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C19H12ClFO is a chemical compound with the molecular formula indicating it contains 19 carbon atoms, 12 hydrogen atoms, 1 chlorine atom, 1 fluorine atom, and 1 oxygen atom. C19H12ClFO likely belongs to a class of organic molecules, possibly with a complex structure given the number of carbon atoms. It may exhibit properties influenced by the presence of a halogen (chlorine) and a heteroatom (oxygen), which can affect its reactivity, solubility, and other physical and chemical characteristics. The specific properties and applications of C19H12ClFO would depend on its exact structure, which is not provided in the molecular formula alone.

441-20-3

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441-20-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 441-20-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,4 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 441-20:
(5*4)+(4*4)+(3*1)+(2*2)+(1*0)=43
43 % 10 = 3
So 441-20-3 is a valid CAS Registry Number.

441-20-3Downstream Products

441-20-3Relevant academic research and scientific papers

Synthesis of new 3-(4-fluoronaphthyl)-5-(aryl)-2-isoxazolines and their antimicrobial and spermicidal activity

Sharma, Sharda,Pathak, Late V. N.,Madan, Harsha,Sharma, Arvind

scheme or table, p. 337 - 340 (2011/12/22)

Microwave assisted synthesis of 3-(4-fluoronaphthyl)-5-(aryl)-2- isoxazolines (3) from corresponding chalcones (2) and hydroxylamine hydrochloride has been accomplished. Structures of synthesized compounds have been confirmed on the basis of spectral studies (IR, 1H NMR) and analytical data. Representative compounds have been screened for their spermicidal activity in HF cattle and were also evaluated for their antibacterial activity against Staphylococcus aureus, E coli, Pseudomonas and antifungal activity against Candida albicans, Asperigillus niger, Fusarium oxysporum.

Solvent free synthesis of new-1-acetyl-3-(4-fluoronaphthyl)-5-substituted aryl pyrazolines as spermicides

Sharma, Sharda,Sharma, Arvind

scheme or table, p. 750 - 753 (2009/12/07)

In this paper we wish to report the solvent free synthesis of 1-acetyl-3-(4-fluoronaphthyl)-5-substituted aryl pyrazolines by using simple and efficient Green Chemistry techniques (Grindstone method and microwave irradiation). These methods have been developed for the rapid solvent free synthesis of title compounds from corresponding chalcones and hydrazine hydrate or phenylhydrazine in acetic acid. Considerable increase in the reaction rates have been observed with better yields compared with sample prepared from conventional method. Structure of synthesized new compounds have been confirmed on the basis of spectral (IR, 1H NMR) and analytical data. Representative compounds have been screened for their spermicidal activity in HF catties and Murrah buffalo.

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