Welcome to LookChem.com Sign In|Join Free
  • or
1,3-Butanedione, 1-(3-chloro-4-fluorophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38440-12-9

Post Buying Request

38440-12-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

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.

38440-12-9Relevant academic research and scientific papers

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 38440-12-9