fluorophenyl)- can participate in various chemical reactions, such as electrophilic aromatic substitution, nucleophilic addition, and reduction, among others.
Explanation
Due to its nonpolar nature, 1,3-Butanedione, 1-(3-chloro-4-fluorophenyl)is likely to be soluble in organic solvents like dichloromethane, ethyl acetate, and acetone.
Explanation
The compound is generally stable under normal conditions, such as room temperature and pressure, and in the absence of strong acids, bases, or oxidizing agents. However, it may decompose or react under extreme conditions or in the presence of specific reagents.
Chemical structure
Substituted aromatic ketone
Functional groups
Carbonyl (C=O) and phenyl (C6H5)
Halogen atoms
Chlorine (Cl) and Fluorine (F)
Applications
Building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds
Industry-specific properties
Varies depending on the specific field and industry
Reactivity
Can undergo various chemical reactions
Solubility
Soluble in organic solvents
Stability
Stable under normal conditions
Check Digit Verification of cas no
The CAS Registry Mumber 38440-12-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,4,4 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 38440-12:
(7*3)+(6*8)+(5*4)+(4*4)+(3*0)+(2*1)+(1*2)=109
109 % 10 = 9
So 38440-12-9 is a valid CAS Registry Number.